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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-K
[☒] Annual Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
For the fiscal year ended December 31, 2020
or
[☐] Transition report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
For the transition period from ______ to ______
Commission file number - 1-11353
LABORATORY CORPORATION OF AMERICA HOLDINGS
(Exact name of registrant as specified in its charter)
Delaware
(State or other jurisdiction of incorporation or organization)
13-3757370
(I.R.S. Employer Identification No.)
358 South Main Street
Burlington,
North Carolina
(Address of principal executive offices)
27215
(Zip Code)
(Registrant's telephone number, including area code) 336-229-1127
Securities registered pursuant to Section 12(b) of the Act:
Title of each class
Common Stock, $0.10 par value
Trading Symbol
LH
Securities registered pursuant to Section 12(g) of the Act: None
Name of exchange on which registered
New York Stock Exchange
Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes [X]
No [ ].
Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or 15(d) of the Act. Yes [ ] No [X].
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the
Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to
file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes [X] No [ ].
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted
pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period
that the registrant was required to submit such files). Yes [X] No [ ].
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller
reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,”
“smaller reporting company”, and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large accelerated filer
Non-accelerated filer
☒ Accelerated filer
☐ Smaller reporting company
Emerging growth company
☐
☐
☐
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If emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for
complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. [ ]
Indicate by check mark whether the registrant has filed a report on and attestation to its management's assessment of the
effectiveness of its internal control over financial reporting under Section 404(b) of the Sarbanes-Oxley Act (15 U.S.C.
7262(b)) by the registered public accounting firm that prepared or issued its audit report.
Yes ☒ No [ ].
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act). Yes [☐] No [X].
As of June 30, 2020, the aggregate market value of the common stock held by non-affiliates of the registrant was approximately
$15.2 billion, based on the closing price on such date of the registrant’s common stock on the New York Stock Exchange.
Indicate the number of shares outstanding of each of the registrant's classes of common stock, as of the latest practicable date:
97.6 million shares as of February 24, 2021.
DOCUMENTS INCORPORATED BY REFERENCE
List hereunder the following documents if incorporated by reference and the Part of the Form 10-K into which the document is
incorporated:
Portions of the Registrant’s Notice of Annual Meeting and Proxy Statement to be filed no later than 120 days following
December 31, 2020, are incorporated by reference into Part III.
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Item 1.
Item 1A.
Item 1B.
Item 2.
Item 3.
Item 4.
Item 5.
Item 6.
Item 7.
Item 7A.
Item 8.
Item 9.
Item 9A.
Item 9B.
Item 10.
Item 11.
Item 12.
Item 13.
Item 14.
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Part I
Summary of Material Risks
Business
Risk Factors
Unresolved Staff Comments
Properties
Legal Proceedings
Mine Safety Disclosures
Part II
Market for Registrant's Common Equity, Related Stockholder Matters, and Issuer Purchases of
Equity Securities
Selected Financial Data
Management's Discussion and Analysis of Financial Condition and Results of Operations
Quantitative and Qualitative Disclosures About Market Risk
Financial Statements and Supplementary Data
Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
Controls and Procedures
Other Information
Directors, Executive Officers and Corporate Governance
Part III
Executive Compensation
Security Ownership of Certain Beneficial Owners and Management and Related Stockholder
Matters
Certain Relationships and Related Transactions, and Director Independence
Principal Accountant Fees and Services
Item 15.
Item 16.
Exhibits and Financial Statement Schedules
Form 10-K Summary
Part IV
Page
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Summary of Material Risks
Laboratory Corporation of America® Holdings together with its subsidiaries (Labcorp® or the Company) is subject to a
variety of risks and uncertainties, including risks that could have a material adverse effect on its business, consolidated financial
condition, revenues, results of operations, profitability, reputation, and cash flows. This summary should be read together with
the more detailed description of the risks that the Company deems material described under “Risk Factors” in Item 1A of this
Annual Report on Form 10-K (Annual Report) and should not be relied upon as an exhaustive summary of the material risks
facing the Company’s business. In addition to the following summary, investors should carefully consider all of the information
set forth in this Annual Report, before deciding to invest in any of the Company’s securities. The risks below are not the only
ones that the Company faces. Additional risks not presently known to the Company, or that it presently deems immaterial, may
also negatively impact the Company. This Annual Report also includes forward-looking statements, immediately following this
risk summary, that involve risks or uncertainties. The Company’s results could differ materially from those anticipated in these
forward-looking statements as a result of certain factors, including the risks described below and elsewhere.
Risks Related to the COVID-19 Pandemic
a.
b.
c.
d.
The effects of the COVID-19 pandemic could have material adverse impacts on the Company’s business, results of
operations, cash flows, and financial position.
If the Company does not respond appropriately to the ongoing COVID-19 pandemic, or if the Company’s customers
do not perceive its response to be adequate, the Company could suffer damage to its reputation, which could adversely
affect its business.
The success of the Company is dependent in part on the efforts of its management team and employees, and the
COVID-19 pandemic could divert or hinder the Company’s human capital resources.
The ongoing COVID-19 pandemic has created significant volatility, uncertainty, and economic disruption that could
have an adverse effect on the Company’s financial position.
Risks Related to Regulatory and Compliance Matters
a.
b.
c.
d.
e.
f.
g.
h.
i.
Changes in payer regulations or policies, insurance regulations or approvals, or changes in or interpretations of, other
laws, regulations or policies in the U.S. or globally may have a material adverse effect upon the Company.
The Company could face significant monetary damages and penalties and/or exclusion from government programs if it
violates anti-fraud and abuse laws.
The Company’s business could be harmed from the loss or suspension of a license or imposition of fines or penalties
under, or future changes in, or interpretations of, the law or regulations of the Clinical Laboratory Improvement Act of
1967, and the Clinical Laboratory Improvement Amendments of 1988 (CLIA), or those of Medicare, Medicaid or
other national, state, or local agencies in the U.S. and other countries where the Company operates laboratories.
Failure of the Company or its third party service providers to comply with privacy and security laws and regulations
could result in fines, penalties, and damage to the Company’s reputation with customers and have a material adverse
effect upon the Company’s business.
The Company’s international operations could subject it to additional risks and expenses that could have a material
adverse impact on the business or results of operations, including exposure to liabilities under tax, trade, anti-
corruption, and data privacy laws.
Failure to comply with the regulations of drug regulatory agencies could result in fines, penalties, and sanctions and
have a material adverse effect upon the Company.
Failure to conduct animal research in compliance with animal welfare laws and regulations could result in fines,
penalties, and sanctions and have a material adverse effect upon the Company.
U.S. Food and Drug Administration (FDA) regulation of diagnostic products and increased FDA regulation of
laboratory-developed tests (LDTs) could result in increased costs, fines, and penalties.
Failure to comply with U.S., state, local or international environmental, health and safety laws and regulations,
including the U.S. Occupational Safety and Health Administration Act, and the U.S. Needlestick Safety and
Prevention Act, could result in fines and penalties.
Risks Related to the Company’s Business
a.
b.
c.
General or macro-economic factors in the U.S. and globally may have a material adverse effect upon the Company,
and a significant deterioration in the economy could negatively impact testing volumes, drug development services,
cash collections, and the availability of credit.
Healthcare reform and changes to related products, changes in government payment and reimbursement systems, or
changes in payer mix, including an increase in capitated reimbursement mechanisms and evolving delivery models,
could have a material adverse effect on the Company's revenues, profitability, and cash flow.
Changes in government regulation or in practices relating to the biopharmaceutical industry could decrease the need
for certain services that the Company provides.
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d.
e.
f.
g.
h.
i.
j.
k.
l.
Increased competition, including price competition, could have an adverse effect on the Company’s revenues and
profitability.
Failure to obtain and retain new customers, the loss of existing customers or material contracts, or a reduction in
services or tests ordered or specimens submitted by existing customers, or the inability to retain existing and/or create
new relationships with health systems could impact the Company’s ability to successfully grow its business.
Discontinuation or recalls of existing testing products, failure to develop or acquire licenses for new or improved
testing technologies, and competition from new products and technologies could adversely affect the Company’s
business.
Operations may be disrupted and adversely impacted by the effects of adverse weather, natural disasters, geopolitical
events, public health crises, hostilities or acts of terrorism, acts of vandalism, and other catastrophic events outside of
the Company's control.
Changes or disruption in services, supplies, or transportation provided by third parties could adversely affect the
Company’s business.
A failure to identify and successfully close and integrate strategic acquisition targets could have a material adverse
effect on the Company's business objectives and its revenues and profitability.
Continued and increased consolidation of managed care organizations (MCOs), biopharmaceutical companies, health
systems, physicians, and other customers could adversely affect the Company's business.
Unproductive labor environment, union strikes, work stoppages, union or works council negotiations, or failure to
comply with labor or employment laws could adversely affect the Company's operations and have a material adverse
effect upon the Company's business.
An inability to attract and retain experienced and qualified personnel, including key management personnel, could
adversely affect the Company’s business.
m. Global economic conditions and government and regulatory changes, including, but not limited to, those arising from
the U.K.'s exit from the European Union (EU), could adversely affect the Company’s business and results of
operations.
Risks Related to Financial Matters
a.
b.
c.
d.
e.
f.
The Company bears financial risk for contracts that, including for reasons beyond the Company's control, may be
underpriced, subject to cost overruns, delayed, terminated or reduced in scope.
A significant increase in the Company’s days sales outstanding could have an adverse effect on the Company’s
business, including its cash flow, by increasing its bad debt or decreasing its cash flow.
The Company's Drug Development segment revenues depend on the biopharmaceutical industry, including
biopharmaceutical companies' R&D spending, ability to raise capital, reimbursement from governmental programs or
commercial payers, and biopharmaceutical industry trends and other economic conditions.
Foreign currency exchange fluctuations could have a material adverse effect on the Company’s business.
The Company’s uses of financial instruments to limit its exposure to interest rate and currency fluctuations could
expose it to risks and financial losses that may adversely affect the Company’s financial condition, liquidity, and
results of operations.
The Company’s level of indebtedness could adversely affect the Company’s liquidity, results of operations and
business.
Risks Related to Technology and Cybersecurity
a.
b.
c.
Failure to maintain the security of information relating to the Company, or its customers, patients, or vendors, whether
as a result of cybersecurity attacks on the Company’s information systems or otherwise, could damage the Company’s
reputation, cause it to incur substantial additional costs, result in litigation and enforcement actions, and materially
adversely affect the Company’s business and operating results.
Failure or delays in the Company’s information technology systems, including the failure to develop and implement
updates and enhancements to those systems, could disrupt the Company’s operations or customer relationships.
The Company depends on third parties to provide services critical to the Company's business, and depends on them to
comply with applicable laws and regulations. Breaches of the information technology systems of third parties could
have a material adverse effect on the Company's operations.
Risks Related to Legal Matters
a.
b.
c.
d.
Adverse results in material litigation matters could have a material adverse effect upon the Company’s business.
The failure to successfully obtain, maintain and enforce intellectual property rights and defend against challenges to
the Company’s intellectual property rights could adversely affect the Company.
Changes in tax laws and regulations or the interpretation of such may have a significant impact on the financial
position, results of operations and cash flows of the Company.
If the Company fails to perform contract research services in accordance with contractual requirements and regulatory
standards, the Company could be subject to significant costs or liability.
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FORWARD-LOOKING STATEMENTS
In this Annual Report, the Company makes, and from time to time may otherwise make in its public filings, press releases
and discussions by Company management, forward-looking statements concerning the Company’s operations, performance and
financial condition, as well as its strategic objectives. Some of these forward-looking statements relate to future events and
expectations and can be identified by the use of forward-looking words such as “believes”, “expects”, “may”, “will”, “should”,
“seeks”, “approximately”, “intends”, “plans”, “estimates”, or “anticipates” or the negative of those words or other comparable
terminology. Such forward-looking statements speak only as of the time they are made and are subject to various risks and
uncertainties and the Company claims the protection afforded by the safe harbor for forward-looking statements contained in
the Private Securities Litigation Reform Act of 1995. Actual results could differ materially from those currently anticipated due
to a number of factors in addition to those discussed elsewhere herein, including in the “Summary of Material Risks” above and
in the “Risk Factors” section of this Annual Report, and in the Company’s other public filings, press releases, and discussions
with Company management, including:
1.
changes in government and third-party payer regulations, reimbursement, or coverage policies or other future reforms
in the U.S. healthcare system (or in the interpretation of current regulations), new insurance or payment systems,
including state, regional or private insurance cooperatives (e.g., health insurance exchanges) affecting governmental
and third-party coverage or reimbursement for commercial laboratory testing, including the impact of the U.S.
Protecting Access to Medicare Act of 2014 (PAMA);
2. significant monetary damages, fines, penalties, assessments, refunds, repayments, damage to the Company's reputation,
unanticipated compliance expenditures, and/or exclusion or debarment from or ineligibility to participate in
government programs, among other adverse consequences, arising from enforcement of anti-fraud and abuse laws and
other laws applicable to the Company in jurisdictions in which the Company conducts business;
3. significant fines, penalties, costs, unanticipated compliance expenditures, and/or damage to the Company’s reputation
arising from the failure to comply with applicable privacy and security laws and regulations, including the U.S. Health
Insurance Portability and Accountability Act of 1996, the U.S. Health Information Technology for Economic and
Clinical Health Act, the European Union's General Data Protection Regulation and similar laws and regulations in
jurisdictions in which the Company conducts business;
4.
loss or suspension of a license or imposition of fines or penalties under, or future changes in, or interpretations of
applicable licensing laws or regulations regarding the operation of clinical laboratories and the delivery of clinical
laboratory test results, including, but not limited to, CLIA and similar laws and regulations in jurisdictions in which the
Company conducts business;
5.
penalties or loss of license arising from the failure to comply with applicable occupational and workplace safety laws
and regulations, including the U.S. Occupational Safety and Health Administration requirements, the U.S. Needlestick
Safety and Prevention Act, and similar laws and regulations in jurisdictions in which the Company conducts business;
6.
7.
8.
9.
fines, unanticipated compliance expenditures, suspension of manufacturing, enforcement actions, damage to the
Company's reputation, injunctions, or criminal prosecution arising from failure to maintain compliance with current
good manufacturing practice regulations and similar requirements of various regulatory agencies in jurisdictions in
which the Company conducts business;
sanctions or other remedies, including fines, unanticipated compliance expenditures, enforcement actions, injunctions
or criminal prosecution arising from failure to comply with the Animal Welfare Act or applicable national, state and
local laws and regulations in jurisdictions in which the Company conducts business;
changes in testing guidelines or recommendations by government agencies, medical specialty societies, and other
authoritative bodies affecting the utilization of laboratory tests;
changes in applicable government regulations or policies affecting the approval, availability of, and the selling and
marketing of diagnostic tests, drug development, or the conduct of drug development and medical device and
diagnostic studies and trials, including regulations and policies of the U.S. Food and Drug Administration, the U.S.
Department of Agriculture, the Medicine and Healthcare products Regulatory Agency in the United Kingdom (U.K.),
the National Medical Products Administration in China, the Pharmaceutical and Medical Devices Agency in Japan, the
European Medicines Agency and similar regulations and policies of agencies in other jurisdictions in which the
Company conducts business;
10.
changes in government regulations or reimbursement pertaining to the biopharmaceutical and medical device and
diagnostic industries, changes in reimbursement of biopharmaceutical products, or reduced spending on research and
development by biopharmaceutical and medical device and diagnostic customers;
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11.
liabilities that result from the failure to comply with corporate governance requirements;
12. increased competition, including price competition, potential reduction in rates in response to price transparency and
consumerism, competitive bidding and/or changes or reductions to fee schedules, and competition from companies that
do not comply with existing laws or regulations or otherwise disregard compliance standards in the industry;
13.
changes in payer mix or payment structure, including insurance carrier participation in health insurance exchanges, an
increase in capitated reimbursement mechanisms, the impact of a shift to consumer-driven health plans or plans
carrying an increased level of member cost-sharing, and adverse changes in payer reimbursement or payer coverage
policies (implemented directly or through a third-party utilization management organization) related to specific
diagnostic tests, categories of testing or testing methodologies;
14. failure to retain or attract MCO business as a result of changes in business models, including risk based or network
approaches, out-sourced laboratory network management or utilization management companies, or other changes in
strategy or business models by MCOs;
15.
failure to obtain and retain new customers, an unfavorable change in the mix of testing services ordered, or a reduction
in tests ordered, specimens submitted, or services requested by existing customers, and delays in payments from
customers;
16.
difficulty in maintaining relationships with customers or retaining key employees as a result of uncertainty surrounding
the integration of acquisitions and the resulting negative effects on the business of the Company;
17.
18.
consolidation and convergence of MCOs, biopharmaceutical companies, health systems, large physician organizations
and other customers, potentially causing material shifts in insourcing, utilization, pricing and reimbursement, including
full and partial risk-based models;
failure to effectively develop and deploy new systems, system modifications or enhancements required in response to
evolving market and business needs;
19.
customers choosing to insource services that are or could be purchased from the Company;
20.
failure to identify, successfully close and effectively integrate and/or manage acquisitions of new businesses;
21.
22.
23.
24.
inability to achieve the expected benefits and synergies of newly-acquired businesses, including due to items not
discovered in the due diligence process, and the impact on the Company's cash position, levels of indebtedness and
stock price;
termination, loss, delay, reduction in scope or increased costs of contracts, including large contracts and multiple
contracts;
liability arising from errors or omissions in the performance of testing services, contract research services or other
contractual arrangements;
changes or disruption in the provision or transportation of services or supplies provided by third parties; or their
termination for failure to follow the Company's performance standards and requirements;
25.
damage or disruption to the Company's facilities;
26.
damage to the Company's reputation, loss of business, or other harm from acts of animal rights activists or potential
harm and/or liability arising from animal research activities;
27.
28.
29.
adverse results in litigation matters;
inability to attract and retain experienced and qualified personnel or the loss of significant personnel as a result of
illness or otherwise;
failure to develop or acquire licenses for new or improved technologies, such as point-of-care testing, mobile health
technologies, and digital pathology, or potential use of new technologies by customers and/or consumers to perform
their own tests;
30.
substantial costs arising from the inability to commercialize newly licensed tests or technologies or to obtain
appropriate coverage or reimbursement for such tests;
31.
32.
failure to obtain, maintain, and enforce intellectual property rights for protection of the Company's products and
services and defend against challenges to those rights;
scope, validity, and enforceability of patents and other proprietary rights held by third parties that may impact the
Company's ability to develop, perform, or market the Company's products or services or operate its business;
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33.
34.
35.
36.
37.
38.
39.
40.
41.
business interruption, receivable impairment, delays in cash collection impacting days sales outstanding, supply chain
disruptions, increases in operating costs, or other impacts on the business due to natural disasters, including adverse
weather, fires and earthquakes, political crises, including terrorism and war, public health crises and disease epidemics
and pandemics, and other events outside of the Company's control;
discontinuation or recalls of existing testing products;
a failure in the Company's information technology systems, including with respect to testing turnaround time and
billing processes, or the failure of the Company or its third-party suppliers and vendors to maintain the security of
business information or systems or to protect against cybersecurity attacks such as denial of service attacks, malware,
ransomware, and computer viruses, or delays or failures in the development and implementation of the Company’s
automation platforms, any of which could result in a negative effect on the Company’s performance of services, a loss
of business or increased costs, damages to the Company’s reputation, significant litigation exposure, an inability to
meet required financial reporting deadlines, or the failure to meet future regulatory or customer information
technology, data security and connectivity requirements;
business interruption, increased costs, and other adverse effects on the Company's operations due to the unionization of
employees, union strikes, work stoppages, general labor unrest or failure to comply with labor or employment laws;
failure to maintain the Company's days sales outstanding levels, cash collections (in light of increasing levels of patient
responsibility), profitability and/or reimbursement arising from unfavorable changes in third-party payer policies,
payment delays introduced by third party utilization management organizations, and increasing levels of patient
payment responsibility;
impact on the Company's revenues, cash collections, and the availability of credit for general liquidity or other
financing needs arising from a significant deterioration in the economy or financial markets or in the Company's credit
ratings by Standard & Poor's and/or Moody's;
failure to maintain the expected capital structure for the Company, including failure to maintain the Company's
investment grade rating, or leverage ratio covenants under its term loan facility and revolving credit facility;
changes in reimbursement by foreign governments and foreign currency fluctuations;
inability to obtain certain billing information from physicians, resulting in increased costs and complexity, a temporary
disruption in receipts, and ongoing reductions in reimbursements and revenues;
42. expenses and risks associated with international operations, including, but not limited to, compliance with the U.S.
Foreign Corrupt Practices Act, the U.K. Bribery Act, other applicable anti-corruption laws and regulations, trade
sanction laws and regulations, and economic, political, legal and other operational risks associated with foreign
jurisdictions;
43.
44.
45.
46.
failure to achieve expected efficiencies and savings in connection with the Company's business process improvement
initiatives;
changes in tax laws and regulations or changes in their interpretation, including the U.S. Tax Cuts and Jobs Act;
global economic conditions and government and regulatory changes, including, but not limited to those arising from
the U.K.'s exit from the European Union; and
effects, duration, and severity of the ongoing COVID-19 pandemic, including the impact on operations, personnel,
liquidity, and collections, and the actions the Company, or governments, have taken or may take in response, and
damage to the Company's reputation or loss of business resulting from the perception of the Company's response to the
COVID-19 pandemic, including the availability and accuracy and timeliness of delivery of any tests that the Company
develops, collaborates on, or provides for the detection of COVID-19, and the availability and timeliness of its drug
development services.
Except as may be required by applicable law, the Company undertakes no obligation to publicly update or revise any
forward-looking statements, whether as a result of new information, future events or otherwise. Given these uncertainties, any
forward-looking statements should not be unduly relied upon.
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Item 1.
BUSINESS
PART I
Labcorp® is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical
companies, researchers, and patients make clear and confident decisions. By leveraging its strong diagnostics and drug
development capabilities, the Company provides insights and accelerates innovations to improve health and improve lives. With
over 72,400 employees, the Company serves clients in more than 100 countries.
Through its Labcorp Diagnostics (Dx) and Labcorp Drug Development (DD) segments, the Company provides diagnostic,
drug development, and technology-enabled solutions for more than 160 million patient encounters per year, or more than 3
million patients per week. The Company also supports clinical trial activity in approximately 100 countries through its industry-
leading central laboratory, preclinical, and clinical development businesses.
The breadth of the Company's offerings has resulted in revenue growth of 23%, and operating income growth of 84%, from
2018 through 2020. The Company believes that its diversified service offerings across drug development and diagnostics also
help to balance the impact of changes in the global economic and healthcare systems, and the influence of unplanned events
such as the COVID-19 pandemic.
For the period ended December 31, 2020, the Company generated revenues of $13,978.5 million, diluted earnings per share
of $15.88, and had a total operating cash flow of $2,135.3 million.
The Company believes that science, technology and innovation are behind its successes and are foundational to its future.
The Company's commitment to leading with science and innovation enables it to improve the health and lives of people around
the world.
Rebranding
In December 2020, the Company announced an evolution of its brand identity, to highlight the pivotal role the Company
plays in healthcare and showcase the power of the Company’s combined diagnostic and drug development offerings through
one powerful brand. As part of the rebranding, the Company introduced a new company logo and has begun associating its
business unit brands with the Labcorp name. The Company’s drug development segment, formerly referred to as Covance Drug
Development, became Covance by Labcorp for a transition period, and by mid-2021 is expected to transition to Labcorp Drug
Development. The Company's diagnostics segment, formerly referred to as LabCorp Diagnostics, is transitioning to the Labcorp
name and new logo during 2021.
Enterprise Strategy
Labcorp is positioned at the convergence of research and care delivery to enable more precise and individualized healthcare,
bringing together world-class diagnostics and drug development capabilities.
The Company believes that it can continue to expand its role in the rapidly evolving healthcare environment by advancing
the following strategic priorities:
1. Leveraging the Power of the Company’s Combined Capabilities
The combination of Dx’s and DD’s core capabilities and scientific and technological expertise uniquely enables the
Company to create compelling solutions for clients. The Company’s combined strengths allow it to help biopharmaceutical and
medical device partners design better clinical studies, execute those studies faster through enhanced patient recruitment, take
greater advantage of virtual and hybrid study options, and satisfy post-market surveillance requirements. For example, the
Company can advance companion and complementary diagnostics and other precision medicine innovations that match patients
with targeted treatments based on genomics and other individual characteristics because of its experience, resources and data in
both drug development and diagnostics. Through comprehensive integration of those capabilities, the Company has a unique
opportunity to extend its position as a market leader in the development and commercialization of new therapies and tests, by
providing data, insights, and answers for doctors, drug developers, and the public.
2. Advancing the Company's Leadership Position in Oncology
Oncology continues to receive significant investment in research and treatment, but despite decades of focus and research, it
is still an area of great unmet medical need. The Company believes the diagnosis and treatment of cancer is expected to be the
fastest-growing therapeutic area for the near future.
As oncology's standard of care trends towards the adoption of precision medicine, providers are relying on advanced testing
to identify patients who will benefit from new, targeted treatments that are more effective, and usually have fewer side effects,
than traditional treatments like chemotherapy. The Company is expanding its leadership through strategic partnerships in
oncology testing, major customer wins in late-stage clinical trials, and the recruitment of leaders in the field to further build the
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Company's oncology team. In addition, the Company’s strong connections with patients, physicians, and health systems, along
with its extensive data, are powerful tools to support the Company's leadership role in diagnosing and treating cancer and its
goal of improving patient outcomes.
3. Integrating Artificial Intelligence, Data, Digitalization and Analytics Across the Company's Business
Advances in technology have impacted nearly every business, and healthcare more than most. By maximizing the use of
technology, and in particular advances in artificial intelligence, data, digitalization, and analytics, the Company strives to
improve operating efficiency and create new, differentiated products and services that the Company believes will help its
customers and will deliver better care to patients.
Artificial intelligence helps the Company to better predict trends, such as where and when demand for certain tests is likely
to change, which supports more efficient use of supplies, staffing adjustments, and the Company’s advanced logistics to route
testing to the most appropriate laboratories to deliver results quickly. Artificial intelligence capabilities and advanced logistics
have played an important role in the Company’s response to the demand for COVID-19 polymerase chain reaction (PCR)
testing.
The Company creates, and has access to, significant volumes of data. By applying advanced analytics, the Company can
help its customers improve their processes and reach better outcomes. The Company’s repository of test results help study
sponsors assess patients' eligibility for clinical trials more quickly and accurately, enroll those patients faster, shorten the time
needed for regulatory submission, and accelerate the availability of new medicines.
Digitalization is affecting every aspect of the Company’s business. For example, healthcare providers now have multiple
ways to retrieve and analyze their patients' health data; MCOs have various tools to manage their membership; consumers can
more readily access testing and their results to have more control over their care; and decentralized clinical trials can help
remove barriers that have slowed or prevented studies from being conducted in the past. As the Company experienced in 2020,
digitalization also allowed many of the Company’s employees to quickly shift from working in traditional offices to working
remotely in response to COVID-19.
4. Putting Customers at the Center of All the Company Does
Labcorp serves a broad range of customers, including MCOs, biopharmaceutical, medical device and diagnostics companies,
governmental agencies, physicians and other healthcare providers, hospitals and health systems, employers, patients and
consumers, contract research organizations (CROs), and independent clinical laboratories. The Company prioritizes a
consistent, coordinated focus across all aspects of the Company's operations, placing the customer at the center of its services,
with the objective of becoming the customer's primary partner for solutions to their needs. Customer feedback, communication
of best-practices and lessons learned, and robust employee training with respect to the needs of its customers are all methods
that the Company employs to provide a top customer experience.
The introduction of the Company’s new branding is intended to send a clear signal of who the Company is, what it does, and
how it is differentiated from its competitors. It is the Company's goal that the Labcorp brand represents a promise to its
customers about how they will be treated, and the levels of service, quality, and innovation that the Company will deliver.
5. Evaluate and Execute on High-Growth Opportunities
The Company has a long history of disciplined use of capital to invest in the growth of the business. The Company has made
significant investments in the deployment of new technologies through both licensing and internal research and development,
strategic and fold-in acquisitions, and establishing collaborative partnerships with other leading companies and organizations
that share the Company’s goals and expectations.
The Company continually evaluates its business and the broader healthcare and life sciences markets to proactively identify
and assess:
•
•
•
•
•
potential growth opportunities;
business areas that might not support continued growth and should be revamped or divested;
acquisition targets that meet its criteria for quality, value, and return on investment;
new products that would successfully integrate with or extend the Company’s offerings; and
a balanced formula for capital allocation.
Through continued focus on these priorities, the Company expects to be in the optimal position to make tough, disciplined
choices that maximize shareholder value, better protect the Company from market fluctuations and outside impacts, and fuel
significant, profitable revenue growth.
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COVID-19 Response
The Company has been intensely focused on supporting the fight against COVID-19 since the earliest stages of the
pandemic.
Diagnostic Testing and Clinical Trial Leadership
In tandem with the first confirmed cases, the Company began preparations to be able to offer diagnostic testing to identify
cases of COVID-19, working closely with diagnostic manufacturers and suppliers, and with regulators and public health
authorities.
On March 5, 2020, the Company became the first commercial laboratory in the U.S. to launch PCR testing for COVID-19,
and the Company received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) on
March 16, 2020. That was the first of a steady series of innovations introduced by the Company to rapidly expand COVID-19
test capacity, options, access, and efficiency. These COVID-19 innovations include:
•
•
•
•
•
the first FDA EUA for an at-home collection kit on its Pixel by Labcorp® platform;
the first digital COVID-19 service, which is also available through healthcare providers from the Company’s Labcorp at
Home offering;
early participation in COVID-19 research projects in collaboration with partners that included Adaptive Biotechnologies,
Microsoft, and Pacific Biosciences;
introduction of new test options to increase test capacity, throughput, and efficiency to maximize use of supplies, including
the introduction of a new method to extract RNA from samples using heat and technology; and
the increased use of robotics and automation in the PCR testing process.
The Company has steadily increased its COVID-19 test capacity, from several thousand PCR tests per day in early March to
275,000 per day by the end of 2020. The Company performed over 31 million PCR tests and nearly 4 million antibody tests in
2020.
As a result, the Company developed an expertise and understanding of COVID-19 that led to it becoming a leader in
supporting clinical trials of potential treatments and vaccines for the virus. By the end of 2020, the Company had won
approximately 440 COVID-19 trial and study opportunities, from small nonclinical programs to late-stage clinical trials.
Base Business Normalization
In the initial months of the COVID-19 pandemic, the Company experienced a significant drop in its non-COVID-19
business (Base Business) as patients avoided routine medical care and most elective and non-emergency procedures were
postponed. This decline, coupled with the suspension of most global clinical trial activity resulted in a negative impact to the
Company's Base Business in the latter part of the first quarter and initial part of the second quarter of 2020. By the end of the
second quarter of 2020, however, the Company experienced a steady recovery in its Base Business, which continued through
the third quarter of 2020. During the fourth quarter, the Dx Base Business volume recovery flattened with volumes below prior
year in the high single digits. Throughout 2020, the Company's PCR and antibody COVID-19 testing (COVID-19 Testing) has
helped to more than offset the pressure experienced in the Base Business.
COVID-19 Outlook
COVID-19 has had, and continues to have, an extensive impact on the global health and economic environments. The
Company is closely monitoring the impact of the COVID-19 pandemic on all aspects of the business, given the continued
unpredictability and the corresponding government restrictions and customer behavior.
While the Company anticipates that COVID-19 will continue to have a significant impact on its business through 2021 and
potentially beyond, the Company expects that the rollout of COVID-19 vaccines will likely lead to a gradual decline in the
demand for COVID-19 Testing. As a result, COVID-19 Testing demand is not predicted to match 2020 levels. However, the
Company believes that other diagnostic testing should continue to expand, and both COVID-19 and non-COVID-19 drug
development activity is expected to grow in 2021.
Capital Allocation
The Company believes it has a strong track record of deploying capital to investments that enhance the Company's business
and return capital to shareholders.
During 2020, the Company invested $267.6 million in strategic business acquisitions. The acquisitions have expanded the
Company’s service offerings, expanded its customer and revenue mix, and strengthened and broadened the scope of its
geographic presence. The Company continues to evaluate acquisition opportunities that leverage the Company’s core
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competencies, complement existing scientific and technological capabilities, increase the Company’s presence in key
geographic, therapeutic and strategic areas, and meet or exceed the Company’s financial criteria.
During 2020, the Company purchased 0.6 million shares of its common stock at an average price of $178.85 for a total cost
of $100.0 million. After making these purchases in the first quarter, the Company temporarily suspended its share repurchase
program as a part of the fiscal measures it took in response to the uncertainty of the COVID-19 pandemic, to preserve liquidity
and financial flexibility. The Company reinstated its share repurchase program in the fourth quarter but made no additional
purchases in 2020. At the end of 2020, the Company had a remaining authorization with no expiration date to purchase an
additional $800.0 million of Company common stock.
During 2020, capital expenditures were $381.7 million and the Company also repaid $412.2 million of its Senior Notes. The
Company expects capital expenditures in 2021 to be approximately 4.0% of revenues, primarily in connection with projects to
support growth in the Company's core businesses, facility expansion and updates, projects related to both ongoing and new
LaunchPad initiatives, and further acquisition integration initiatives.
The Company will continue to evaluate all opportunities for strategic deployment of capital in light of market conditions.
Seasonality and External Factors
The Company experiences seasonality across its business. For example, testing volume generally declines during the year-
end holiday period and other major holidays and can also decline due to inclement weather or natural disasters. Declines in
testing volume reduce revenues, operating margins and cash flows. Operations are also impacted by changes in the global
economy, exchange rate fluctuations, political and regulatory changes, the progress of ongoing studies and the startup of new
studies, as well as the level of expenditures made by the biopharmaceutical industry in R&D. In 2020, as discussed in more
detail elsewhere in Item 1, COVID-19 had significant impact on the Company. This impact included both the effect of the
Company’s response to the virus through its testing and drug development services and the effect of COVID-19 on the global
economy and how that affected demand for the Company’s non-COVID-19 services.
In 2020, approximately 10.7% of the Company's revenues were billed in currencies other than the U.S. dollar, with the
Swiss franc, British pound, Canadian dollar, and the euro representing the largest components of its currency exposure. Given
the seasonality and changing economic factors impacting the business, comparison of the results for successive quarters may
not accurately reflect trends or results for the full year.
Company Reporting
The Company’s Annual Report on Form 10-K, Quarterly Reports on Form 10-Q, Current Reports on Form 8-K, and all
amendments to those reports are made available free of charge through the Investor Relations section of the Company’s website
at www.labcorp.com as soon as reasonably practicable after such material is electronically filed with, or furnished to, the U.S.
Securities and Exchange Commission (SEC). Additionally, the SEC maintains a website at http://www.sec.gov that contains
reports, proxy and information statements, and other information regarding issuers, including the Company, that file
electronically with the SEC.
The matters discussed in this “Business” section should be read in conjunction with the Consolidated Financial Statements
found in Item 8 of Part II of this Annual Report, which include additional financial information about the Company. This
Annual Report includes forward-looking statements that involve risks or uncertainties. The Company’s results could differ
materially from those anticipated in these forward-looking statements as a result of certain factors, including the risk factors
described in Item 1A of Part I of this Annual Report and elsewhere. For more information about forward-looking statements,
see “Forward-Looking Statements” included prior to Part I in this Annual Report.
The Company's Business
The Company experienced growth across all key financial metrics in 2020.
Revenues
Gross profit
Operating income
Net earnings attributable to Laboratory Corporation of America Holdings
Cash flows from operating activities
Basic earnings per common share
Diluted earnings per common share
12
Years Ended December 31,
2020
13,978.5 $
4,952.8 $
2,445.4 $
1,556.1 $
2,135.3 $
15.99 $
15.88 $
2019
11,554.8
3,252.5
1,330.2
823.8
1,444.7
8.42
8.35
$
$
$
$
$
$
$
Index
The Company reports its business in two segments, Dx and DD. In 2020, Dx and DD contributed 65% and 35%,
respectively, of revenues to the Company, and in 2019 contributed 60% and 40%, respectively. Nearly all of Dx’s revenues are
generated in the U.S., with a smaller portion in Canada and a relatively small amount in the rest of the world. DD’s revenues
are nearly evenly split between the U.S. and the rest of the world, with approximately 49% derived from the U.S. and
approximately 51% from other countries. Although this allocation of revenues provides some protection from economic shifts
in any one country, it is still heavily tilted towards the U.S. As a result, the Company continues to actively explore new and
expanded business opportunities outside the U.S. to further diversify its sources of revenues. The Company's revenues by
segment payers/customer groups and by geography for the years ended December 31, 2020, 2019 and 2018 are as follows:
For the Year Ended
December 31, 2020
For the Year Ended
December 31, 2019
For the Year Ended
December 31, 2018
North
North
North
America Europe Other
Total
America Europe Other
Total
America Europe Other
Total
Payer/Customer
Dx
Clients
Patients
Medicare and Medicaid
Third-party
Total Dx revenues by payer
DD
Biopharmaceutical and
medical device companies
20 %
6 %
7 %
32 %
65 %
— %
— %
— %
— %
— %
— %
— %
— %
— %
— %
20 %
6 %
7 %
32 %
65 %
17 %
8 %
8 %
27 %
60 %
— %
— %
— %
— %
— %
— %
— %
— %
— %
— %
17 %
8 %
8 %
27 %
60 %
18 % — % — % 18 %
8 % — % — %
8 %
9 %
9 % — % — %
27 % — % — % 27 %
62 % — % — % 62 %
17 %
11 %
7 %
35 %
21 %
12 %
7 %
40 %
19 % 12 %
7 % 38 %
Total revenues
82 %
11 %
7 % 100 %
81 %
12 %
7 % 100 %
81 % 12 %
7 % 100 %
During 2020, the Dx segment generated $9,253.4 million in total revenues and $2,634.9 million in operating income,
resulting in an operating margin of 28.5%.
Dx Segment
Dollars in millions
Revenues
Operating income
Year Ended December 31,
2020
2019
$
$
9,253.4 $
2,634.9 $
7,000.1
1,086.0
Dx is an independent clinical laboratory business. It offers a comprehensive menu of frequently requested and specialty
testing through an integrated network of primary and specialty laboratories across the U.S. This network is supported by a
sophisticated information technology system, with more than 75,000 electronic interfaces to deliver test results, nimble and
efficient logistics, and local labs offering rapid response testing.
Dx also provides patient access points, strategically and conveniently located throughout the U.S., including nearly 2,000
patient service centers (PSCs) operated by Dx and more than 6,000 in-office phlebotomists who are located in customer offices
and facilities. Although testing for healthcare purposes and customers who provide healthcare services represents the most
significant portion of the clinical laboratory industry, clinical laboratories also perform testing for other purposes and
customers, including employment and occupational testing, DNA testing to determine parentage and to assist in immigration
eligibility determinations, environmental testing, wellness testing, toxicology testing, pain management testing, and medical
drug monitoring. Dx offers an expansive test menu including a wide range of clinical, anatomic pathology, genetic and genomic
tests, and regularly adds new tests and improves the methodology of existing tests to enhance patient care. Dx also offers
consumer-initiated wellness testing available online through its Pixel by Labcorp® platform, which saw growth and increased
consumer awareness in 2020 as a result of offering the first at-home collection kit for COVID-19 PCR testing to receive an
EUA from the FDA and the first to receive an EUA for retail availability without a prescription. The COVID-19 at-home
collection kits are also available for healthcare providers to order for their patients through Labcorp at Home.
Through the dedicated effort of approximately 42,000 employees, Dx typically processes tests for more than 3 million
patient encounters each week.
As part of an ongoing commitment to be an efficient and high value provider of laboratory services, beginning in 2015, Dx
implemented a comprehensive business process improvement initiative, referred to as LaunchPad, to reengineer its systems and
processes to create a sustainable and more efficient business model, and to improve the experience of all stakeholders. Dx
achieved its goals for the initial phase of LaunchPad of delivering both short- and long-term savings, and implementing system
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and process improvements that are expected to continue to yield benefits for the foreseeable future. Dx has subsequently
extended LaunchPad, adding new enterprise-wide projects and establishing the initiative as an ongoing continuous
improvement program. Dx’s LaunchPad initiative is currently on track to deliver approximately $200.0 million in net savings
for the period of late 2018 through the end of 2021, while incurring approximately $40.0 million in one-time implementation
costs.
The Dx business can be categorized into the following components:
Service
Key Features
Testing Operations and
Productivity
Testing and Related
Services
Development of New
Tests
• Network of PSCs offering specimen selection services
• Comprehensive, nimble supply chain for transferring specimens across the entire life cycle of a
patient sample
• 1-2 day turnaround time for most test results, with the vast majority of results delivered
electronically to healthcare providers
• Rigorous standard of quality - 27 regional/specialty labs hold ISO 15189 certification
• Standard Testing Services - frequently-ordered tests used in regular patient care include blood
chemistry analyses, urinalyses, blood cell counts, thyroid tests, PAP tests, hemoglobin A1C,
prostate-specific antigen (PSA), tests for sexually transmitted diseases (e.g. chlamydia,
gonorrhea, trichomoniasis and human immunodeficiency (HIV), and hepatitis C (HCV)),
vitamin D, microbiology cultures and procedures, and alcohol and other substance-abuse tests
• Specialty Testing Services - industry leader in gene-based and esoteric testing; advanced tests
target specific diseases and use new technologies including anatomic pathology/oncology,
cardiovascular disease, coagulation, diagnostic genetics, endocrinology, infectious disease,
women's health, pharmacogenetics, parentage and donor testing, occupational testing services,
medical drug monitoring services, chronic disease programs, and kidney stone prevention
• Dx offers a range of health and wellness services to employers and MCOs, including health
fairs, on-site and at-home testing, vaccinations and health screenings
• Approximately 100 new tests launched in 2020
• Active diagnostics and therpeutics research division: Nearly 700 studies, articles, and
presentations produced in 2020
• Continuous investing, internally and externally, in new testing technologies and advanced
testing capabilities
A range of services and support using proprietary technologies to improve the customer and patient
experience and provide convenient access to data and analytics, including:
• More than 6 million enhanced clinical decision support (CDS) reports delivered to physicians
and health systems
Development of New
Tests
• Online and mobile applications allowing patients to check test results, schedule appointments
and manage their accounts
• Patient self-service apps for scheduling PSC visits, checking in upon arrival, and completing
documentation, expediting and improving the patient experience
• Online applications for MCOs and accountable care organizations (ACOs) to obtain test results
and quality data
Effect of U.S. Market Changes on the Clinical Laboratory Business
The delivery of, and reimbursement for, healthcare continues to change in the U.S., impacting all stakeholders, including
the clinical laboratory business. Medicare (which principally serves patients who are 65 and older), Medicaid (which principally
serves low-income patients) and insurers have increased their efforts to control the cost, utilization and delivery of healthcare
services. Measures to regulate healthcare delivery in general and clinical laboratories in particular have resulted in reduced
prices, added costs and decreased test utilization for the clinical laboratory industry by imposing new, increasingly complex
regulatory and administrative requirements. The government also has continued to adjust the Medicare and Medicaid fee
schedules at the national and local level, and Dx believes that pressure to reduce government reimbursement will continue.
Fees for most laboratory services reimbursed by Medicare are established in the Clinical Laboratory Fee Schedule (CLFS)
and fees for other testing reimbursed by Medicare, primarily related to pathology, are covered by the Physician Fee Schedule
(PFS). During 2020, approximately 8.8% of Dx’s revenue was reimbursed under the CLFS (11.7% in 2019), and approximately
0.4% was reimbursed under the PFS (0.6% in 2019). Over the past several years, Dx has experienced governmental
reimbursement reductions as a direct result of several Congressional acts and regulatory initiatives, the most significant of
which was PAMA. PAMA, which became law on April 1, 2014, and which went into effect on January 1, 2018, resulted in a
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net reduction in reimbursement revenue of approximately $72.0 million in 2020 from all payers affected by the CLFS
(approximately $107.0 million in 2019). These laws include provisions designed to control healthcare expenses reimbursed by
government programs through a combination of reductions to fee schedules, incentives to physicians to participate in alternative
payment models such as risk-sharing, and new methods to establish and adjust fees.
In 2020, Dx realized a net reduction of approximately $0.5 million in PFS revenue, driven by reductions in reimbursement
for flow cytometry procedures ($1.9 million in 2019). In 2020, Dx realized an increase of approximately $10.1 million in
aggregate Medicare reimbursement associated with the suspension of sequestration through December of 2020 as a result of
provisions included in the CARES Act. In 2021, Dx anticipates it will realize increases of approximately $0.3 million in PFS
revenue and $4.1 million in aggregate Medicare reimbursement associated with the extended suspension of sequestration
through March 2021 as a result of provisions included in the Omnibus Appropriations and Coronavirus Relief Package.
Beginning in 2018, under PAMA, the Centers for Medicare and Medicaid Services (CMS) of the U.S. Department of
Health and Human Services (HHS) set the CLFS using the weighted median of reported private payer prices paid to certain
laboratories that receive a majority of their Medicare revenue from the CLFS and PFS and that bill Medicare under their own
National Provider Identifier (NPI). Applicable labs, including Dx, were required to begin reporting their test-specific private
payer payment amounts to CMS during the first quarter of 2017. CMS used that private market data to calculate weighted
median prices for each test (based on applicable current procedural technology (CPT) codes) to represent the new CLFS rates
beginning in 2018, subject to certain phase-in limits. For 2018-2020, a test price could not be reduced by more than 10.0% per
year. As a result of provisions included within the CARES Act, passed by Congress in 2020, PAMA rate reductions for 2021
have been suspended, and therefore the Company will not experience any incremental reimbursement rate impact due to PAMA
in 2021.
For 2022-2024, a test price cannot be reduced by more than 15.0% per year. The process of data reporting and repricing
will be repeated every three years for Clinical Diagnostic Laboratory Tests (CDLTs) beginning in 2022. Under current law, as
revised in the CARES Act, the next data reporting period for CDLTs (based on data collected in 2019) will occur during the
first quarter of 2022, and new CLFS rates for CDLTs will be established based on that data beginning in 2023, subject to the
previously described phase-in limits. The subsequent data reporting period for CDLTs (based on data collected in 2023) will
occur during the first quarter of 2025, and new CLFS rates for CDLTs will be established based on that data beginning in
2026. CLFS rates for 2025 and subsequent periods will not be subject to phase-in limits. CLFS rates for Advanced Diagnostic
Laboratory Tests will be updated annually.
The American Clinical Laboratory Association (ACLA) has filed a federal civil action challenging the legal basis for the
data collection methodology CMS used to derive the data from which the median prices were calculated. Since the initial data
collection, CMS has revised its PAMA regulations to increase the number of hospital outreach labs that will be required to
report private market data in future collections. Reports by the U.S. Government Accountability Office (GAO) and the HHS
Office of Inspector General (OIG) on PAMA implementation have identified certain instances of actual or potential increased
Medicare expenditures under PAMA that could result in further efforts to amend PAMA by Congress.
ACLA continues to work with Congress on potential legislative reform of PAMA, which if adopted could reduce the
negative impact of PAMA as currently implemented by CMS. Under the Laboratory Access for Beneficiaries (LAB) Act, the
Medicare Payment Advisory Commission is required to conduct a study and make recommendations to Congress on ways to
improve data collection, reporting, and rate setting under PAMA to achieve, in a less burdensome manner, CLFS rates that
accurately and fairly reflect private market rates. The Company supports the ongoing efforts to prevent or lessen the negative
impact of the changes to the CLFS pursuant to PAMA, and the full impact of those efforts, and what the long-term effect will
be on the CLFS rates is not yet known.
Further healthcare reform could occur in 2021, including changes to the ACA and Medicare reform, initiatives to address
surprise billing and increased price transparency, as well as administrative requirements that may continue to affect coverage,
reimbursement, and utilization of laboratory services in ways that are currently unpredictable.
In addition, market-based changes have affected and will continue to affect the clinical laboratory business. Reimbursement
from commercial payers for diagnostic testing may shift away from traditional, fee-for-service models to alternatives, including
value-based, bundled pay-for-performance, and other risk-sharing payment models. The growth of the managed care sector and
consolidation of MCOs present various challenges and opportunities to Dx and other clinical laboratories.
The Company serves many MCOs. These organizations have different contracting philosophies, which are influenced by
the design of their products. Some MCOs contract with a limited number of clinical laboratories and engage in direct
negotiation of rates. Other MCOs adopt broader networks with generally uniform fee structures for participating clinical
laboratories. In some cases, those fee structures are specific to independent clinical laboratories, while the fees paid to hospital-
based and physician-office laboratories may be different, and are typically higher. MCOs may also offer Managed Medicare or
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Managed Medicaid plans. In addition, some MCOs use capitation rates to fix the cost of laboratory testing services for their
enrollees. Under a capitated reimbursement arrangement, the clinical laboratory receives a per-member, per-month payment for
an agreed upon menu of laboratory tests provided to MCO members during the month, regardless of the number of tests
performed. For the year ended December 31, 2020, capitated contracts with MCOs accounted for approximately $319.0 million,
or 3.4%, of Dx's revenues. Dx's ability to attract and retain MCO customers has become even more important as the impact of
various healthcare reform initiatives continues, including expanded health insurance exchanges and ACOs.
In addition to reductions in test reimbursement, the Company also anticipates potential declines in test volumes as a result
of increased controls over the utilization of laboratory services by Medicare, Medicaid, and other third-party payers, particularly
MCOs. MCOs are implementing, directly or through third parties, various types of laboratory benefit management programs,
which may include lab networks, utilization management tools (such as prior authorization and/or prior notification), and claims
edits, which impact coverage and reimbursement of clinical laboratory tests. Some of these programs address clinical laboratory
testing broadly, while others are focused on certain types of testing, including molecular, genetic and toxicology testing. In
addition, continued movement by patients into consumer-driven health plans may have an impact on the utilization of
laboratory testing.
Despite the overall negative market changes regarding reimbursement discussed above, Dx believes that the volume of
clinical laboratory testing is positively influenced by several factors, including the expansion of Medicaid, managed care, and
private insurance exchanges. In addition, Dx believes that increased knowledge of the human genome and continued innovation
in laboratory medicine will continue to foster greater appreciation of the value of gene-based diagnostic assays. Additional
factors that may lead to future volume growth include an increase in the number and types of tests that are readily available
(due to advances in technology and increased cost efficiencies) for the diagnosis of disease, and the general aging of the U.S.
population. Dx also believes that it and other large, independent clinical laboratory testing companies will be able to increase
their share of the overall clinical laboratory testing market due to a number of market factors, primarily related to a continued
drive to improve outcomes and reduce costs across the healthcare system. Dx believes that its enhanced and growing esoteric
menu of tests, leading position with companion diagnostics, broad geographic footprint, and operating efficiency provide a
strong platform for growth.
During 2020, the DD segment generated $4,877.7 million in total revenue and $37.3 million in operating income, resulting
DD Segment
in an operating margin of 0.8%.
Dollars in millions
Revenues
Operating income
Year Ended December 31,
2020
2019
$
$
4,877.7 $
37.3 $
4,578.1
411.5
DD provides end-to-end drug development, medical device and companion diagnostic development solutions from early-
stage research to clinical development and commercial market access. Its customers are comprised of biopharmaceutical,
medical device, and diagnostic companies across the world. With more than 28,000 employees worldwide and a global network
of operations, DD offers deep expertise in early development and clinical trials in each therapeutic area. DD collaborated on
87% of the novel drugs approved by the U.S. FDA in 2020, including 86% of the novel oncology drugs and 88% of the rare and
orphan disease drugs. Through its industry-leading central laboratory business it supports clinical trial activity in approximately
100 countries. In late 2018, the Company commenced a series of LaunchPad projects focused on DD, which delivered in excess
of $150.0 million of net savings through 2020.
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Service
Key Features
• Lead optimization: connects early discovery activities to regulated pre-clinical studies
• Analytical services: bioanalytical testing services offering appropriate dose and frequency of
drug administration
• Safety assessment: general, genetic, and immunotoxicology services; nonclinical pathology;
safety pharmacology services; preclinical medical device services; respiratory services; and
developmental and reproductive toxicology (DART) studies
Preclinical Services
• Chemistry manufacturing services: robust, cost-effective solutions in the areas of safety,
identity, strength, quality, and purity assessments for biologics
• Early phase development solutions: focused, multidisciplinary teams of experts that craft
integrated solutions to identify and develop lead drug candidates and reduce development
challenges
• Crop protection and chemical testing: Consulting services for chemical manufacturers and
other firms engaged in the development of modern crop protection technology
• Clinical laboratory services for individuals participating in clinical studies
• Provided to biopharmaceutical customers through its global network of central laboratories in
the U.S., Europe, and Asia
• Operates world's largest automated clinical trial sample collection kit production line that
enables kits to be produced with 5.5 sigma precision
• Seven ISO 15189-certified laboratories
• Collaborated with more than 60 clients on more than 180 companion diagnostic projects in 2020
• Comprehensive range of services including the full service delivery of Phase I through IV
clinical studies, along with a wide offering of functional service provider solutions
• Dedicated group experienced in conduct of trials for medical devices and diagnostics to provide
services for expanding market in medical devices
• Leader in clinical pharmacology
• Wide range of commercialization solutions including life cycle management and post-approval
studies
• Market access solutions
Proprietary digital tools and services providing customer with greater access to key insights and
results, as well as improved trial management, enhanced transparency, quality, and speed of clinical
trials, that results in reduced costs and increased market potential for customers:
• Patient-facing software applications supporting virtual, hybrid, and traditional trials
• Metrics and benchmarking applications for trial performance monitoring and optimization
• Award-winning informatics software suite for risk-based quality management across clinical
trials
• Patient randomization and Clinical Supply Management
Central Laboratory
Services
Clinical Development
and Commercialization
Services
Technology Solutions
Human Capital
The purpose-driven mission of the Company is “improving health and improving lives.” Given the nature of the Company's
global life sciences business, the Company's employees are critical to its success. It takes the efforts and focus of all of the
Company's specialized and highly skilled employees to deliver the power of the combined Dx and DD segments to patients and
customers throughout the world. The COVID-19 pandemic during 2020 provided unique challenges to the Company, and its
employees were paramount to the Company's ability to meet the increasing needs of patients and customers.
Workforce Demographics
The Company's future success is dependent on its continued capabilities to recruit, develop, and retain a specialized and
highly skilled global workforce, and the Company believes that it has good working relationships with its employees. The
Company's 72,400 employees are globally dispersed, with 77% in the U.S. and Canada, 10% in the Asia region, 13% in the
EMEA region, and less than 1% in the Latin American region. The Company's workforce is 61% in the Dx segment and 39% in
the DD segment, with 90% full-time, and 10% part-time. Approximately 3.6% of the Company's global workforce is employed
under a collective bargaining agreement. To manage fluctuations in volume and other business demands, the Company uses
contingent labor to supplement its workforce by approximately 10%.
Throughout the pandemic, a significant portion of the Company's employees have been working diligently to serve patients
and customers. To meet the increased demands of the pandemic, the Company increased its global workforce by 12.5% during
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2020. To promote the safety and welfare of its employees, the Company transitioned those employees who do not work with
patients, animals, in labs or logistics, to remote working.
Diversity and Inclusion
The Company has a diverse workforce with a broad range of unique experiences and talents. The Company believes that the
diversity of its employees and its inclusive programs contribute to a healthy, productive, and respectful work environment.
Workforce Diversity Profile:
United States: Gender and Ethnicity
U.S. Employees
Male
Female
White
Executive/Managerial
Professional and Sales
Technician/Admin/Operatives
Totals
40%
34%
24%
29%
60%
66%
76%
71%
70%
62%
45%
52%
Total Non
White
30%
38%
55%
48%
Black
Hispanic
Asian
Other
13%
14%
29%
23%
6 %
7%
14%
12%
9 %
14%
8%
10 %
2%
3%
4%
3%
Total U.S. headcount on payroll as of 12/31/20, excluding casual employees and event workers employed by Labcorp Staffing Solutions.
Global: Gender
Total U.S. headcount on payroll as of 12/31/20, excluding casual employees and event workers employed by Labcorp Staffing Solutions.
The social unrest and unique impact of the pandemic around the world in 2020 provided the Company an opportunity to
refocus efforts to further improve its diversity profile for the benefit of employees, patients, and customers. The Company
appointed a new Chief Diversity and Inclusion Officer (CDIO), who reports dually to the Chief Executive Officer (CEO) and
Chief Human Resources Officer (CHRO). The CDIO also provides periodic reports to the Compensation and Human Capital
Committee of the Board of Directors.
The Company’s key diversity and inclusion priorities going forward include: empowering inclusive leadership, developing
and sustaining a diverse talent pipeline, and creating an environment for engagement across the Company and in its
communities. The Company's leadership is engaging with its six employee resource groups with 50 chapters around the world,
to drive these diversity and inclusion priorities.
In 2021, the Company was recognized for the fourth consecutive year as a Best Place to Work for LGBTQ Equality with a
perfect score from Human Rights Campaign's Corporate Equality Index, the nation's premier benchmarking survey and report
on corporate policies and practices related to LGBTQ workplace equality. The Company was also named to FORTUNE®
magazine's 2021 List of World's Most Admired Companies, making the annual list for the third time, as well as the 2020 List of
World's Best Employers and as one of Forbes' 2020 List of the Best Employers for New Graduates.
Compensation and Benefits
As the Company's business becomes increasingly complex, global, mobile, and technology-enabled, it recognizes the
importance of having compensation and benefits programs that provide sufficient flexibility to attract and retain the specialized
and skilled talent needed to move the business forward. The Company continually monitors market activity and employee
movement to maintain competitiveness in a dynamic life sciences industry.
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Global Employees - GenderMale29%Female71%MaleFemaleGlobal Employees, Managers/Executives - GenderMale40%Female60%MaleFemale Index
During the pandemic, the Company has taken steps to protect our competitive positioning with a focus on front line workers,
given their on-premises direct interaction with patients and the handling of specimens and results throughout the supply chain
and operations. Although the Company initially suspended discretionary payments, such as the annual merit adjustments and
U.S. 401K company contributions, in July 2020, as business improved, the Company retroactively reinstated both programs,
returning over $100 million back to our employees globally. In addition, during 2020, the company provided over $50 million
in discretionary incentives and awards to our employees globally to thank and reward them for their response to the pandemic.
The Company also made over $8 million in broad, off-cycle wage rate adjustments, primarily to its U.S. non-exempt
employees.
The Company is focusing on enhancing our benefits positioning by not increasing employee contributions in 2021 for the
U.S. non-union medical, dental, and vision plans, as well as providing disability coverage at no cost to U.S. non-union
employees. In the area of wellness, the Company covered the cost or provided a subsidy to all global employees for flu shots to
protect their health and safety, as well as the health and safety of patients and customers. The Company built these
enhancements on top of other benefits and wellness programs, such as in the U.S. medical plans where the Company subsidizes
part of the monthly contributions for employees earning less than $50,000 annually and provides up to $1,000 in medical
reimbursements for engaging in healthy activities. The Company also provides U.S. employees a $300 fitness reimbursement to
encourage healthy lifestyles.
Development and Training
Because the life sciences industry is heavily regulated, the Dx and DD segments require a significant investment in technical
training to prepare their workforces to meet the necessary standards to run and manage business operations. Across the
enterprise considerable attention is focused on employee skills training.
While the technical training is important to the Company’s success in differentiating its science and technology, the
Company also invests in training for the professional development of its talent and to retain its best employees for future
opportunities in the Company. In 2020, 3,500 employees attended professional development webinars consisting of 7,000 hours
of professional development. To strengthen leadership capabilities, the organization provided 6,200 hours of core leadership
training to early in career leaders. Finally, the expanded mentoring program had 2,100 employees participate with 10,200
mentoring hours recorded from April to December 2020.
The pandemic has provided challenges to the ability to provide both technical and leadership training. The Company has
adapted by utilizing technology to deliver unique virtual learning and development opportunities.
Health and Safety
The nature of the Dx and DD business segments requires employees to work directly with patients, handle, process or test
human specimens on a daily basis. As a result, the health and safety of the Company's employees is a primary concern. The
Company has established procedures, processes and controls, including providing personal protective equipment (PPE) to
protect our employees. During the pandemic, the Company supplied more than 250 million units of PPE to employees,
including personal cloth facemasks for each employee, N95 respirators, and ear-loop masks, gloves, face shields and disposable
lab coats.
Employee Giving
The COVID-19 crisis left many communities and individuals facing health challenges and financial crisis. Through the
Company’s U.S. annual Employee Giving Campaign, donations helped to support the American Cancer Society, American
Heart Association, American Diabetes Association, American Red Cross Disaster Relief, United Way, and the National Urban
League. The National Urban League was added based on feedback from the Company's employees requesting a charity focused
on social and economic justice. The Company and its employees focused their efforts on helping the underserved in 2020 by
donating to local food pantries and shelters, by supporting educational programs aimed at helping to provide students and
teachers with the resources they needed during the pandemic and supporting a number of patient assistance programs aimed at
helping the underserved while they received care. In addition, the Company established the Labcorp Charitable Foundation
which supports the Company’s strategic mission of improving health and improving lives with contributions focused on health
and welfare, education and community.
Customers
The Company provides its services to a broad range of customers across Dx and DD. The primary customer groups serviced
by the Company include:
• MCOs. The Company serves many MCOs, each of which operate on a national, regional, or local basis.
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• Biopharmaceutical, Medical Device, and Diagnostics Companies. The Company provides development services to
hundreds of biopharmaceutical (including pharmaceutical and biotechnology-based organizations), medical device, and
diagnostics companies, ranging from the world's largest multi-nationals to emerging, mid-market companies.
• Physicians and Other Healthcare Providers. Physicians who require clinical laboratory testing for their patients are a
primary source of requests for Dx's testing services.
• Hospitals and Health Systems. The Company provides hospitals and health systems with services ranging from core and
specialty testing to supply chain and technical support services, and the opportunity to be a research partner for participation
in studies and clinical trials with DD. In some cases, a hospital’s on-site laboratory may be operated or managed by an
outside contractor or independent laboratory, including the Company.
• Other Customers. The Company serves a broad range of other customers, including, but not limited to, governmental
agencies, employers, patients and consumers, CROs, crop protection and chemical companies, academic institutions and
independent clinical laboratories.
Sales, Marketing, and Customer Service
The Company offers its services through a sales force focused on serving the specific needs of customers in different market
segments. The Company's sales force is responsible for both new sales and for customer retention and relationship building.
For Dx, these market segments generally include primary care, women's health, specialty medicine (e.g., infectious diseases,
endocrinology, gastroenterology, and rheumatology), oncology, ACOs, and hospitals and health systems, with different
representatives focused on each segment to better understand and respond to the unique needs of each clinical area. DD’s global
sales organization provides customer coverage across the biopharmaceutical industry for services including lead optimization,
preclinical safety assessment, analytical services, clinical trials, central laboratories, biomarkers, and companion diagnostics,
market access and technology solutions. As part of its ongoing strategic priority to maximize the power of the combined, sales
representatives from each business segment work together on outreach to potential customers of each business, including
hospitals and health systems that may purchase testing and participate in clinical trials, or biopharmaceutical companies whose
studies may benefit from use of Dx’s specialty testing or network of PSCs.
In 2020, the Company initiated a greater emphasis on establishing a centralized marketing program to support both of its
primary business segments, rather than separate programs for each segment. The Company anticipates that this will provide
further support for fully leveraging the power of its combined capabilities, and it is also aligned with the Company’s rebranding
initiative, which was launched in December 2020.
Market Opportunity
Dx
The Company believes that in 2020, the U.S. clinical laboratory testing industry generated revenues of more than $80
billion. The clinical laboratory industry consists primarily of three types of providers: hospital-based laboratories, physician-
office laboratories and independent clinical and anatomical pathology laboratories, such as those operated by Dx.
The clinical laboratory business is intensely competitive. CMS has estimated that in 2020 there were approximately 9,100
hospital-based laboratories, more than 121,000 physician-office laboratories and approximately 6,500 independent clinical and
anatomic pathology laboratories in the U.S. Dx competes with all of those laboratories.
Dx believes that the selection of a laboratory is primarily based on the following factors, all of which the Company believes
it competes favorably in:
•
•
•
•
•
•
•
quality, timeliness and consistency in reporting test results;
reputation of the laboratory in the medical community or field of specialty;
contractual relationships with MCOs;
service capability and convenience;
number and type of tests performed;
connectivity solutions offered; and
pricing of the laboratory’s services.
Dx believes that consolidation in the clinical laboratory testing business will continue. In addition, Dx believes that it and
other large, independent clinical laboratory testing companies will be able to increase their share of the overall clinical
laboratory testing market due to a number of factors, including cost efficiencies afforded by large-scale automated testing,
mergers and acquisitions of complementary businesses, changes in payment models to performance and value-based
reimbursement to deliver better outcomes at lower cost, and the increasing importance of large, integrated service networks. In
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addition, legal restrictions on physician referrals and physician ownership of laboratories, as well as ongoing regulation of
laboratories, are expected to continue to contribute to the ongoing consolidation of the industry.
DD
Drug development services companies like DD are also referred to as CROs and typically derive substantially all of their
revenue from research and development (R&D), as well as marketing expenditures, of the biopharmaceutical industry.
Outsourcing of R&D services by biopharmaceutical companies to CROs has increased in the past, and is expected to
continue increasing in the future. Increasing pressures to improve return on investment, to increase R&D productivity, to stay
abreast of scientific advances and to comply with stringent government regulations have all contributed to this outsourcing to
CROs. A CRO provides biopharmaceutical companies flexibility in aligning resources to demand. In the face of mounting
complexity, the investment and amount of time required to develop new products are significant and have been increasing.
These trends create opportunities for DD and other CROs that can help make the development process more efficient.
The drug development industry has many participants ranging from hundreds of small providers to a limited number of large
CROs with global capabilities. DD competes against these small and large CROs, as well as in-house departments of
biopharmaceutical, medical device and diagnostic companies, and to a lesser extent, selected academic research centers,
universities and teaching hospitals.
DD believes that customers selecting a CRO often consider the following factors, all of which the Company believes it
competes favorably in:
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
reputation for quality and regulatory compliance;
efficient, timely performance;
expertise and experience in operations;
application of technology and innovation;
specific therapeutic and scientific expertise;
data and analytical capabilities;
post approval and market access services;
ability to recruit patients;
scope of service offerings;
strengths in various geographic markets;
price;
quality of facilities;
quality of relationships, including investigator and patient;
ability to manage large-scale clinical trials both domestically and internationally, including the recruitment of
appropriate and sufficient clinical trial subjects;
size and scale; and
access to talent.
Quality
Dx and DD have comprehensive quality systems and processes appropriate for their respective businesses. The Company's
quality programs are overseen by Dx's National Office of Quality, DD’s Global Regulatory Compliance and Quality Assurance
Unit, DD's clinical trial services global vendor management department, DD's central laboratory services expanded laboratory
management services department, and the Company's global supply chain management department and project management
staff. The Company has procedures for monitoring its internal performance, as well as that of its vendors, suppliers, and other
key stakeholders. In addition, various groups and departments within the Company provide oversight to monitor and control
vendor products and performance, and play an essential role in the Company’s approach to quality through improvements in
processes and automation.
Virtually all facets of the Company’s services are subject to quality programs and procedures, including accuracy and
reproducibility of tests; turnaround time; customer service; data integrity; patient satisfaction; and billing. The Company’s
quality program includes measures that compare current performance against desired performance goals to monitor critical
aspects of service to its customers and patients. This includes licensing, credentialing, training and competency of professional
and technical staff, and internal auditing. In addition to the Company's own quality programs, the Company’s laboratories,
facilities and processes are subject to on-site regulatory agency inspections and accreditation evaluations, in addition to surveys
and proficiency testing, by local or national government agencies; independent external accrediting programs; and inspections
and audits by customers.
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Thirty-four of the Company's laboratories have received ISO-15189 accreditation, demonstrating that they meet
international standards for quality and technical competence.
Information Systems
The Company is committed to developing and commercializing technology-enabled solutions to support its operations and
provide better care. The Company operates standard platforms for its core business services and its financial and reporting
systems. These standard systems provide consistency within workflows and information as well as a high level of system
availability, security, and stability. The primary laboratory systems include standardized support for molecular diagnostics,
digital pathology and enhanced specialty laboratory solutions. The Company's centralized information systems are responsible
for tremendous operational efficiencies, enabling the Company to achieve consistent, structured, and standardized operating
results and superior patient care.
In addition, Dx and DD each offer proprietary and industry-leading information systems, which are discussed in more detail
in the sections dedicated to each of those segments.
Intellectual Property Rights
The Company relies on a combination of patents, trademarks, copyrights, trade secrets, and nondisclosure and non-
competition agreements to establish and protect its proprietary technology. The Company has filed and obtained numerous
patents in the U.S. and abroad, and regularly files patent applications, when appropriate, to establish and protect its proprietary
technology. Occasionally, the Company also licenses U.S. and non-U.S. patents, patent applications, technology, trade secrets,
know-how, copyrights or trademarks owned by others. The Company believes, however, that no single patent, technology,
trademark, intellectual property asset or license is material to its business as a whole.
Patents covering the Company's technologies are subject to challenges. Issued patents may be successfully challenged,
invalidated, circumvented, or declared unenforceable so that patent rights would not create an effective competitive barrier. In
addition, the laws of some countries may not protect proprietary rights to the same extent as do the laws of the U.S.
Parties may file claims asserting that the Company's technologies infringe on their intellectual property. The Company
cannot predict whether parties will assert such claims against it, or whether those claims will harm its business. If the Company
is forced to defend against such claims, the Company could face costly litigation and diversion of management’s attention and
resources. As result of such disputes, the Company may have to develop costly non-infringing technology or enter into
licensing agreements. These agreements, if necessary, may require financial or other terms that could have an adverse effect on
the Company's business and financial condition.
Regulation and Reimbursement
General
Because the Company operates in a number of distinct environments and in a variety of locations worldwide, it is subject to
numerous, and sometimes overlapping, regulatory requirements. Both the clinical laboratory industry and the drug development
business are subject to significant governmental regulation at the national, state and local levels. As described below, these
regulations concern licensure and operation of clinical laboratories, claim submission and reimbursement for laboratory
services, healthcare fraud and abuse, drug development services, security and confidentiality of health information, quality, and
environmental and occupational safety.
Regulation of Clinical Laboratories
Virtually all clinical laboratories operating in the U.S. must be certified by the federal government or by a federally
approved accreditation agency. In most cases, that certification is regulated by CMS through CLIA, which requires that
applicable clinical laboratories meet quality assurance, quality control, and personnel standards. Laboratories also must undergo
proficiency testing and are subject to inspections. Clinical laboratories in locations other than the U.S. are generally subject to
comparable regulation in their respective jurisdictions.
Standards for testing under CLIA are based on the complexity of the tests performed by the laboratory, with tests classified
as “high complexity,” “moderate complexity,” or “waived.” Laboratories performing high-complexity testing are required to
meet more stringent requirements than moderate-complexity laboratories. Laboratories performing only waived tests, which are
tests determined by the FDA to have a low potential for error and requiring little oversight, may apply for a certificate of waiver
exempting them from most CLIA requirements. All major and many smaller Company facilities hold CLIA certificates to
perform high-complexity testing. The Company's remaining smaller testing sites hold CLIA certificates to perform moderate-
complexity testing or a certificate of waiver. The sanctions for failure to comply with CLIA requirements include suspension,
revocation, or limitation of a laboratory's CLIA certificate, which is necessary to conduct business; cancellation or suspension
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of the laboratory's approval to receive Medicare and/or Medicaid reimbursement; as well as significant fines and/or criminal
penalties. The loss or suspension of a CLIA certification, imposition of a fine or other penalties, or future changes in the CLIA
law or regulations (or interpretation of the law or regulations) could have a material adverse effect on the Company.
The Company is also subject to state and local laboratory regulation. CLIA provides that a state may adopt laboratory
regulations different from or more stringent than those under federal law, and a number of states have implemented their own
laboratory regulatory requirements. State laws may require that laboratory personnel meet certain qualifications, specify certain
quality controls, or require maintenance of certain records.
The Company believes that it is in compliance in all material respects with all laboratory requirements applicable to its
laboratories operating both within the U.S. and in other countries. The Company's laboratories have continuing programs to
maintain operations in compliance with all such regulatory requirements, but no assurances can be given that the Company's
laboratories will pass all future licensure or certification inspections.
FDA and Other Regulatory Agency Laws and Regulations
Various regulatory agencies, including the FDA in the U.S., have regulatory responsibility over the development, testing,
manufacturing, labeling, advertising, marketing, distribution, storage, import, export, and surveillance of diagnostic and
therapeutic products and services, including certain products and services offered by the Company, and the development of
therapeutic products that comprise the majority of DD’s business. The FDA and other regulatory agencies periodically inspect
and review the manufacturing processes and product performance of diagnostic and therapeutic products. The FDA and other
regulatory agencies also periodically inspect clinical study sites and CROs that conduct clinical trials, including test facilities
that perform tests on samples from human subjects enrolled in such clinical studies of drugs, biologics, and medical devices.
These agencies have the authority to take various administrative and legal actions for noncompliance, such as fines, withdrawal
of product approval, warning or untitled letters, seizures, recalls, injunctions and other civil and criminal sanctions. There are
similar national and regional regulatory agencies in the jurisdictions outside the U.S. in which the Company operates.
Since 2014, there have been ongoing discussions and advocacy between stakeholders, including the clinical laboratory
industry, the FDA, and Congress, about potential FDA regulation of laboratory-developed tests (LDTs), which are assays
developed and performed in-house by clinical laboratories and can be made available to the public without pre-market review
by the FDA (although COVID-19 diagnostic PCR LDTs have been subject to FDA pre-market requirements as modified by
guidance issued by FDA on February 29, 2020, as a consequence of the national health emergency). Various regulatory and
legislative proposals are under consideration, including some that could increase general FDA oversight of clinical laboratories
and LDTs. The outcome and ultimate impact of such proposals on the Company is difficult to predict at this time.
DD’s laboratory facilities and Dx's clinical laboratory facilities that perform testing in support of clinical trials, must
conform to a range of standards and regulations, including good laboratory practice (GLP) and good clinical practice (GCP),
good manufacturing practice (cGMP), human subject protection and investigational product exemption regulations, and quality
system regulation (QSR) requirements, as applicable. The preclinical and clinical studies that the Company conducts are subject
to periodic inspections by the FDA as well as other regulatory agencies in the jurisdictions outside the U.S. in which the
Company operates, which may include, without limitation, the Medicines and Healthcare products Regulatory Agency
(MHRA) in the U.K., the European Medicines Agency, the National Medical Products Administration in China, and the
Pharmaceuticals and Medical Devices Agency in Japan, to determine compliance with GLP and GCP as well as other
applicable standards and regulations. If a regulatory agency determines during an inspection that the Company’s equipment,
facilities, laboratories, operations, or processes do not comply with applicable regulations and GLP and/or GCP standards, the
regulatory agency may issue a formal notice, which may be followed by a warning letter if observations are not addressed
satisfactorily. Noncompliance may result in, among other things, unanticipated compliance expenditures, or the regulatory
agency seeking civil, criminal or administrative sanctions and/or remedies against the Company, including suspension of its
operations.
Additionally, certain DD services and activities, such as chemistry, manufacturing, and controls (CMC) services and
manufacturing of investigational medicinal products for use in certain Phase I studies managed by DD, must conform to cGMP.
DD is subject to periodic inspections by the FDA and the MHRA, as well as other regulatory agencies in the jurisdictions
outside the U.S. in which the Company operates, in order to assess, among other things, cGMP compliance. If a regulatory
agency identifies deficiencies during an inspection, it may issue a formal notice, which may be followed by a warning letter if
observations are not addressed satisfactorily. Failure to maintain compliance with cGMP regulations and other applicable
requirements of various regulatory agencies could result in, among other things, fines, warnings or untitled letters, unanticipated
compliance expenditures, suspension of manufacturing, enforcement actions, product seizures or recalls, injunctions, or
criminal prosecution.
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Animal Welfare Laws and Regulations
The conduct of animal research at DD’s facilities in the U.S. must be in compliance with the AWA, which governs the care
and use of warm-blooded animals for research in the U.S. other than laboratory rats, mice, and chickens, and is enforced
through periodic inspections by the U.S. Department of Agriculture (USDA). The AWA establishes facility standards regarding
several aspects of animal welfare, including housing, ventilation, lighting, feeding and watering, handling, veterinary care, and
recordkeeping. DD complies with licensing and registration requirement standards set by the USDA and similar agencies in
foreign jurisdictions such as the European Union, the U.K., and China for the care and use of regulated species. If the USDA
determines that DD’s equipment, facilities, laboratories or processes do not comply with applicable AWA standards, it may
issue an inspection report documenting the deficiencies and setting deadlines for any required corrective actions. The USDA
may impose fines, suspend and/or revoke licenses and registrations, or confiscate research animals. Other countries where the
Company conducts business have similar laws and regulations with which the Company must also comply. In addition, certain
of DD’s animal-related activities may be subject to regulation by the U.S. Centers for Disease Control and Prevention (CDC),
the Office of Laboratory Animal Welfare of the National Institutes of Health, the U.S. Fish and Wildlife Service, and similar
organizations in other jurisdictions.
Payment for Clinical Laboratory Services
In 2020, Dx derived approximately 11.3% of its revenue directly from traditional Medicare and Medicaid programs. In
addition, Dx's other commercial laboratory testing business that is not directly related to Medicare or Medicaid nevertheless
depends significantly on continued participation in these programs and in other government healthcare programs, in part
because customers often want a single laboratory to perform all of their testing services. In recent years, both governmental and
private sector payers have made efforts to contain or reduce healthcare costs, including reducing reimbursement for clinical
laboratory services.
Reimbursement under the Medicare PFS is capped at different rates in each Medicare Administrative Contractor's
jurisdiction. Pursuant to PAMA, reimbursement under the CLFS is set at a national rate that is updated every three years for
most tests. State Medicaid programs are prohibited from paying more than the Medicare fee schedule limit for clinical
laboratory services furnished to Medicaid recipients. Laboratories primarily bill and are reimbursed by Medicare and Medicaid
directly for covered tests performed on behalf of Medicare and Medicaid beneficiaries; for beneficiaries that participate in
Managed Medicare and Managed Medicaid plans, laboratory bills are submitted to and paid by MCOs that manage those plans.
Approximately 8.8% of Dx's revenue is reimbursed directly by Medicare under the CLFS.
Many pathology services performed by Dx are reimbursed by Medicare under the PFS. The PFS assigns relative value units
to each procedure or service, and a conversion factor is applied to calculate the reimbursement. The PFS is also subject to
adjustment on an annual basis. Such adjustments can impact both the conversion factor and relative value units. The Sustainable
Growth Rate (SGR), the formula previously used to calculate the fee schedule conversion factor, would have resulted in
significant decreases in payment for most physician services for each year since 2003. However, Congress intervened
repeatedly to prevent these payment reductions, and the conversion factor was increased or frozen for the subsequent year. The
Medicare Access and CHIP Reauthorization Act of 2015 (MACRA) permanently replaced the SGR formula and transitioned
PFS reimbursement to a value-based payment system. MACRA retroactively avoided a 21.2% reduction in PFS reimbursement
that had been scheduled for April 1, 2015, and provided for PFS conversion factor increases of 0.5% from July 1, 2015 to
December 31, 2015, and 0.5% in each of years 2016-2019, followed by no updates for 2020-2025, and updates that vary based
on participation in alternative payment models in subsequent years. These changes to the conversion factor may be offset by
reductions to the relative value units, as was the case with the 2016 PFS reductions. Approximately 0.4% of Dx's revenue is
reimbursed under the PFS.
In addition to changes in reimbursement rates, Dx is also impacted by changes in coverage policies for laboratory tests and
annual CPT coding revisions. Medicare, Medicaid and private payer diagnosis code requirements and payment policies
negatively impact Dx's ability to be paid for some of the tests it performs. Further, some payers require additional information
to process claims, employ third-party utilization management tools, or have implemented prior authorization policies which
delay or prohibit payment. In 2020, with the exception of those specifically related to COVID-19 testing, there were limited
coding and billing changes. While limited changes are expected to be implemented in 2021, the Company typically expects
some delays in pricing and reimbursement as new codes are introduced.
Future changes in national, state and local laws and regulations (or in the interpretation of current regulations) affecting
government payment for clinical laboratory testing could have a material adverse effect on the Company.
Further healthcare reform could occur in 2021, including changes to the ACA and Medicare reform, initiatives to address
surprise billing and increased price transparency, as well as administrative requirements that may continue to affect coverage,
reimbursement, and utilization of laboratory services in ways that are currently unpredictable.
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Privacy, Security and Confidentiality of Health Information and Other Personal Information
In the U.S., the Health Insurance Portability and Accountability Act of 1996 (HIPAA) was designed to address issues
related to the security and confidentiality of health information and to improve the efficiency and effectiveness of the healthcare
system by facilitating the electronic exchange of information in certain financial and administrative transactions. These
regulations apply to health plans and healthcare providers that conduct standard transactions electronically and healthcare
clearinghouses (covered entities). Six such regulations include: (i) the Transactions and Code Sets Rule; (ii) the Privacy Rule;
(iii) the Security Rule; (iv) the Standard Unique Employer Identifier Rule, which requires the use of a unique employer
identifier in connection with certain electronic transactions; (v) the National Provider Identifier Rule, which requires the use of
a unique healthcare provider identifier in connection with certain electronic transactions; and (vi) the Health Plan Identifier
Rule, which required the use of a unique health plan identifier in connection with certain electronic transactions. The Company
believes that it is in compliance in all material respects with each of the HIPAA Rules identified above.
The Privacy Rule regulates the use and disclosure of protected health information (PHI) by covered entities. It also sets
forth certain rights that an individual has with respect to his or her PHI maintained by a covered entity, such as the right to
access or amend certain records containing PHI or to request restrictions on the use or disclosure of PHI. The Privacy Rule
requires covered entities to contractually bind third parties, known as business associates, in the event that they perform an
activity or service for or on behalf of the covered entity that involves the creation, receipt, maintenance, or transmission of PHI.
The Company believes that it is in compliance in all material respects with the requirements of the HIPAA Privacy Rule.
On February 6, 2014, CMS and HHS published final regulations that amended the HIPAA Privacy Rule to provide
individuals (or their personal representatives) with the right to receive copies of their test reports from laboratories subject to
HIPAA, or to request that copies of their test reports be transmitted to designated third parties. The Company believes its
policies and procedures and privacy notice comply with the Privacy Rule access requirements.
On December 12, 2018, HHS issued a request for information (RFI) seeking input from the public on how the HIPAA
regulations and the Privacy Rule, in particular, could be modified to amend existing, or impose additional, obligations relating
to the processing of PHI. Subsequent to the RFI, on January 21, 2021, HHS published a notice of proposed rulemaking (NPRM)
containing potential modifications to the Privacy Rule addressing standards that may impede the transition to value-based
health care. The Company is monitoring the NPRM process. If modifications to the Privacy Rule are adopted, they may impact
the Company's compliance obligations under HIPAA.
The U.S. Health Information Technology for Economic and Clinical Health Act (HITECH), which was enacted in February
2009, with regulations effective on September 23, 2013, strengthened and expanded the HIPAA Privacy and Security Rules and
their restrictions on use and disclosure of PHI. HITECH includes, but is not limited to, prohibitions on exchanging PHI for
remuneration and additional restrictions on the use of PHI for marketing. HITECH also fundamentally changes a business
associate’s obligations by imposing a number of Privacy Rule requirements and a majority of Security Rule provisions directly
on business associates that were previously only directly applicable to covered entities. Moreover, HITECH requires covered
entities to provide notice to individuals, HHS, and, as applicable, the media when unsecured PHI is breached, as that term is
defined by HITECH. Business associates are similarly required to notify covered entities of a breach. The Company believes its
policies and procedures are fully compliant with HIPAA as modified by the HITECH requirements.
The administrative simplification provisions of HIPAA mandate the adoption of standard unique identifiers for healthcare
providers. The intent of these provisions is to improve the efficiency and effectiveness of the electronic transmission of health
information. The National Provider Identifier Rule requires that all HIPAA-covered healthcare providers, whether they are
individuals or organizations, must obtain an NPI to identify themselves in standard HIPAA transactions. NPI replaces the
unique provider identification number and other provider numbers previously assigned by payers and other entities for the
purpose of identifying healthcare providers in standard electronic transactions. The Company believes that it is in compliance
with the HIPAA National Provider Identifier Rule in all material respects.
The Health Plan Identifier (HPID) was a unique identifier designed to furnish a standard way to identify health plans in
electronic transactions. CMS published the final rule adopting the HPID for health plans required by HIPAA on September 12,
2012. Effective October 31, 2014, CMS announced a delay, until further notice, in enforcement of regulations pertaining to
health plan enumeration and use of the HPID in HIPAA transactions adopted in the HPID final rule. On October 28, 2019,
CMS published a final rule rescinding the adopted standard unique HPID and implementation specifications and requirements
for its use and other entity identifier and implementation specifications for its use, effective December 27, 2019. This delay
remains in effect. The Company will continue to monitor future developments related to the HPID and respond accordingly.
Violations of the HIPAA provisions could result in civil and/or criminal penalties, including significant fines and up to 10
years in prison. HITECH also significantly strengthened HIPAA enforcement by increasing the civil penalty amounts that may
be imposed, requiring HHS to conduct periodic audits to confirm compliance and authorizing state attorneys general to bring
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civil actions seeking either injunctions or damages in response to violations of the HIPAA privacy and security regulations that
affect the privacy of state residents.
The total cost associated with meeting the ongoing requirements of HIPAA and HITECH is not expected to be material to
the Company’s operations or cash flows. However, future regulations and interpretations of HIPAA and HITECH could impose
significant costs on the Company.
In addition to the HIPAA regulations described above, numerous other data protection, privacy and similar laws govern the
confidentiality, security, use, and disclosure of personal information. These laws vary by jurisdiction, but they most commonly
regulate or restrict the collection, use, and disclosure of medical and financial information and other personal information. In
the U.S., some state laws are more restrictive and, therefore, are not preempted by HIPAA. Penalties for violation of these laws
may include sanctions against a laboratory's licensure, as well as civil and/or criminal penalties.
Congress and state legislatures also have been considering new legislation relating to privacy and data protection. For
example, on June 28, 2018, the California legislature passed the California Consumer Privacy Act (CCPA), which became
effective January 1, 2020. The CCPA created new transparency requirements and granted California residents several new
rights with regard to their personal information. In addition, in November 2020, California voters approved the California
Privacy Rights Act (CPRA) ballot initiative, which introduced significant amendments to the CCPA and established and funded
a dedicated California privacy regulator, the California Privacy Protection Agency (CPPA). The amendments introduced by the
CPRA go into effect on January 1, 2023, and new implementing regulations are expected to be introduced by the CPPA. Failure
to comply with the CCPA may result in, among other things, significant civil penalties and injunctive relief, or potential
statutory or actual damages. In addition, California residents have the right to bring a private right of action in connection with
certain types of incidents. These claims may result in significant liability and potential damages. The Company implemented
processes to manage compliance with the CCPA and continues to assess the impact of the CPRA on the Company’s business as
additional information and guidance becomes available.
Effective August 14, 2020, the Substance Abuse and Mental Health Services Administration of HHS (SAMHSA)
announced the finalization of proposed changes to the Confidentiality of Substance Use Disorder Patient Records regulation, 42
Code of Federal Regulations Part 2. This regulation protects the confidentiality of patient records relating to the identity,
diagnosis, prognosis, or treatment that are maintained in connection with the performance of any federally assisted program or
activity relating to substance use disorder education, prevention, training, treatment, rehabilitation, or research. Under the
regulation, patient identifying information may only be released with the individual’s written consent, subject to certain limited
exceptions. The latest changes to this regulation seek to better facilitate care coordination, while maintaining more stringent
confidentiality of substance use disorder information. The Company adopted changes to its policies and procedures necessary
for compliance.
The European Union General Data Protection Regulation (GDPR) Regulation (EU) 2016/679, became effective May 25,
2018, replacing Directive 95/46/EC. The GDPR established requirements applicable to the use and transfer of personal data and
imposes penalties for noncompliance of up to the greater of €20 million or 4% of worldwide revenue. The GDPR requires
transparency with regard to the means and purposes of processing of personal data; collection of consent to process personal
data in certain circumstances; the ability to provide records of processing upon request by a supervisory authority or data
controller; implementation of appropriate technical and organizational measures to maintain security of personal data;
notification of personal data breaches to supervisory authorities, data controllers, and individuals within expedient time frames;
and performance of data protection impact assessments for certain processing activities. Personal data may only be transferred
outside of the European Union to a country that offers an adequate level of data protection under standards set by the European
Union. The GDPR also provides individual data subjects with certain rights, where applicable, including the right of access, the
right to rectification, the right to be forgotten, the right to restrict or object to processing, and the right to data portability. The
Company has established processes and frameworks to manage compliance with the GDPR and other global privacy and data
protection requirements, and to manage preparation for future enacted regulations. Compliance could impose significant costs
on the Company.
In addition to the GDPR, numerous other countries have laws governing the collection, use, disclosure, and transmission
(including cross-border transfer) of personal information, including medical information. The legislative and regulatory
landscape for privacy and data protection is complex and continually evolving. Data protection regulations have been enacted
or updated in regions where the Company does business including in Asia, Latin America, and Europe, and in countries such as
Canada and the UK. Failure to comply with these regulations may result in, among other things, civil, criminal and contractual
liability, fines, regulatory sanctions and damage to the Company’s reputation.
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Fraud and Abuse Laws and Regulations
Existing U.S. laws governing federal healthcare programs, including Medicare and Medicaid, as well as similar state laws,
impose a variety of broadly described fraud and abuse prohibitions on healthcare providers, including clinical laboratories.
These laws are interpreted liberally and enforced aggressively by multiple government agencies, including the U.S. Department
of Justice, OIG and various state agencies. Historically, the clinical laboratory industry has been the focus of major
governmental enforcement initiatives. The U.S. government's enforcement efforts have been conducted under regulations such
as HIPAA, which includes several provisions related to fraud and abuse enforcement, including the establishment of a program
to coordinate and fund U.S., state and local law enforcement efforts, and the Deficit Reduction Act of 2005, which includes
requirements directed at Medicaid fraud, including increased spending on enforcement and financial incentives for states to
adopt false claims act provisions similar to the U.S. False Claims Act. Amendments to the False Claims Act, and other
enhancements to the U.S. fraud and abuse laws enacted as part of the ACA, have further increased fraud and abuse enforcement
efforts and compliance risks. For example, the ACA established an obligation to report and refund overpayments from
Medicare or Medicaid within 60 days of identification (whether or not paid through any fault of the recipient); failure to comply
with this requirement can give rise to additional liability under the False Claims Act and Civil Monetary Penalties statute.
The U.S. Anti-Kickback Statute prohibits knowingly providing anything of value in return for, or to induce the referral of,
Medicare, Medicaid or other U.S. healthcare program business. Violations can result in imprisonment, fines, penalties, and/or
exclusion from participation in U.S. healthcare programs. The OIG has published “safe harbor” regulations that specify certain
arrangements that are protected from prosecution under the Anti-Kickback Statute if all conditions of the relevant safe harbor
are met. Failure to fit within a safe harbor does not necessarily constitute a violation of the Anti-Kickback Statute; rather, the
arrangement would be subject to scrutiny by regulators and prosecutors and would be evaluated on a case-by-case basis. Many
states have their own Medicaid anti-kickback laws, and several states also have anti-kickback laws that apply to all payers (i.e.,
not just government healthcare programs).
From time to time, the OIG issues alerts and other guidance on certain practices in the healthcare industry that implicate the
Anti-Kickback Statute or other fraud and abuse laws. OIG Special Fraud Alerts and Advisory Opinions relevant to the
Company set forth a number of practices allegedly engaged in by some clinical laboratories and healthcare providers that raise
issues under the U.S. fraud and abuse laws, including the Anti-Kickback Statute. These practices include: (i) providing
employees to furnish valuable services for physicians (other than collecting patient specimens for testing) that are typically the
responsibility of the physicians’ staff; (ii) offering certain laboratory services at prices below fair market value in return for
referrals of other tests that are billed to Medicare at higher rates; (iii) providing free testing to physicians’ managed care patients
in situations where the referring physicians benefit from such reduced laboratory utilization; (iv) providing free pickup and
disposal of biohazardous waste for physicians for items unrelated to a laboratory’s testing services; (v) providing general-use
facsimile machines or computers to physicians that are not exclusively used in connection with the laboratory services; (vi)
providing free testing for healthcare providers, their families and their employees (i.e., so-called “professional courtesy”
testing); (vii) compensation paid by laboratories to physicians for blood specimen processing and for submitting patient data to
registries; and (viii) the provision of discounts on laboratory services billed to customers in return for the referral of U.S.
healthcare program business.
In addition to the Anti-Kickback Statute, in October 2018, the U.S. enacted the Eliminating Kickbacks in Recovery Act of
2018 (EKRA), as part of the Substance Use-Disorder Prevention that Promotes Opioid Recovery and Treatment for Patients and
Communities Act (SUPPORT Act). EKRA is an all-payer anti-kickback law that makes it a criminal offense to pay any
remuneration to induce referrals to, or in exchange for, patients using the services of a recovery home, a substance use clinical
treatment facility, or laboratory. Although it appears that EKRA was intended to reach patient brokering and similar
arrangements to induce patronage of substance use recovery and treatment, the language in EKRA is broadly written. As
drafted, an EKRA prohibition on incentive compensation to sales employees is inconsistent with the federal anti-kickback
statute and regulations, which permit payment of employee incentive compensation, a practice that is common in the industry.
Significantly, EKRA permits the U.S. Department of Justice to issue regulations clarifying EKRA’s exceptions or adding
additional exceptions, but such regulations have not yet been issued. The Company is working through its trade association to
address the scope of EKRA and is seeking clarification or correction.
Enrollment and re-enrollment in U.S. healthcare programs, including Medicare and Medicaid, are subject to certain
program integrity requirements intended to protect the programs from fraud, waste, and abuse. In September 2019, CMS
published a final rule implementing program integrity enhancements to provider enrollment requiring Medicare, Medicaid, and
Children’s Health Insurance Program (CHIP) providers and suppliers to disclose on an enrollment application or a revalidation
application any current or previous direct or indirect affiliation with a provider or supplier that (1) has uncollected debt; (2) has
been or is subject to a payment suspension under a federal health care program; (3) has been or is excluded by the OIG from
Medicare, Medicaid, or CHIP; or (4) has had its Medicare, Medicaid, or CHIP billing privileges denied or revoked. This rule
permits CMS to deny enrollment based on such an affiliation when CMS determines that the affiliation poses an undue risk of
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fraud, waste, or abuse. CMS is phasing in this new affiliation disclosure requirement.
Under another U.S. statute, known as the Stark Law or “physician self-referral” prohibition, physicians who have a
financial or a compensation relationship with a commercial laboratory may not, unless an exception applies, refer Medicare or
Medicaid patients for testing to the laboratory, regardless of the intent of the parties. Similarly, laboratories may not bill
Medicare or Medicaid for services furnished pursuant to a prohibited self-referral. There are several Stark Law exceptions that
are relevant to arrangements involving clinical laboratories, including: i) fair market value compensation for the provision of
items or services; ii) payments by physicians to a laboratory for commercial laboratory services; iii) ancillary services
(including laboratory services) provided within the referring physician's own office, if certain criteria are satisfied; iv) physician
investment in a company whose stock is traded on a public exchange and has stockholder equity exceeding $75.0 million; and
v) certain space and equipment rental arrangements that are set at a fair market value rate and satisfy other requirements. Many
states have their own self-referral laws as well, which in some cases apply to all patient referrals, not just government
reimbursement programs.
In December 2020, the OIG and CMS published final rules to amend the regulations implementing the Anti-Kickback Statute
and the Stark Law, respectively. The amendments are primarily intended to alleviate perceived impediments to coordinated care
and value-based compensation arrangements through new safe harbors to the Anti-Kickback Statute and new exceptions to the
Stark Law, and have varying degrees of applicability to laboratories. The CMS final rule incorporates laboratories and permits
support for value-based arrangements, under certain conditions for purposes of the Stark Law. However, the OIG final rule
excludes laboratories from protection under the Anti-Kickback Statute safe harbors for value-based arrangements.
There are a variety of other types of U.S. and state fraud and abuse laws, including laws prohibiting submission of false or
fraudulent claims. The Company seeks to conduct its business in compliance with all U.S. and state fraud and abuse laws. The
Company is unable to predict how these laws will be applied in the future, and no assurances can be given that its arrangements
will not be subject to scrutiny under such laws. Sanctions for violations of these laws may include exclusion from participation
in Medicare, Medicaid, and other U.S. or state healthcare programs, significant criminal and civil fines and penalties, and loss
of licensure. Any exclusion from participation in a U.S. healthcare program, or material loss of licensure, arising from any
action by any federal or state regulatory or enforcement authority, would likely have a material adverse effect on the Company's
business. In addition, any significant criminal or civil penalty resulting from such proceedings could have a material adverse
effect on the Company's business.
Environmental, Health, and Safety
The Company is subject to licensing and regulation under laws and regulations relating to the protection of the
environment, and human health and safety laws and regulations relating to the handling, transportation and disposal of medical
specimens and hazardous materials, infectious and hazardous waste and radioactive materials. All Company laboratories are
subject to applicable laws and regulations relating to biohazard disposal of all laboratory specimens, and the Company
generally utilizes outside vendors for disposal of such specimens. In addition, the U.S. Occupational Safety and Health
Administration (OSHA) has established extensive requirements relating to workplace safety for healthcare employers, including
clinical laboratories, whose workers may be exposed to blood-borne pathogens such as HIV, HCV and hepatitis B virus (HCB).
These regulations, among other things, require work practice controls, protective clothing and equipment, training, medical
follow-up, vaccinations, and other measures designed to minimize exposure to, and transmission of, blood-borne pathogens.
Other countries where the Company conducts business have similar laws and regulations concerning the environment and
human health and safety with which the Company must also comply.
The Company is committed to reducing its carbon footprint. Energy-saving measures are continuing at Company facilities,
including installation of energy-saving LED lighting, engaging in waste-to-energy projects, and helping reduce waste going to
landfills, as well as capital investments to systems to improve energy and water usage. Funding for these and similar projects
continued through 2020 and are continuing in 2021.
The Company seeks to comply with all relevant environmental and human health and safety laws and regulations. Failure to
comply could subject the Company to various administrative and/or other enforcement actions.
Drug Testing
Drug testing for public sector employees is regulated by the SAMHSA, which has established detailed performance and
quality standards that laboratories must meet to be approved to perform drug testing on employees of U.S. government
contractors and certain other entities. To the extent that the Company’s laboratories perform such testing, each must be certified
as meeting SAMHSA standards. The Company’s laboratories in Research Triangle Park, North Carolina; Raritan, New Jersey;
Houston, Texas; Southaven, Mississippi; Spokane, Washington; and St. Paul, Minnesota are all SAMHSA certified.
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Controlled Substances
DD handles controlled substances as part of the services it provides in preclinical testing and clinical trials. The use of
controlled substances in testing for drugs of abuse is regulated by the U.S. Drug Enforcement Administration. The Company
seeks to conduct its business in compliance with these regulations as applicable. Violations of these rules may result in criminal
and civil fines and penalties.
Compliance Program
The Company maintains a comprehensive, global compliance program that includes ongoing evaluation and monitoring of
its compliance with the laws and regulations of the U.S. and the other countries in which it has operations. The objective of the
Company’s compliance program is to develop, implement, monitor, and update compliance safeguards, as appropriate.
Although the Company is subject to a broad range of regulations, its compliance program has a particular focus on regulations
related to healthcare fraud and abuse, anti-kickback, physician self-referral, government reimbursement programs, anti-bribery/
anti-corruption, anti-human trafficking and trade sanctions, among others. Emphasis is placed on developing and implementing
compliance policies and guidelines, personnel training programs, monitoring and auditing activities, and providing systems for
reporting and investigation of potential or actual compliance concerns. The compliance program demonstrates the Company's
commitment to conducting business at the highest standards of ethical conduct and integrity.
The Company seeks to conduct its business in compliance with all statutes, regulations, and other requirements applicable
to its clinical laboratory operations and drug development business. The clinical laboratory industry and drug development
industries are, however, subject to extensive regulation, and many of these statutes and regulations have not been interpreted by
the courts. In addition, the applicability or interpretation of statutes and regulations may not be clear in light of emerging
changes in clinical testing science, healthcare technology, and healthcare organizations. Applicable statutes and regulations may
be interpreted or applied by a prosecutorial, regulatory or judicial authority in a manner that would materially adversely affect
the Company. Potential sanctions for violation of these statutes and regulations include significant civil and criminal penalties,
fines, exclusion from participation in governmental healthcare programs, and the loss of various licenses, certificates, and
authorizations necessary to operate, as well as potential liabilities from third-party claims, all of which could have a material
adverse effect on the Company’s business.
Information Security
Information security is one of the Company's top priorities. Securing personal and health information is critical to the
Company’s business operations and to future growth, as the Company is committed to using technology to improve the
delivery of care. A security breach could have a material adverse operational, financial, regulatory, and reputational impact to
the Company. The Company employs a secure technology framework that enables continuous operations of laboratory
devices, computers, and communications systems. The Company has experienced and expects to continue to confront attempts
by cybercriminals who seek access to its systems and data.
The Company uses state-of-the art tools and advanced analytics to proactively identify and protect against potential
information system disruptions and breaches; to monitor, test and secure key networks and services; and to facilitate prompt
resumption of operations if a system disruption or interruption should occur. The Company has implemented policies and
procedures designed to comply with global laws and regulations related to the privacy and security of personal or health
information. In addition, the Company follows protocols for evaluating the cybersecurity status of vendors or third-parties that
will have access to the Company's data or information technology systems. The Company also carries cybercrime and business
interruption insurance.
Over the past several years, the Company has significantly increased its investment in cybersecurity technology and
training to help protect its information technology systems and operations in response to the ever-evolving cyber threat
landscape. Additional resources have been and will be dedicated to expanding the Company’s ability to investigate and
remediate any cybersecurity vulnerabilities, and to manage any impact of a cybersecurity event on its business and operations.
In July 2018, the Company experienced a ransomware incident which affected certain Dx information technology systems.
The incident temporarily affected test processing and customer access to test results, and also affected certain other
information technology systems involved in conducting Company-wide operations. The investigation determined that the
ransomware did not and could not transfer patient or client data outside of Company systems and that there was no theft or
misuse of patient or client data.
The Company is also exposed to risks related to information security arising from the information technology systems and
operations of third parties, including those of the Company's vendors and partners. For example, on May 14, 2019, Retrieval-
Masters Credit Bureau, Inc. d/b/a/ American Medical Collections Agency (AMCA), an external collection agency, notified the
Company about a security incident AMCA experienced that may have involved certain personal information about some of the
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Company's patients (the AMCA Incident). The Company referred patient balances to AMCA only when direct collection
efforts were unsuccessful. The Company's systems were not impacted by the AMCA Incident. Upon learning of the AMCA
Incident, the Company promptly stopped sending new collection requests to AMCA and stopped AMCA from continuing to
work on any pending collection requests on behalf of the Company. AMCA informed the Company that it appeared that an
unauthorized user had access to AMCA's system between August 1, 2018 and March 30, 2019, and that AMCA could not rule
out the possibility that personal information on AMCA's system was at risk during that time period. Information on AMCA's
affected system from the Company may have included name, address, and balance information for the patient and person
responsible for payment, along with the patient's phone number, date of birth, referring physician, and date of service. The
Company was later informed by AMCA that health insurance information may have been included for some individuals, and
because some insurance carriers utilize the Social Security Number as a subscriber identification number, the Social Security
Number for some individuals may also have been affected. No ordered tests, laboratory test results, or diagnostic information
from the Company were in the AMCA affected system. The Company notified individuals for whom it had a valid mailing
address. For the individuals whose Social Security Number was affected, the notice included an offer to enroll in credit
monitoring and identity protection services that will be provided free of charge for 24 months. The Company has incurred, and
expects to continue to incur, costs related to the AMCA Incident. The Company is involved in pending and threatened
litigation related to the AMCA Incident, as well as various government and regulatory inquiries and processes. For additional
information about the AMCA Incident, see Note 16 Commitments and Contingencies to the Consolidated Financial
Statements.
Item 1A.
Risk Factors
Investors should carefully consider all of the information set forth in this Annual Report, including the following risk
factors, before deciding to invest in any of the Company’s securities. The risks below are not the only ones that the Company
faces. Additional risks not presently known to the Company, or that it presently deems immaterial, may also negatively impact
the Company. The Company’s business, consolidated financial condition, revenues, results of operations, profitability,
reputation or cash flows could be materially impacted by any of these factors.
Risks Related to the COVID-19 Pandemic
The effects of the outbreak of the COVID-19 pandemic could have material adverse impacts on the Company’s
business, results of operations, cash flows, and financial position.
The Company is closely monitoring the impact of the COVID-19 pandemic on all aspects of its business. In the second half
of March 2020, daily volume for routine tests started to decline as a result of decreased consumer demand driven by a
significant reduction in physician office visits, the cancellation of elective medical procedures, and the negative impacts on
discretionary spending resulting from the economic downturn, among other factors. In addition, the performance of the
Company’s drug development business was challenged by COVID-19 due to actions that clients have taken and are taking that
slowed clinical trial progress and the associated testing as well as restrictions in trial site access in certain countries and
interruptions in the supply chain. Given the continued unpredictability pertaining to the COVID-19 pandemic and the
corresponding government restrictions and customer behavior, the impact on the Company's business continues to be uncertain
and depends on a number of evolving factors that the Company may not be able to predict or effectively respond to.
The further spread of COVID-19, including the rise of variants, and the Company’s initiatives to help limit the spread of the
illness, will impact the Company’s ability to carry out its business as usual, which could materially adversely impact its
business and financial condition. The Company has incurred additional costs in order to provide for the safety of its employees
and the continuity of its operations, including increased frequency of deep cleaning and sanitation at each of its physical
locations, additional safety training and processes, enhanced hygiene practices and materials, flexible and remote working
where possible, and allowing for greater social distancing for the Company’s employees who must work on-site. Additionally,
the Company has made a number of changes at the Company’s patient service centers for the comfort and safety of the patients,
many of which have also increased costs for the Company. For example, the Company has set aside the first business hour of
every day for vulnerable patients, launched a mobile check-in process that allows patients to wait for their appointment from
within their car or other nearby location, and increased sanitation and disinfection in check-in areas, waiting rooms, bathrooms,
and hallways with CDC-approved disinfectants.
The Company faces increased cybersecurity risks due to the number of employees that are working remotely in regions
impacted by stay-at-home orders. Increased levels of remote access create additional opportunities for cybercriminals to exploit
vulnerabilities, and employees may be more susceptible to phishing and social engineering attempts. The Company may also be
subject to increased cyber-attacks, such as phishing attacks by threat actors using the attention placed on the pandemic as a
method for targeting the Company's personnel. In addition, technological resources may be strained due to the number of
remote users.
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Adverse changes in government and third-party payer regulations, reimbursement, or coverage policies (or in the
interpretation of current regulations) relating to COVID-19 testing could materially impact the Company's results of operations,
cash flows and financial position.
The Company expects to continue to incur additional costs, which may be significant, as it continues to implement
operational changes in response to this pandemic. Further, the COVID-19 outbreak has disrupted and could continue to disrupt
the Company’s supply chain, including by impacting its ability to secure test collection supplies, equipment and testing supplies
for its facilities, personal protective equipment for its employees in its testing locations, patient service centers, and drug
development clinics. For similar reasons, the COVID-19 pandemic has also adversely impacted, and may continue to adversely
impact, third parties that are critical to the Company’s business, including vendors, suppliers, and business partners. These
developments, and others that are difficult or impossible to predict, could materially impact the Company’s business, financial
results, cash flows, and financial position.
During 2020, the Company diverted resources to developing and enhancing the accessibility of COVID-19 testing, while at
the same time taking certain steps with respect to its business strategy in order to increase cash flexibility. For example, the
Company temporarily suspended its share repurchase program, applied a heightened threshold to acquisition activity, and
delayed some of its non-COVID-19 related capital expenditures. These measures, and any other measures the Company has
taken and will continue to take to mitigate COVID-19, may be insufficient to ensure the financial stability of the Company, or
may have other adverse impacts on the Company’s business, results of operations, cash flows, and financial position.
Additionally, if the pandemic continues for an extended period of time, the Company may be forced to prioritize its application
of resources to the continued mitigation of COVID-19, at the expense of other potentially profitable opportunities or initiatives,
such as through the development of new products or selected business acquisitions.
If the Company does not respond appropriately to the ongoing COVID-19 pandemic, or if the Company’s customers do
not perceive its response to be adequate, the Company could suffer damage to its reputation, which could adversely
affect its business.
On March 11, 2020, the outbreak of COVID-19 was declared a global pandemic and containment and mitigation measures
were recommended; six days prior to this characterization, the Company announced the availability of its Labcorp 2019 Novel
Coronavirus (COVID-19) PCR test, which detects the presence of the underlying virus that causes COVID-19, for use with
patients who meet current guidance for evaluation of infection with COVID-19. On April 9, 2020, the Company announced an
agreement to collaborate on a comprehensive U.S.-based COVID-19 patient data registry. The Company also launched a self-
collection kit for its COVID-19 PCR test under an emergency use authorization from the FDA, expanded availability of
antibody tests to detect antibodies to the virus that causes COVID-19, and launched a series of innovations to increase test
capacity, throughput, and efficiency to maximize the use of supplies. The Company performed approximately 35 million
COVID-19 tests in 2020, which represents about 31 million PCR tests and over 4 million antibody tests. As of February 25,
2021, the Company has the capacity to perform 275,000 PCR tests per day, but the Company's testing capacity is dependent on
access to multiple testing platforms and the availability of equipment and testing supplies and key personnel. The Company's
central laboratory business has also seen a significant increase in demand for sample collection supplies and kits and for clinical
trials testing, which has put some pressure on the Company's supply chain and caused some delays in delivery of kit orders and
clinical trial testing result delivery. Despite the Company's efforts to obtain adequate clinical trial kit and testing supplies and
expand its capacity to make clinical trials collection kits and perform clinical trials testing, the Company may not be successful
in meeting the increased demand, and the Company’s customers and other stakeholders may perceive the Company’s responses
to the pandemic as insufficient, inadequate or not equivalent to or better than competitors, including with respect to the
availability of testing, collection kits, and the amount of time it takes for delivery of test results or fulfillment of kit orders.
Factors that may be out of the Company’s control, such as the availability of equipment, supplies, and key personnel and
geographical changes in demand, may impact the Company’s ability to meet customer demand and the Company's other
responses to the COVID-19 pandemic, and may have an adverse effect on the Company’s operations. Any such disruptions
could result in negative publicity, and the Company could suffer damage to its reputation, which could adversely affect its
business, results of operations, cash flows, and financial position.
The success of the Company is dependent in part on the efforts of its management team and employees, and the
COVID-19 pandemic could divert or hinder the Company’s human capital resources, which may adversely affect the
Company’s operations.
The Company’s management team and employees have been acutely focused on efforts to respond to and mitigate
COVID-19, including developing COVID-19 Testing. The Company has been continuously working to increase the number of
tests that can be performed and improve the time for delivering test results. The Company’s management team is also working
closely with federal and state authorities, health officials, and other key constituencies to make testing available to patients who
meet the CDC criteria for who should be tested, and HHS guidance for prioritization of testing. These response efforts have
required, and will continue to require, a large investment of time and resources that would otherwise be focused on the
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development and growth of the Company. Further, the Company's ability to maintain and expand testing capacity depend upon
maintaining and expanding its employee population. If the Company’s management team or employees become unavailable due
to illness or from other related factors, its operations could be materially adversely affected.
The ongoing COVID-19 pandemic has created significant volatility, uncertainty, and economic disruption that could
have an adverse impact on the Company’s financial position.
While the Company believes that it maintains a solid financial position, including a strong balance sheet, investment grade
ratings, and significant access to credit, the sweeping nature of the ongoing COVID-19 pandemic has created cascading effects,
all of which are difficult to predict. The Company may also experience greater than normal impact due to fluctuations in foreign
exchange rates and interest rates, decreased sales volumes, changes in employment rates and health insurance coverage, the
speed of the anticipated recovery, the ability of its customers to pay for its services, and governmental and business reactions to
the pandemic, all of which are highly uncertain and cannot be predicted. In March of 2020, the Company implemented several
measures in order to increase cash flexibility in light of these economic uncertainties, including temporarily suspending its
share repurchase program, applying a heightened threshold to acquisition activity, and delaying some of its non-COVID-19
related capital expenditures. In October of 2020, the Company reinstituted its share repurchase program. If the pandemic creates
further disruptions or turmoil in the credit and financial markets, the Company’s ability to access capital on favorable terms and
continue to meet its liquidity needs in the future could be adversely impacted which may have other adverse impacts on the
Company’s business, results of operations, cash flows, and financial position.
Risks Related to Regulatory and Compliance Matters
Changes in payer regulations or policies (or in the interpretation of current regulations or policies), insurance
regulations or approvals, or changes in other laws, regulations or policies in the U.S., may adversely affect U.S.
governmental and third-party coverage or reimbursement for clinical laboratory testing and may have a material
adverse effect upon the Company.
U.S. and state government payers, such as Medicare and Medicaid, as well as insurers, including MCOs, have increased
their efforts to control the cost, utilization and delivery of healthcare services. From time to time, Congress has considered and
implemented changes in Medicare fee schedules in conjunction with budgetary legislation. The first phase of reductions
pursuant to PAMA came into effect on January 1, 2018, and will continue annually subject to certain phase-in limits through
2025, and without limitations for subsequent periods. Further reductions due to changes in policy regarding coverage of tests or
other requirements for payment, such as prior authorization, diagnosis code and other claims edits, may be implemented from
time to time. Reimbursement for pathology services performed by Dx is also subject to statutory and regulatory reduction.
Reductions in the reimbursement rates and changes in payment policies of other third-party payers may occur as well. Such
changes in the past have resulted in reduced payments as well as added costs and have decreased test utilization for the
commercial laboratory industry by adding more complex new regulatory and administrative requirements. Further changes in
third-party payer regulations, policies, or laboratory benefit or utilization management programs may have a material adverse
effect on Dx's business. Actions by federal and state agencies regulating insurance, including healthcare exchanges, or changes
in other laws, regulations, or policies may also have a material adverse effect upon Dx's business.
The Company could face significant monetary damages and penalties and/or exclusion from government programs if it
violates anti-fraud and abuse laws.
The Company is subject to extensive government regulation at the federal, state, and local levels in the U.S. and other
countries where it operates. The Company’s failure to meet governmental requirements under these regulations, including those
relating to billing practices and financial relationships with physicians, hospitals, and health systems could lead to civil and
criminal penalties, exclusion from participation in Medicare and Medicaid and possible prohibitions or restrictions on the use of
its laboratories. While the Company believes that it is in material compliance with all statutory and regulatory requirements,
there is a risk that government authorities might take a contrary position. This risk includes, but is not limited to, the potential
that government enforcement authorities may take a contrary position with respect to the Eliminating Kickbacks in Recovery
Act, given the lack of associated regulations to clarify or add exceptions. Such occurrences, regardless of their outcome, could
damage the Company’s reputation and adversely affect important business relationships.
The Company’s business could be harmed from the loss or suspension of a license or imposition of a fine or penalties
under, or future changes in, or interpretations of, the law or regulations of CLIA, Medicare, Medicaid or other national,
state or local agencies in the U.S. and other countries where the Company operates laboratories.
The commercial laboratory testing industry is subject to extensive U.S. regulation, and many of these statutes and
regulations have not been interpreted by the courts. CLIA extends federal oversight to virtually all clinical laboratories
operating in the U.S. by requiring that they be certified by the federal government or by a federally approved accreditation
agency. The sanction for failure to comply with CLIA requirements may be suspension, revocation or limitation of a
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laboratory’s CLIA certificate, which is necessary to conduct business, as well as significant fines and/or criminal penalties. In
addition, the Company is subject to regulation under state law. State laws may require that laboratories and/or laboratory
personnel meet certain qualifications, specify certain quality controls or require maintenance of certain records. The Company
also operates laboratories outside of the U.S. and is subject to laws governing its laboratory operations in the other countries
where it operates.
Applicable statutes and regulations could be interpreted or applied by a prosecutorial, regulatory or judicial authority in a
manner that would adversely affect the Company's business. Potential sanctions for violation of these statutes and regulations
include significant fines and the suspension or loss of various licenses, certificates and authorizations, which could have a
material adverse effect on the Company’s business. In addition, compliance with future legislation could impose additional
requirements on the Company, which may be costly.
Failure to comply with privacy and security laws and regulations could result in fines, penalties and damage to the
Company’s reputation with customers and have a material adverse effect upon the Company’s business.
If the Company does not comply with existing or new laws and regulations related to protecting the privacy and security of
personal or health information, it could be subject to monetary fines, civil penalties or criminal sanctions.
In the U.S., the Health Insurance Portability and Accountability Act of 1996 (HIPAA) privacy and security regulations,
including the expanded requirements under U.S. Health Information Technology for Economic and Clinical Health Act
(HITECH), establish comprehensive standards with respect to the use and disclosure of protected health information (PHI), by
covered entities, in addition to setting standards to protect the confidentiality, integrity and security of PHI.
HIPAA restricts the Company’s ability to use or disclose PHI, without patient authorization, for purposes other than
payment, treatment or healthcare operations (as defined by HIPAA), except for disclosures for various public policy purposes
and other permitted purposes outlined in the privacy regulations. HIPAA and HITECH provide for significant fines and other
penalties for wrongful use or disclosure of PHI in violation of the privacy and security regulations, including potential civil and
criminal fines and penalties. The regulations establish a complex regulatory framework on a variety of subjects, including:
•
•
•
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•
the circumstances under which the use and disclosure of PHI are permitted or required without a specific authorization by
the patient, including, but not limited to, treatment purposes, activities to obtain payments for the Company’s services, and
its healthcare operations activities;
a patient’s rights to access, amend and receive an accounting of certain disclosures of PHI;
the content of notices of privacy practices for PHI;
administrative, technical and physical safeguards required of entities that use or receive PHI; and
the protection of computing systems maintaining electronic PHI.
The Company has implemented policies and procedures designed to comply with the HIPAA privacy and security
requirements as applicable. The privacy and security regulations establish a “floor” and do not supersede state laws that are
more stringent. Therefore, the Company is required to comply with both additional federal privacy and security regulations and
varying state privacy and security laws. In addition, federal and state laws that protect the privacy and security of patient
information may be subject to enforcement and interpretations by various governmental authorities and courts, resulting in
complex compliance issues. For example, the Company could incur damages under state laws, including pursuant to an action
brought by a private party for the wrongful use or disclosure of health information or other personal information.
The Company may also be required to comply with the data privacy and security laws of other countries in which it
operates or with which it transfers and receives data. For example, the EU's General Data Protection Regulation (GDPR), which
took effect May 25, 2018, created a range of compliance obligations for subject companies and imposes penalties for
noncompliance of up to the greater of €20 million or 4% of worldwide revenue. The Company has established processes and
frameworks to manage compliance with the GDPR. Potential fines and penalties in the event of a violation of the GDPR could
have a material adverse effect on the Company’s business and operations. In addition, similar data protection regulations
addressing access, use, disclosure and transfer of personal data have been enacted or updated in regions where the Company
does business, including in Asia, Latin America, and Europe. The Company expects to make changes to its business practices
and to incur additional costs associated with compliance with these evolving and complex regulations.
The Company's international operations could subject it to additional risks and expenses that could adversely impact
the business or results of operations.
The Company's international operations expose it to risks from potential failure to comply with foreign laws and regulations
that differ from those under which the Company operates in the U.S. In addition, the Company may be adversely affected by
other risks of expanded operations in foreign countries, including, but not limited to, changes in reimbursement by foreign
governments for services provided by the Company; compliance with export controls and trade regulations; changes in tax
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policies or other foreign laws; compliance with foreign labor and employee relations laws and regulations; restrictions on
currency repatriation; judicial systems that less strictly enforce contractual rights; countries that do not have clear or well-
established laws and regulations concerning issues relating to commercial laboratory testing or drug development services;
countries that provide less protection for intellectual property rights; and procedures and actions affecting approval, production,
pricing, reimbursement and marketing of products and services. Further, international operations could subject the Company to
additional expenses that the Company may not fully anticipate, including those related to enhanced time and resources
necessary to comply with foreign laws and regulations, difficulty in collecting accounts receivable and longer collection
periods, and difficulties and costs of staffing and managing foreign operations. In some countries, the Company's success will
depend in part on its ability to form relationships with local partners. The Company's inability to identify appropriate partners or
reach mutually satisfactory arrangements could adversely affect the business and operations.
Expanded international operations may increase the Company’s exposure to liabilities under the anti-corruption laws.
Anti-corruption laws in the countries where the Company conducts business, including the U.S. Foreign Corrupt Practices
Act (FCPA), U.K. Bribery Act, and similar laws in other jurisdictions, prohibit companies and their intermediaries from
engaging in bribery including improperly offering, promising, paying or authorizing the giving of anything of value to
individuals or entities for the purpose of corruptly obtaining or retaining business. The Company operates in some parts of the
world where corruption may be common and where anti-corruption laws may conflict to some degree with local customs and
practices. The Company maintains an anti-corruption program including policies, procedures, training and safeguards in the
engagement and management of third parties acting on the Company’s behalf. Despite these safeguards, the Company cannot
guarantee protection from corrupt acts committed by employees or third parties associated with the Company. Violations or
allegations of violations of anti-corruption laws could have a significant adverse effect on the business or results of operations.
Failure to comply with the regulations of pharmaceutical and medical device regulatory agencies, such as the FDA, the
Medicines and Healthcare Products Regulatory Agency in the United Kingdom (U.K.), the European Medicines Agency,
the National Medical Products Administration in China (NMPA), and the Pharmaceuticals and Medical Devices Agency
in Japan, could result in sanctions and/or remedies against DD and have a material adverse effect upon the Company.
The operation of DD's preclinical laboratory facilities and clinical trial operations must conform to good laboratory practice
(GLP) and good clinical practice (GCP), as applicable, as well as all other applicable standards and regulations, as further
described in Item 1 of Part I of this Annual Report. The business operations of DD’s clinical and preclinical laboratories also
require the import, export and use of medical devices, in vitro diagnostic devices, reagents, and human and animal biological
products. Such activities are subject to numerous applicable local and international regulations with which DD must comply. If
DD does not comply, DD could potentially be subject to civil, criminal or administrative sanctions and/or remedies, including
suspension of its ability to conduct preclinical and clinical studies, and to import or export to or from certain countries, which
could have a material adverse effect upon the Company.
Additionally, certain DD services and activities must conform to current good manufacturing practice (cGMP), as further
described in Item 1 of Part I of this Annual Report. Failure to maintain compliance with GLP, GCP, or cGMP regulations and
other applicable requirements of various regulatory agencies could result in warning or untitled letters, fines, unanticipated
compliance expenditures, suspension of manufacturing, and civil, criminal or administrative sanctions and/or remedies against
DD, including suspension of its laboratory operations, which could have a material adverse effect upon the Company.
Actions of animal rights activists may have an adverse effect on the Company.
DD's preclinical services utilize animals in preclinical testing of the safety and efficacy of drugs. Such activities are required
for the development of new medicines and medical devices under regulatory regimes in the U.S., Europe, Japan, and other
countries. Acts of vandalism and other acts by animal rights activists who object to the use of animals in drug development
could have an adverse effect on the Company.
Animal populations may suffer diseases that can damage DD's inventory, harm its reputation, or result in other
liability.
It is important that research products be free of diseases, including infectious diseases. The presence of diseases can distort
or compromise the quality of research results, cause loss of animals in DD’s inventory, result in harm to humans or outside
animal populations if the disease is not contained to animals in inventory, or result in other losses. Such results could harm
DD’s reputation or have an adverse effect on DD's financial condition, results of operations, and cash flows.
Failure to conduct animal research in compliance with animal welfare laws and regulations could result in sanctions
and/or remedies against DD and have a material adverse effect upon the Company.
The conduct of animal research at DD’s facilities must be in compliance with applicable laws and regulations in the
jurisdictions in which those activities are conducted. These laws and regulations include the U.S. Animal Welfare Act (AWA),
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which governs the care and use of warm-blooded animals for research in the U.S. other than laboratory rats, mice and chickens,
and is enforced through periodic inspections by the U.S. Department of Agriculture (USDA). The AWA establishes facility
standards regarding several aspects of animal welfare, including housing, ventilation, lighting, feeding and watering, handling,
veterinary care, and recordkeeping. Similar laws and regulations apply in other jurisdictions in which DD conducts animal
research, including the EU and China. DD complies with licensing and registration requirement standards set by these laws and
regulations in the jurisdictions in which it conducts animal research. If an enforcement agency determines that DD’s equipment,
facilities, laboratories or processes do not comply with applicable standards, it may issue an inspection report documenting the
deficiencies and setting deadlines for any required corrective actions. For noncompliance, the agency may take action against
DD that may include fines, suspension and/or revocation of animal research licenses, or confiscation of research animals.
U.S. FDA regulation of diagnostic products and increased FDA regulation of laboratory-developed tests (LDTs) could
result in increased costs and the imposition of fines or penalties, and could have a material adverse effect upon the
Company’s business.
The FDA has regulatory responsibility for instruments, test kits, reagents and other devices used by clinical
laboratories. The FDA enforces laws and regulations that govern the development, testing, manufacturing, performance,
labeling, advertising, marketing, distribution, and surveillance of diagnostic products, and it regularly inspects and reviews the
manufacturing processes and product performance of diagnostic products. Dx’s point-of-care testing devices are subject to
regulation by the FDA.
Since the 1990s, the FDA has asserted that it has authority to regulate LDTs as medical devices, but has exercised
enforcement discretion to refrain from systematic regulation of LDTs. In 2014, the FDA issued draft guidance describing how it
intended to discontinue its enforcement discretion policy and begin regulating LDTs as medical devices; however, that draft
guidance has not been finalized, and FDA has instead continued its enforcement discretion policy and has indicated that it
intends to work with Congress to enact comprehensive legislative reform of diagnostics oversight. As such, LDTs developed by
high complexity clinical laboratories are currently generally offered as services to health care providers under the CLIA
regulatory framework administered CMS, without the requirement for FDA clearance or approval. There are other regulatory
and legislative proposals that would increase general FDA oversight of clinical laboratories and LDTs. The outcome and
ultimate impact of such proposals on the business is difficult to predict at this time. On February 20, 2020, the FDA issued a
statement with a table of pharmacogenetic associations setting forth certain gene-drug interactions that the agency has
determined are supported by the scientific literature to help ensure that claims being made for pharmacogenetic tests are
grounded in sound science, thereby reducing the risk of enforcement actions with respect to LDTs offering claims consistent
with the table. The FDA noted that while it is committed to work with Congress on new comprehensive diagnostic oversight
reform legislation, it could still take enforcement actions under the current medical device framework regarding diagnostic
claims the agency determines not to be sufficiently supported. Even without issuance of a finalized LDT oversight framework,
in light of the April 4, 2019, FDA warning letter issued to Inova Genomics Laboratory related to certain LDTs that Inova
offered, as well as the February 2020 pharmacogenetics statement, there may be an increased risk of FDA enforcement actions
for laboratory tests offered by companies without FDA clearance or approval.
Current FDA regulation of the Company’s diagnostic products and the potential for future increased regulation of the
Company’s LDTs in the future could result in increased costs and administrative and legal actions for noncompliance, including
warning letters, fines, penalties, product suspensions, product recalls, injunctions, and other civil and criminal sanctions, which
could have a material adverse effect upon the Company.
Failure to comply with U.S., state, local or international environmental, health and safety laws and regulations,
including the U.S. Occupational Safety and Health Administration Act and the U.S. Needlestick Safety and Prevention
Act, could result in fines and penalties and loss of licensure, and have a material adverse effect upon the Company’s
business.
As previously discussed in Item 1 of Part I of this Annual Report, the Company is subject to licensing and regulation under
laws and regulations relating to the protection of the environment and human health and safety, including laws and regulations
relating to the handling, transportation and disposal of medical specimens, infectious and hazardous waste and radioactive
materials, as well as regulations relating to the safety and health of laboratory employees. Failure to comply with these laws and
regulations could subject the Company to denial of the right to conduct business, fines, criminal penalties and/or other
enforcement actions that would have a material adverse effect on its business. In addition, compliance with future legislation
could impose additional requirements on the Company that may be costly.
Risks Related to the Company's Business
General or macro-economic factors in the U.S. and globally may have a material adverse effect upon the Company,
and a significant deterioration in the economy could negatively impact testing volumes, drug development services,
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cash collections and the availability of credit.
The Company’s operations are dependent upon ongoing demand for diagnostic testing and drug development services by
patients, physicians, hospitals, MCOs, biopharmaceutical companies and others. A significant downturn in the economy could
negatively impact the demand for diagnostic testing and drug development services, as well as the ability of customers to pay
for services rendered. In addition, uncertainty in the credit markets could reduce the availability of credit and impact the
Company’s ability to meet its financing needs in the future. For additional risks, see “Risk Factors - Risks Related to the
COVID-19 Pandemic” in Part I - Item 1A.
Healthcare reform and changes to related products (e.g., health insurance exchanges), changes in government payment
and reimbursement systems, or changes in payer mix, including an increase in capitated reimbursement mechanisms
and evolving delivery models, could have a material adverse effect on the Company's revenues, profitability and cash
flow.
Dx's testing services are billed to MCOs, Medicare, Medicaid, physicians and physician groups, hospitals, patients and
employer groups. Most testing services are billed to a party other than the physician or other authorized person who ordered the
test. Increases in the percentage of services billed to government and MCOs could have an adverse effect on the Company’s
revenues.
The Company serves many MCOs. These organizations have different contracting philosophies, which are influenced by
the design of their products. Some MCOs contract with a limited number of clinical laboratories and engage in direct
negotiation of rates. Other MCOs adopt broader networks with generally uniform fee structures for participating clinical
laboratories. In some cases, those fee structures are specific to independent clinical laboratories, while the fees paid to hospital-
based and physician-office laboratories may be different, and are typically higher. MCOs may also offer Managed Medicare or
Managed Medicaid plans. In addition, some MCOs use capitation rates to fix the cost of laboratory testing services for their
enrollees. Under a capitated reimbursement arrangement, the clinical laboratory receives a per-member, per-month payment for
an agreed upon menu of laboratory tests provided to MCO members during the month, regardless of the number of tests
performed.
Capitation shifts the risk of increased test utilization (and the underlying mix of testing services) to the commercial
laboratory provider. The Company makes significant efforts to obtain adequate compensation for its services in its capitated
arrangements. For the year ended December 31, 2020, such capitated contracts accounted for approximately $319.0 million, or
3.4%, of Dx's revenues.
The Company's ability to attract and retain MCOs is critical given the impact of healthcare reform, related products and
expanded coverage (e.g. health insurance exchanges and Medicaid expansion) and evolving value-based care and risk-based
reimbursement delivery models (e.g., accountable care organizations (ACOs) and Independent Physician Associations (IPAs)).
A portion of the managed care fee-for-service revenues is collectible from patients in the form of deductibles, coinsurance
and copayments. As patient cost-sharing has been increasing, the Company's collections may be adversely impacted.
In addition, Medicare and Medicaid and private insurers have increased their efforts to control the cost, utilization and
delivery of healthcare services, including commercial laboratory services. Measures to regulate healthcare delivery in general,
and clinical laboratories in particular, have resulted in reduced prices, added costs and decreased test utilization for the
commercial laboratory industry by increasing complexity and adding new regulatory and administrative requirements. Pursuant
to legislation passed in late 2003, the percentage of Medicare beneficiaries enrolled in Managed Medicare plans has increased.
The percentage of Medicaid beneficiaries enrolled in Managed Medicaid plans has also increased, and is expected to continue
to increase; however, changes to, or repeal of, the Patient Protection and Affordable Care Act (ACA) may continue to affect
coverage, reimbursement, and utilization of laboratory services, as well as administrative requirements, in ways that are
currently unpredictable. Further healthcare reform could adversely affect laboratory reimbursement from Medicare, Medicaid or
commercial carriers.
The Company has also experienced delays in the pricing and implementation of coding and billing changes among various
payers, including Medicaid, Medicare and commercial carriers. While some delays were expected, payer policy changes in
coverage have had a negative impact on revenue, revenue per requisition, and margins and cash flows. In 2020, limited coding
and billing changes were implemented beyond those specifically related to COVID-19 Testing. While limited changes are
expected to be implemented in 2021, the Company typically expects some delays in pricing and reimbursement as new codes
are introduced.
In addition, some MCOs are implementing, directly or through third parties, various types of laboratory benefit management
programs that may include lab networks, utilization management tools (such as prior authorization and/or prior notification),
and claims edits, which may impact coverage or reimbursement for commercial laboratory tests. Some of these programs
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address commercial laboratory testing broadly, while others are focused on certain types of testing such as molecular, genetic
and toxicology testing.
The Company expects the efforts to impose reduced reimbursement, more stringent payment policies, and utilization and
cost controls by government and other payers to continue. If Dx cannot offset additional reductions in the payments it receives
for its services by reducing costs, increasing test volume, and/or introducing new services and procedures, it could have a
material adverse effect on the Company’s revenues, profitability and cash flows. In 2014, Congress passed PAMA, requiring
Medicare to change the way payment rates are calculated for tests paid under the CLFS, and to base the payment on the
weighted median of rates paid by private payers. On June 23, 2016, CMS issued a final rule to implement PAMA that required
applicable laboratories, including Dx, to begin reporting their test-specific private payer payment amounts to CMS during the
first quarter of 2017. CMS exercised enforcement discretion to permit reporting for an additional 60 days, through May 30,
2017. CMS used that private market data to calculate weighted median prices for each test (based on applicable current
procedural technology (CPT) codes) to represent the new CLFS rates beginning in 2018, subject to certain phase-in limits,
which were revised by Congress in 2019 and 2020. For 2018-2020, a test price could not be reduced by more than 10% per
year.As a result of provisions included within the CARES Act, PAMA rate reductions for 2021 have been suspended, and
therefore the Company will not experience any incremental reimbursement rate impact due to PAMA in 2021. For 2022-2024, a
test price cannot be reduced by more than 15.0% per year. The process of data reporting and repricing will be repeated every
three years for Clinical Diagnostic Laboratory Tests (CDLTs) beginning in 2022. Under current law as revised in the CARES
Act, the next data reporting period for CDLTs (based on data collected in 2019) will occur during the first quarter of 2022, and
new CLFS rates for CDLTs will be established based on that data beginning in 2023, subject to the previously described phase-
in limits. The subsequent data reporting period for CDLTs (based on data collected in 2023) will occur during the first quarter
of 2025, and new CLFS rates for CDLTs will be established based on that data beginning in 2026. CLFS rates for 2025 and
subsequent periods will not be subject to phase-in limits. CLFS rates for Advanced Diagnostic Laboratory Tests (ADLTs) will
be updated annually.
CMS published its initial proposed CLFS rates under PAMA for 2018-2020 on September 22, 2017. Following a public
comment period, CMS made adjustments and published final CLFS rates for 2018-2020 on November 17, 2017, with additional
adjustments published on December 1, 2017. For 2020, the Company realized a net reduction in reimbursement of
approximately $72.01 million from all payers affected by the CLFS (approximately $107.0 million in 2019). Unless
implementation of PAMA is further delayed or changed, an additional reduction of approximately $100.0 million is expected
for 2021, from all payers affected by the CLFS.
Healthcare reform legislation also contains numerous regulations that will require the Company, as an employer, to
implement significant process and record-keeping changes to be in compliance. These changes increase the cost of providing
healthcare coverage to employees and their families. Given the limited release of regulations to guide compliance, as well as
potential changes to the ACA, the exact impact to employers, including the Company, is uncertain.
Changes in government regulation or in practices relating to the biopharmaceutical industry could decrease the need for
certain services that DD provides.
DD assists biopharmaceutical companies in navigating the regulatory drug approval process. Changes in regulations such as
a relaxation in regulatory requirements or the introduction of simplified drug approval procedures, or an increase in regulatory
requirements that DD has difficulty satisfying or that make its services less competitive, could eliminate or substantially reduce
the demand for its services. Also, if government efforts to contain drug costs impact biopharmaceutical company profits from
new drugs, or if health insurers were to change their practices with respect to reimbursement for biopharmaceutical products,
some of DD’s customers may spend less, or reduce their growth in spending on R&D.
On December 13, 2016, the 21st Century Cures Act was signed into law. This Act provides funding designed to increase
government spending on certain drug development initiatives; contains several provisions designed to help make the drug
development process more streamlined and efficient; and allows the FDA to increase staffing to support drug development,
review and regulation. These provisions should be helpful to biopharmaceutical companies and CROs, including DD, to the
extent that they capitalize on the use of data, adaptive trial designs, real-world evidence, biomarkers and other development
tools that are accepted by the FDA.
In addition, implementation of healthcare reform legislation that adds costs could limit the profits that can be made from the
development of new drugs. This could adversely affect R&D expenditures by biopharmaceutical companies, which could in
turn decrease the business opportunities available to DD both in the U.S. and other countries. New laws or regulations may
create a risk of liability, increase DD costs or limit service offerings through DD.
Increased competition, including price competition, could have a material adverse effect on the Company’s revenues
and profitability.
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As further described in Item 1 of Part I of this Annual Report, both Dx and DD operate in highly competitive industries. The
commercial laboratory business is intensely competitive both in terms of price and service. Pricing of laboratory testing services
is often one of the most significant factors used by physicians, third-party payers and consumers in selecting a laboratory. As a
result of significant consolidation in the commercial laboratory industry, larger commercial laboratory providers are able to
increase cost efficiencies afforded by large-scale automated testing. This consolidation results in greater price competition. Dx
may be unable to increase cost efficiencies sufficiently, if at all, and as a result, its net earnings and cash flows could be
negatively impacted by such price competition. The Company may also face increased competition from companies that do not
comply with existing laws or regulations or otherwise disregard compliance standards in the industry. Additionally, the
Company may also face changes in fee schedules, competitive bidding for laboratory services, or other actions or pressures
reducing payment schedules as a result of increased or additional competition.
Competitors in the CRO industry range from hundreds of smaller CROs to a limited number of large CROs with global
capabilities. DD’s main competition consists of these small and large CROs, as well as in-house departments of
biopharmaceutical companies and, to a lesser extent, select universities and teaching hospitals. DD’s services have from time to
time experienced periods of increased price competition that had an adverse effect on a segment's profitability and consolidated
revenues and net income. There is competition among CROs for both customers and potential acquisition candidates.
Additionally, few barriers to entering the CRO industry further increases possible new competition.
These competitive pressures may affect the attractiveness or profitability of Dx’s and DD’s services, and could adversely
affect the financial results of the Company.
Failure to obtain and retain new customers, the loss of existing customers or material contracts, or a reduction in
services or tests ordered or specimens submitted by existing customers, or the inability to retain existing and/or create
new relationships with health systems could impact the Company’s ability to successfully grow its business.
To maintain and grow its business, the Company needs to obtain and retain new customers and business partners. In
addition, a reduction in tests ordered or specimens submitted by existing customers, a decrease in demand for the Company's
services from existing customers, or the loss of existing contracts, without offsetting growth in its customer base, could impact
the Company's ability to successfully grow its business and could have a material adverse effect on the Company’s revenues
and profitability. The Company competes primarily on the basis of the quality of services, reporting and information systems,
reputation in the medical community and the drug development industry, the pricing of services and ability to employ qualified
personnel. The Company's failure to successfully compete on any of these factors could result in the loss of existing customers,
an inability to gain new customers and a reduction in the Company's business.
Discontinuation or recalls of existing testing products; failure to develop or acquire licenses for new or improved
testing technologies; or the Company’s customers using new technologies to perform their own tests could adversely
affect the Company’s business.
From time to time, manufacturers discontinue or recall reagents, test kits or instruments used by the Company to perform
laboratory testing. Such discontinuations or recalls could adversely affect the Company’s costs, testing volume and revenue.
The commercial laboratory industry is subject to changing technology and new product introductions. The Company’s
success in maintaining a leadership position in genomic and other advanced testing technologies will depend, in part, on its
ability to develop, acquire or license new and improved technologies on favorable terms and to obtain appropriate coverage and
reimbursement for these technologies. The Company may not be able to negotiate acceptable licensing arrangements, and it
cannot be certain that such arrangements will yield commercially successful diagnostic tests. If the Company is unable to
license these testing methods at competitive rates, its research and development (R&D) costs may increase as a result. In
addition, if the Company is unable to license new or improved technologies to expand its esoteric testing operations, its testing
methods may become outdated when compared with the Company’s competition, and testing volume and revenue may be
materially and adversely affected.
In addition, advances in technology may lead to the development of more cost-effective technologies such as point-of-care
testing equipment that can be operated by physicians or other healthcare providers (including physician assistants, nurse
practitioners and certified nurse midwives, generally referred to herein as physicians) in their offices or by patients themselves
without requiring the services of freestanding clinical laboratories. Development of such technology and its use by the
Company’s customers could reduce the demand for its laboratory testing services and the utilization of certain tests offered by
the Company and negatively impact its revenues.
Currently, most commercial laboratory testing is categorized as high or moderate complexity, and thereby is subject to
extensive and costly regulation under CLIA. The cost of compliance with CLIA makes it impractical for most physicians to
operate clinical laboratories in their offices, and other laws limit the ability of physicians to have ownership in a laboratory and
to refer tests to such a laboratory. Manufacturers of laboratory equipment and test kits could seek to increase their sales by
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marketing point-of-care of laboratory equipment to physicians and by selling test kits approved for home or physician office use
to both physicians and patients. Diagnostic tests approved for home use are automatically deemed to be “waived” tests under
CLIA and may be performed in physician office laboratories as well as by patients in their homes with minimal regulatory
oversight. Other tests meeting certain FDA criteria also may be classified as “waived” for CLIA purposes. The FDA has
regulatory responsibility over instruments, test kits, reagents and other devices used by clinical laboratories, and it has taken
responsibility from the U.S. Centers for Disease Control and Prevention for classifying the complexity of tests for CLIA
purposes. Increased approval of “waived” test kits could lead to increased testing by physicians in their offices or by patients at
home, which could affect the Company’s market for laboratory testing services and negatively impact its revenues.
Operations may be disrupted and adversely impacted by the effects of adverse weather, other natural disasters,
geopolitical events, public health crises, and other events outside of the Company's control.
Natural disasters, such as adverse weather, fires, earthquakes, power shortages and outages, geopolitical events, such as
terrorism, war, political instability, or other conflict, criminal activities, public health crises, such as coronavirus (COVID-19)
and disease epidemics and pandemics, and other disruptions or events outside of the Company’s control could negatively affect
the Company’s operations. Any of these events may result in a temporary decline of volumes in both segments. In addition,
such events may temporarily interrupt the Company’s ability to transport specimens, the Company's ability to efficiently
commence studies, the Company’s ability to utilize information technology systems, the Company’s ability to utilize certain
laboratories, and/or the Company’s ability to receive material from its suppliers. Such events can also affect customer
operations and thereby impact testing volume. Long-term disruptions in the infrastructure and operations caused by such events
(particularly involving locations in which the Company has operations), could harm the Company's operating results. For
additional risks, see “Risk Factors - Risks Related to the COVID-19 Pandemic” in Part I - Item 1A.
Changes or disruption in services or supplies provided by third parties, including transportation, could adversely
affect the Company’s business.
The Company depends on third parties to provide services critical to the Company’s business. Although the Company has a
significant proprietary network of ground and air transport capabilities, certain of the Company's businesses are heavily reliant
on third-party ground and air travel for transport of clinical trial and diagnostic testing supplies and specimens, research
products, and people. A significant disruption to these travel systems, or the Company's access to them, could have a material
adverse effect on the Company's business. The Company is also reliant on an extensive network of third-party suppliers and
vendors of certain services and products, including for certain animal populations. Disruptions to the continued supply of these
services, products, or animal populations may arise from export/import restrictions or embargoes, political or economic
instability, pressure from animal rights activists, adverse weather, natural disasters, public health crises, transportation
disruptions, cyber attacks, or other causes, as well as from termination of relationships with suppliers or vendors for their failure
to follow the Company’s performance standards and requirements. Disruption of supply could have a material adverse effect on
the Company’s business.
A failure to identify and successfully close and integrate strategic acquisition targets could have a material adverse
effect on the Company's business objectives and its revenues and profitability.
Part of the Company's strategy involves deploying capital in investments that enhance the Company's business, which
includes pursuing strategic acquisitions to strengthen the Company's scientific capabilities and enhance therapeutic expertise,
enhance esoteric testing and global drug development capabilities, and increase presence in key geographic areas. Since 2015,
the Company has invested net cash of approximately $7.2 billion and equity of $1.8 billion in strategic business acquisitions.
However, the Company cannot assure that it will be able to identify acquisition targets that are attractive to the Company or that
are of a large enough size to have a meaningful impact on the Company's operating results. Furthermore, the successful closing
and integration of a strategic acquisition entails numerous risks, including, among others:
•
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•
•
•
•
•
•
failure to obtain regulatory clearance, including due to antitrust concerns;
loss of key customers or employees;
difficulty in consolidating redundant facilities and infrastructure and in standardizing information and other systems;
unidentified regulatory problems;
failure to maintain the quality of services that such companies have historically provided;
unanticipated costs and other liabilities;
potential liabilities related to litigation including the acquired companies;
potential periodic impairment of goodwill and intangible assets acquired;
coordination of geographically separated facilities and workforces; and
the potential disruption of the ongoing business and diversion of management's resources.
The Company cannot assure that current or future acquisitions, if any, or any related integration efforts will be successful, or
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that the Company's business will not be adversely affected by any future acquisitions, including with respect to revenues and
profitability. Even if the Company is able to successfully integrate the operations of businesses that it may acquire in the future,
the Company may not be able to realize the benefits that it expects from such acquisitions.
Continued and increased consolidation of MCOs, biopharmaceutical companies, health systems, physicians and other
customers could adversely affect the Company's business.
Many healthcare companies and providers, including MCOs, biopharmaceutical companies, health systems and physician
practices are consolidating through mergers, acquisitions, joint ventures and other types of transactions and collaborations. In
addition to these more traditional horizontal mergers that involve entities that previously competed against each other, the
healthcare industry is experiencing an increase in vertical mergers, which involve entities that previously did not offer
competing goods or services. As the healthcare industry consolidates, competition to provide goods and services may become
more intense, and vertical mergers may give those combined companies greater control over more aspects of healthcare,
including increased bargaining power. This competition and increased customer bargaining power may adversely affect the
price and volume of the Company’s services.
In addition, as the broader healthcare industry trend of consolidation continues, including the acquisition of physician
practices by health systems, relationships with hospital-based health systems and integrated delivery networks are becoming
more important. Dx has a well-established base of relationships with those systems and networks, including collaborative
agreements. Dx's inability to retain its existing relationships with those physicians as they become part of healthcare systems
and networks and/or to create new relationships could impact its ability to successfully grow its business.
Unproductive labor environments, union strikes, work stoppages, Works Council negotiations, or failure to comply with
labor or employment laws could adversely affect the Company's operations and have a material adverse effect upon the
Company's business.
The Company is a party to a limited number of collective bargaining agreements with various labor unions and is subject to
unionization activity, employment and labor laws and unionization activity in the U.S. Similar employment and labor
obligations exist across other countries in which it conducts business, including appropriate engagement with Works Councils
in Europe. Disputes with regard to the terms of labor agreements or obligations for consultation, potential inability to negotiate
acceptable contracts with these unions, unionization activity, or a failure to comply with labor or employment laws could result
in, among other things, labor unrest, strikes, work stoppages, slowdowns by the affected workers, fines and penalties. If any of
these events were to occur, or other employees were to become unionized, the Company could experience a significant
disruption of its operations or higher ongoing labor costs, either of which could have a material adverse effect upon the
Company's business. Additionally, future labor agreements, or renegotiation of labor agreements or provisions of labor
agreements, or changes in labor or employment laws, could compromise its service reliability and significantly increase its
costs, which could have a material adverse effect upon the Company's business. Also, the Company may incur substantial
additional costs and become subject to litigation and enforcement actions if the Company fails to comply with legal
requirements affecting its workforce and labor practices, including laws and regulations related to wage and hour practices,
Office of Federal Contract Compliance Programs (OFCCP) compliance, and unlawful workplace harassment and
discrimination.
An inability to attract and retain experienced and qualified personnel, including key management personnel, could
adversely affect the Company’s business.
The loss of key management personnel or the inability to attract and retain experienced and qualified employees at the
Company’s clinical laboratories, drug development, and diagnostic facilities could adversely affect the business. The success of
the Company is dependent in part on the efforts of key members of its management team. Success in maintaining the
Company’s leadership position in genomic and other advanced testing and diagnostic technologies will depend in part on the
Company’s ability to attract and retain skilled research professionals. In addition, the success of the Company’s early discovery,
clinical and commercial laboratories also depend on employing and retaining qualified and experienced professionals, including
specialists, who perform laboratory research activities and testing services. The same is true for patient-facing staff with
specialized training required to perform activities related to specimen collection or clinical research activities. In the future, if
competition for the services of these professionals increases, the Company may not be able to continue to attract and retain
individuals in its markets. Changes in key management, or the ability to attract and retain qualified personnel, could lead to
strategic and operational challenges and uncertainties, distractions of management from other key initiatives, and inefficiencies
and increased costs, any of which could adversely affect the Company’s business, financial condition, results of operations, and
cash flows.
Global economic conditions and government and regulatory changes, including, but not limited to, the U.K.'s exit from
the European Union (EU) could adversely impact the Company’s business and results of operations.
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The Company could be adversely impacted due to the consequences of changes in the economy, governments or regulations
across the globe. On January 31, 2020 the U.K. withdrew from its membership of the EU (often referred to as Brexit). The EU
and the U.K. reached an agreement in December 2020.
This type of development or other government or regulatory change could depress economic activity, which could adversely
impact the Company’s business, financial condition and results of operations. This could include long-term volatility in the
currency markets and long-term detrimental effects on the value of affected currencies.
Damage or disruption to the Company’s facilities could adversely affect the Company’s business.
Many of the Company’s facilities could be difficult to replace in a short period of time. Any event that causes a disruption of
the operation of these facilities might impact the Company's ability to provide services to customers and, therefore, could have
a material adverse effect on the Company's financial condition, results of operations, and cash flows.
Risks Related to Financial Matters
The Company bears financial risk for contracts that, including for reasons beyond the Company's control, may be
underpriced, subject to cost overruns, delayed, or terminated or reduced in scope.
The Company has many contracts that are structured as fixed-price for fixed-contracted services or fee-for-service with a
cap. The Company bears the financial risk if these contracts are underpriced or if contract costs exceed estimates. Such
underpricing or significant cost overruns could have an adverse effect on the Company's business, results of operations,
financial condition and cash flows.
Many of DD’s contracts, in particular, provide for services on a fixed-price or fee-for-service with a cap basis and they may
be terminated or reduced in scope either immediately or upon notice. Cancellations may occur for a variety of reasons,
including:
failure of products to satisfy safety requirements;
unexpected or undesired results of the products;
insufficient clinical trial subject enrollment;
insufficient investigator recruitment;
a customer's decision to terminate the development of a product or to end a particular study; and
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• DD’s failure to perform its duties properly under the contract.
Although its contracts often entitle it to receive the costs of winding down the terminated projects, as well as all fees earned
up to the time of termination, the loss, reduction in scope or delay of a large contract or the loss, delay or conclusion of
multiple contracts could materially adversely affect DD.
A significant increase in Dx's or DD's days sales outstanding could have an adverse effect on the Company’s business,
including its cash flow, by increasing its bad debt or decreasing its cash flow.
Billing for laboratory services is a complex process. Laboratories bill many different payers, including doctors, patients,
hundreds of insurance companies, Medicare, Medicaid and employer groups, all of which have different billing requirements.
In addition to billing complexities, Dx has experienced an increase in patient responsibility as a result of managed care fee-for-
service plans that continue to increase patient deductibles, coinsurance and copayments, or implement restrictive coverage or
administrative policies that can further increase patient costs. Dx expects this trend to continue. A material increase in Dx’s
days sales outstanding level could have an adverse effect on the Company's business, including potentially increasing its bad
debt rate and decreasing its cash flows. Although DD does not face the same level of complexity in its billing processes, it
could also experience delays in billing or collection, and a material increase in DD’s days sales outstanding could have an
adverse effect on the Company’s business, including potentially decreasing its cash flows.
DD’s revenues depend on the biopharmaceutical industry.
DD’s revenues depend greatly on the expenditures made by the biopharmaceutical industry in R&D. In some instances,
biopharmaceutical companies are reliant on their ability to raise capital in order to fund their R&D projects. Biopharmaceutical
companies are also reliant on reimbursement for their products from government programs and commercial payers.
Accordingly, economic factors and industry trends affecting DD’s customers in these industries may also affect DD. If these
companies were to reduce the number of R&D projects they conduct or outsource, whether through the inability to raise capital,
reductions in reimbursement from governmental programs or commercial payers, industry trends, economic conditions or
otherwise, DD could be materially adversely affected.
Foreign currency exchange fluctuations could have an adverse effect on the Company’s business.
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The Company has business and operations outside the U.S., and DD derives a significant portion of its revenues from
international operations. Since the Company's consolidated financial statements are denominated in U.S. dollars, fluctuations in
exchange rates from period to period will have an impact on reported results. In addition, DD may incur costs in one currency
related to its services or products for which it is paid in a different currency. As a result, factors associated with international
operations, including changes in foreign currency exchange rates, could significantly affect DD's results of operations, financial
condition and cash flows.
The Company’s uses of financial instruments to limit its exposure to interest rate and currency fluctuations could
expose it to risks and financial losses that may adversely affect the Company’s financial condition, liquidity and results
of operations.
To reduce the Company’s exposure to interest rate fluctuations and currency exchange fluctuations, it has entered into, and
in the future may enter into for these or other purposes, financial swaps, or hedging arrangements, with various financial
counterparties. In addition to any risks related to the counterparties, there can be no assurances that the Company’s hedging
activity will be effective in insulating it from the risks associated with the underlying transactions, that the Company would not
have been better off without entering into these hedges, or that the Company will not have to pay additional amounts upon
settlement.
The Company’s level of indebtedness could adversely affect the Company’s liquidity, results of operations and business.
At December 31, 2020, indebtedness on the Company's outstanding Senior Notes totaled approximately $5,450.0 million in
aggregate principal. The Company is also a party to credit agreements relating to a $1.0 billion revolving credit facility and a
2019 term loan with a balance of $375.0 million as of December 31, 2020. Under the term loan facility and the revolving credit
facility, the Company is subject to negative covenants limiting subsidiary indebtedness and certain other covenants typical for
investment-grade-rated borrowers, and the Company is required to maintain a leverage ratio within certain limits.
The Company’s level of indebtedness could adversely affect its business. In particular, it could increase the Company’s
vulnerability to sustained, adverse macroeconomic weakness, limit its ability to obtain further financing, and limit its ability to
pursue certain operational and strategic opportunities, including large acquisitions.
The Company may also enter into additional transactions or credit facilities, including other long-term debt, which may
increase its indebtedness and result in additional restrictions upon the business. In addition, major debt rating agencies regularly
evaluate the Company's debt based on a number of factors. There can be no assurance that the Company will be able to
maintain its existing debt ratings, and failure to do so could adversely affect the Company's cost of funds, liquidity and access
to capital markets.
The Company's quarterly operating results may vary.
The Company's operating results, may vary significantly from quarter to quarter and are influenced by factors over which
the Company has little control, such as:
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•
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changes in the general global economy;
exchange rate fluctuations;
the commencement, completion, delay or cancellation of large projects or contracts or groups of projects;
the progress of ongoing projects;
weather;
the timing of and charges associated with completed acquisitions or other events; and
changes in the utilization mix of the Company's services.
The Company believes that operating results for any particular quarter are not necessarily a meaningful indication of future
results. While fluctuations in the Company's quarterly operating results could negatively or positively affect the market price
of the Company's common stock, these fluctuations may not be related to the Company's future overall operating performance.
Risks Related to Technology and Cybersecurity
Failure to maintain the security of customer-related information or compliance with security requirements could
damage the Company’s reputation with customers, cause it to incur substantial additional costs and become subject to
litigation and enforcement actions.
The Company receives and stores certain personal and financial information about its customers. In addition, the Company
depends upon the secure transmission of confidential information over public networks, including information permitting
cashless payments. The Company also works with third-party service providers and vendors that provide technology systems
and services that are used in connection with the receipt, storage, and transmission of customer personal and financial
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information. A compromise in the Company’s security systems, or those of the Company's third party service providers and
vendors, that results in customer personal information being obtained by unauthorized persons or the Company’s or third party's
failure to comply with security requirements for financial transactions could adversely affect the Company’s reputation with its
customers and others, as well as the Company’s results of operations, financial condition and liquidity. It could also result in
litigation against the Company and the imposition of fines and penalties. For example, in connection with the AMCA Incident
the Company has incurred, and expects to continue to incur, costs, and the Company is involved in pending and threatened
litigation, as well as various government and regulatory inquiries and processes. For additional information about the AMCA
Incident, see Note 16 Commitments and Contingencies to the Consolidated Financial Statements.
Failure in the Company’s information technology systems or delays or failures in the development and implementation
of updates or enhancements to those systems could significantly increase testing turnaround time or delay billing
processes and otherwise disrupt the Company’s operations or customer relationships.
The Company’s operations and customer relationships depend, in part, on the continued performance of its information
technology systems. Despite network security measures and other precautions the Company has taken, its information
technology systems are potentially vulnerable to physical or electronic break-ins, computer viruses and similar disruptions. In
addition, the Company is in the process of integrating the information technology systems of its recently acquired subsidiaries,
and the Company may experience system failures or interruptions as a result of this process. Sustained system failures or
interruption of the Company’s systems in one or more of its operations could disrupt the Company’s ability to process
laboratory requisitions, perform testing, provide test results or drug development data in a timely manner and/or bill the
appropriate party. Failure of the Company’s information technology systems could adversely affect the Company’s business,
profitability and financial condition.
Hardware and software failures, delays in the operation of computer and communications systems, the failure to
implement new systems or system enhancements to existing systems, and cybersecurity breaches may harm the
Company.
The Company's success depends on the efficient and uninterrupted operation of its computer and communications systems.
A failure of the network or data-gathering procedures could impede the processing of data, delivery of databases and services,
customer orders and day-to-day management of the business and could result in the corruption or loss of data. While certain
operations have appropriate disaster recovery plans in place, there currently are not redundant facilities everywhere in the world
to provide information technology capacity in the event of a system failure. Despite any precautions the Company may take,
damage from fire, floods, hurricanes, power loss, telecommunications failures, computer viruses, break-ins, cybersecurity
breaches and similar events at the Company's various computer facilities could result in interruptions in the flow of data to the
servers and from the servers to customers. In addition, any failure by the computer environment to provide required data
communications capacity could result in interruptions in service. In the event of a delay in the delivery of data, the Company
could be required to transfer data collection operations to an alternative provider of server-hosting services. Such a transfer
could result in delays in the ability to deliver products and services to customers. Additionally, significant delays in the planned
delivery of system enhancements, or improvements and inadequate performance of the systems once they are completed could
damage the Company's reputation and harm the business.
Security breaches and unauthorized access to the Company's or its customers’ data could harm the Company’s
reputation and adversely affect its business.
The Company has experienced and expects to continue to experience attempts by computer programmers and hackers to
attack and penetrate the Company’s layered security controls, like the 2018 ransomware attack. The Company has also
experienced and expects to continue to experience similar attempts to attack and penetrate the systems of third-party suppliers
and vendors to whom the Company has provided data, like the 2019 data breach of Retrieval-Masters Credit Bureau, Inc. d/b/a/
American Medical Collections Agency (AMCA). These attempts, if successful, could result in the misappropriation or
compromise of personal information or proprietary or confidential information stored within the Company's systems or within
the systems of third-parties, create system disruptions or cause shutdowns. External actors are developing and deploying
viruses, worms and other malicious software programs that attack the Company’s systems, the systems of third-parties, or
otherwise exploit any security vulnerabilities. Outside parties may also attempt to fraudulently induce employees to take
actions, including the release of confidential or sensitive information or to make fraudulent payments through illegal electronic
spamming, phishing, spear phishing, or other tactics. The Company has robust information security procedures and other
safeguards in place, including evaluating the cybersecurity status of third-party suppliers and vendors that will have access to
the Company’s data or information technology systems, which are monitored and routinely tested internally and by external
parties. However, because the techniques used to obtain unauthorized access, disable or degrade service, or sabotage systems
change frequently and often are not recognized until launched against a target, the Company may be unable to anticipate all of
these techniques or to implement adequate preventive measures. In addition, as cyber threats continue to evolve, the Company
may be required to expend additional resources to continue to enhance the Company’s information security measures or to
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investigate and remediate any information security vulnerabilities. The Company’s remediation efforts may not be successful
and could result in interruptions, delays or cessation of service. This could also impact the cost and availability of cyber
insurance to the Company. Breaches of the Company’s or third-parties' security measures and the unauthorized dissemination
of personal, proprietary or confidential information about the Company or its customers or other third-parties could expose
customers’ private information. Such breaches could expose customers to the risk of financial or medical identity theft or
expose the Company or other third-parties to a risk of loss or misuse of this information, result in litigation and potential
liability for the Company, damage the Company’s brand and reputation or otherwise harm the Company’s business. Any of
these disruptions or breaches of security could have a material adverse effect on the Company’s business, regulatory
compliance, financial condition and results of operations.
The Company depends on third parties to provide services critical to the Company's business, and depends on them to
comply with applicable laws and regulations. Additionally, any breaches of the information technology systems of third
parties could have a material adverse effect on the Company's operations.
The Company depends on third parties to provide services critical to the Company's business, including supplies, ground
and air transport of clinical and diagnostic testing supplies and specimens, research products, and people, among other services.
Third parties that provide services to the Company are subject to similar risks related to security of customer-related
information and compliance with U.S., state, local, or international environmental, health and safety, and privacy and security
laws and regulations as the Company. Any failure by third parties to comply with applicable laws, or any failure of third parties
to provide services more generally, could have a material impact on the Company, whether because of the loss of the ability to
receive services from the third parties, legal liability of the Company for the actions or inactions of third parties, or otherwise.
In addition, third parties to whom the Company outsources certain services or functions may process personal data, or other
confidential information of the Company. A breach or cyber attack affecting these third parties, like the AMCA Incident, could
also harm the Company's business, results of operations and reputation.
Risks Related to Legal Matters
Adverse results in material litigation matters could have a material adverse effect upon the Company’s business.
The Company may become subject in the ordinary course of business to material legal actions related to, among other
things, intellectual property disputes, contract disputes, data and privacy issues, professional liability and employee-related
matters. The Company may also receive inquiries and requests for information from governmental agencies and bodies,
including Medicare or Medicaid payers, requesting comment and/or information on allegations of billing irregularities, billing
and pricing arrangements, or privacy practices that are brought to its attention through audits or third parties. Legal actions
could result in substantial monetary damages as well as damage to the Company’s reputation with customers, which could have
a material adverse effect upon its business.
The failure to successfully obtain, maintain and enforce intellectual property rights and defend against challenges to the
Company’s intellectual property rights could adversely affect the Company.
Many of the Company’s services, products and processes rely on intellectual property, including patents, copyrights,
trademarks and trade secrets. In some cases, that intellectual property is owned by another party and licensed to the Company,
sometimes exclusively. The value of the Company’s intellectual property relies in part on the Company’s ability to maintain its
proprietary rights to such intellectual property. If the Company is unable to obtain or maintain the proprietary rights to its
intellectual property, if it is unable to prevent attempted infringement against its intellectual property, or if it is unable to defend
against claims that it is infringing on another party’s intellectual property, the Company could be adversely affected. These
adverse effects could include the Company having to abandon, alter and/or delay the deployment of products, services or
processes that rely on such intellectual property; having to procure and pay for licenses from the holders of intellectual property
rights that the Company seeks to use; and having to pay damages, fines, court costs and attorney's fees in connection with
intellectual property litigation.
Changes in tax laws and regulations or the interpretation of such may have a significant impact on the financial
position, results of operations and cash flows of the Company.
U.S. and foreign governments continue to review, reform and modify tax laws, including with respect to the Organisation
for Economic Co-operation and Development’s base erosion and profit shifting initiative. Changes in tax laws and regulations
could result in material changes to the domestic and foreign taxes that the Company is required to provide for and pay.
In addition, the Company is subject to regular audits with respect to its various tax returns and processes in the jurisdictions
in which it operates. Errors or omissions in tax returns, process failures or differences in interpretation of tax laws by tax
authorities and the Company may lead to litigation, payments of additional taxes, penalties and interest.
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Contract research services in the drug development industry create liability risks.
In contracting to work on drug development trials and studies, DD faces a range of potential liabilities, including:
• Errors or omissions that create harm to clinical trial subjects during a trial or to consumers of a drug after the trial is
completed and regulatory approval of the drug has been granted;
• General risks associated with clinical pharmacology facilities, including negative consequences from the administration of
drugs to clinical trial participants or the professional malpractice of clinical pharmacology physicians;
• Risks that animals in DD’s facilities may be infected with diseases that may be harmful and even lethal to themselves and
humans despite preventive measures contained in DD's business policies, including those for the quarantine and handling of
imported animals; and
• Errors and omissions during a trial or study that may undermine the usefulness of a trial or study, or data from the trial or
study or that may delay the entry of a drug to the market.
DD contracts with physicians, also referred to as investigators, to conduct the clinical trials to test new drugs on clinical trial
subjects. These tests can create a risk of liability for personal injury or death to clinical trial subjects resulting from negative
reactions to the drugs administered or from professional malpractice by third party investigators.
While DD endeavors to include in its contracts provisions entitling it to be indemnified and entitling it to a limitation of
liability, these provisions are not always successfully obtained and, even if obtained, do not uniformly protect DD against
liability arising from certain of its own actions. DD could be materially and adversely affected if it were required to pay
damages or bear the costs of defending any claim that is not covered by a contractual indemnification provision, or in the event
that a party which must indemnify it does not fulfill its indemnification obligations, or in the event that DD is not successful in
limiting its liability or in the event that the damages and costs exceed DD's insurance coverage. DD may also be required to
agree to contract provisions with clinical trial sites or its customers related to the conduct of clinical trials, and DD could be
materially and adversely affected if it were required to indemnify a site or customer against claims pursuant to such contract
terms. There can be no assurance that DD will be able to maintain sufficient insurance coverage on acceptable terms.
Item 1B.
UNRESOLVED STAFF COMMENTS
None.
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Item 2.
PROPERTIES
The Company's corporate headquarters are located in Burlington, North Carolina, and include facilities that are both owned
and leased.
Labcorp Diagnostics (Dx) operates through a network of patient service centers, branches, rapid response laboratories,
primary laboratories, and specialty laboratories. The table below summarizes certain information as to Dx's principal operating
and administrative facilities as of December 31, 2020.
Location
Primary Facilities:
Birmingham, Alabama
Phoenix, Arizona
Los Angeles, California
Monrovia, California
San Diego, California
San Francisco, California
Shelton, Connecticut
Tampa, Florida
Westborough, Massachusetts
St. Paul, Minnesota
Raritan, New Jersey
Burlington, North Carolina (5)
Research Triangle Park, North Carolina (3)
Dublin, Ohio
Brentwood, Tennessee
Dallas, Texas
Houston, Texas
Herndon, Virginia
Seattle, Washington
Spokane, Washington (3)
Nature of Occupancy
Leased
Owned
Leased
Leased
Leased
Leased
Leased
Leased
Leased
Owned
Owned
Owned/Leased
Leased
Owned
Leased
Leased
Leased
Leased
Leased
Leased
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Labcorp Drug Development (DD) operates on a global scale. The table below summarizes certain information as to DD's
principal operating and administrative facilities as of December 31, 2020.
Location
Primary Facilities:
Mechelen, Belgium
Beijing, China
Shanghai, China (2)
Muenster, Germany
Pune, India
Bangalore, India
Singapore
Geneva, Switzerland
Eye, United Kingdom
Harrogate, United Kingdom
Huntingdon, United Kingdom
Leeds, United Kingdom
Maidenhead, United Kingdom
Shardlow, United Kingdom
York, United Kingdom
San Francisco, California
Daytona Beach, Florida
Greenfield, Indiana
Indianapolis, Indiana
Gaithersburg, Maryland
Ann Arbor, Michigan
Minneapolis, Minnesota
Princeton, New Jersey
Somerset, New Jersey
Dallas, Texas
Chantilly, Virginia
Madison, Wisconsin
Nature of Occupancy
Leased
Leased
Owned/Leased
Owned
Leased
Leased
Leased
Owned
Owned
Owned
Owned
Owned
Leased
Owned
Leased
Leased
Leased
Owned
Leased
Leased
Leased
Leased
Leased
Owned
Leased
Leased
Owned
All of the Company’s primary laboratory and drug development facilities have been built or improved for the purpose of
providing commercial laboratory testing or drug development services. The Company believes that these existing facilities and
plans for expansion are suitable and adequate and will provide sufficient production capacity for the Company's currently
foreseeable level of operations. The Company believes that if it were unable to renew a lease or if a lease were to be terminated
on any of the facilities it presently leases, it could find alternate space at competitive market rates and readily relocate its
operations to such new locations without material disruption to its operations.
Item 3.
LEGAL PROCEEDINGS
See Note 16 Commitments and Contingencies to the Consolidated Financial Statements.
Item 4.
MINE SAFETY DISCLOSURES
Not applicable.
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PART II
Item 5.
MARKET FOR REGISTRANT'S COMMON EQUITY, RELATED STOCKHOLDER MATTERS,
AND ISSUER PURCHASES OF EQUITY SECURITIES
Market Information
The Company's common stock, par value $0.10 per share, or Common Stock, trades on the New York Stock Exchange or
NYSE under the symbol “LH.”
Holders
On February 24, 2021, there were approximately 1,398 holders of record of the Common Stock.
Transfer Agent
The transfer agent for the Company's Common Stock is American Stock Transfer & Trust Company, Shareholder Services,
6201 Fifteenth Avenue, Brooklyn, NY 11219, telephone: 800-937-5449, website: www.amstock.com.
Dividends
The Company has not historically paid dividends on its Common Stock and does not presently anticipate paying any
dividends on its Common Stock in the foreseeable future.
Common Stock Performance
The graph below shows the cumulative total return assuming an investment of $100 on December 31, 2015, in each of the
Company’s common stock, the Standard & Poor’s, or S&P Composite-500 Stock Index and the S&P 500 Health Care Index, or
Peer Group, and assuming that all dividends were reinvested.
Comparison of Cumulative Total Return
Laboratory Corporation of America Holdings
S&P 500 Index
S&P 500 Health Care Index
$ 100.00 $ 103.83 $ 129.01 $ 102.20 $ 136.82 $ 164.63
$ 100.00 $ 111.96 $ 136.40 $ 130.42 $ 171.49 $ 203.04
97.31 $ 118.79 $ 126.47 $ 152.81 $ 173.36
$ 100.00 $
12/2015
12/2016
12/2017
12/2018
12/2019
12/2020
48
Period EndingIndex Stock PriceComparison of Cumulative Total ReturnLaboratory Corporation of America HoldingsS&P 500 IndexS&P 500 Health Care Index12/201512/201612/201712/201812/201912/202080100120140160180200220
Index
Issuer Purchases of Equity Securities (all amounts in millions, except per share amounts)
The following table sets forth information with respect to purchases of shares of the Company’s Common Stock made
during the quarter ended December 31, 2020, by or on behalf of the Company:
Total Number
of Shares
Repurchased
Average
Price Paid
Per Share
Total Number of Shares
Repurchased as Part of
Publicly Announced Program
October 1 - October 31
November 1 - November 30
December 1 - December 31
— $
—
—
— $
—
—
—
—
Maximum Dollar Value of
Shares that May Yet Be
Repurchased Under the Program
800.0
800.0
800.0
— $
—
—
—
At the end of 2019, the Company had outstanding authorization from the board of directors to purchase $900.0 of Company
common stock. During three months ended March 31, 2020, the Company purchased 0.6 shares of its common stock at an
average price of $178.85 for a total cost of $100.0. When the Company repurchases shares, the amount paid to repurchase the
shares in excess of the par or stated value is allocated to additional paid-in-capital unless subject to limitation or the balance in
additional paid-in-capital is exhausted. Remaining amounts are recognized as a reduction in retained earnings. The Company
reinstated its share repurchase program in October 2020 following the temporary suspension of stock repurchases beginning in
March 2020 as a result of the anticipated impact of the COVID-19 pandemic. At the end of 2020, the Company had outstanding
authorization from the board of directors to purchase up to $800.0 of the Company's common stock. The repurchase
authorization has no expiration date.
Item 6.
SELECTED FINANCIAL DATA (in millions, except per share amounts)
Not applicable.
Item 7.
MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS
OF OPERATIONS (in millions)
General
During the year ended December 31, 2020, the Company's revenues grew by 21.0%, due to organic growth of 19.0%,
acquisitions of 1.8% and favorable foreign currency translation of 0.4%, partially offset by the disposition of a business of
0.2%. The 19.0% increase in organic revenues includes the 24.1% contribution from PCR and antibody COVID-19 testing
(COVID-19 Testing), partially offset by the 5.1% reduction in the Company's organic Base Business due to the pandemic. Base
Business includes the Company's business operations except for COVID-19 Testing. The decline in the organic Base Business
includes the negative impact of the U.S. Protecting Access to Medicare Act of 2014 (PAMA) of 0.6%.
The Company defines organic growth as the increase in revenue excluding revenue from acquisitions for the first twelve
months after the close of each acquisition.
In March 2020, COVID-19 was declared a pandemic. COVID-19 has had and continues to have an extensive impact on the
global health and economic environments. Given the continued unpredictability of the COVID-19 pandemic and the
corresponding government restrictions and customer behavior, there are a wide-range of feasible financial results for 2021.
Throughout 2020, the Company's COVID-19 Testing has helped to offset the pressure experienced in the Base Business. To
date, the Company has performed more than 18 million PCR and 3.0 million antibody COVID-19 tests and as of February 25,
2021, has the capacity to perform 275,000 PCR and 300,000 antibody tests per day, subject to the availability of equipment and
testing supplies and key personnel.
During 2020, the Company recorded goodwill and other asset impairment charges of $462.1, $450.5 within DD and $11.6
within Dx, as a result of the COVID-19 pandemic. The Company concluded that the fair value was less than carrying value for
two of its reporting units and recorded goodwill impairment of $418.7 and $3.7 for DD and Dx, respectively. Additional
impairment of identifiable intangible and tangible assets of $31.5 and $7.9 was recorded for DD and Dx, respectively, for
impairment of a tradename, software, customer relationships, technology assets, and a note receivable.
There remains significant uncertainty regarding the duration and severity of the pandemic and its impact on the Company’s
business, results of operations and financial position for 2021. For more information regarding the risks associated with
COVID-19 and its impact on the Company’s business, see Risk Factors in Part I - Item 1A. The Company expects Phase II of
Dx’s LaunchPad initiative to deliver approximately $200.0 in net savings by the end of 2021, while incurring approximately
$40.0 in one-time implementation costs. Approximately one-third of the total savings are expected to be realized in 2021, and
one-third of the total savings have been realized in each of 2019 and 2020.
PAMA, which went into effect on January 1, 2018, resulted in a net reduction of revenue of approximately $72.0 and
$107.0 in 2020 and 2019, respectively from all payers affected by the Clinical Lab Fee Schedule.
49
Index
Results of Operations
The following tables present the financial measures that management considers to be the most significant indicators of the
Company's performance. For discussion of 2019 results and comparison with 2018 results refer to “Management's Discussion
and Analysis of Financial Conditions and Results of Operations” in the Company's Annual Report on Form 10-K for the fiscal
year ended December 31, 2019.
Years ended December 31, 2020 and 2019
Revenues
Dx
DD
Intercompany eliminations
Total
Years Ended December 31,
$
2020
9,253.4 $
4,877.7
(152.6)
2019
7,000.1
4,578.1
(23.4)
$ 13,978.5 $ 11,554.8
Change
32.2 %
6.5 %
552.1 %
21.0 %
The 21.0% increase in revenues for the year ended December 31, 2020, as compared with the corresponding period in 2019
was primarily due to organic growth of 19.0%, acquisitions of 1.8% and favorable foreign currency translation of 0.4%,
partially offset by the disposition of a business of 0.2%. The 19.0% increase in organic revenues includes the 24.1%
contribution from COVID-19 Testing, partially offset by the 5.1% reduction in the Company's organic Base Business, which
the Company believes was due to the pandemic. The decline in the organic Base Business includes the negative impact of
PAMA of 0.6%.
Dx revenues for the year ended December 31, 2020, were $9,253.4, an increase of 32.2% over revenues of $7,000.1 in the
corresponding period in 2019. The increase in revenues was due to organic growth of 30.9% and acquisitions of 1.3%. The
30.9% increase in organic revenue was due to a 39.8% contribution from COVID-19 Testing, partially offset by an 8.9%
decline of the organic Base Business which includes a 1.0% negative impact from PAMA.
Total volume, measured by requisitions, increased by 7.8% as organic volume increased by 6.5% and acquisition volume
contributed growth of 1.3%. The organic volume growth is due to demand for COVID-19 Testing of 21.2%, partially offset by
a 14.7% reduction of organic Base Business. Price/mix increased by 24.4% due to COVID-19 Testing of 18.6% and Base
Business of 5.8%. The Base Business price includes the negative impact from PAMA of 1.0%.
DD revenues for the year ended December 31, 2020, were $4,877.7, an increase of 6.5% over revenues of $4,578.1 in the
corresponding period in 2019. The increase in revenues was due to the benefit of acquisitions of 2.6%, favorable foreign
currency translation of 0.9% and organic growth of 3.5%, partially offset by a business disposition of 0.5%. The increase in
organic revenue was primarily driven by COVID-19 PCR testing through its Central Laboratories unit along with broad based
demand including COVID-19 vaccine and therapeutic work, partially offset by the negative impact from the pandemic. The
pandemic continues to cause delays in clinical trial progression and associated testing, reductions in investigator site access, as
well as interruptions to the supply chain.
Cost of Revenues
Cost of revenues
Cost of revenues as a % of revenues
Years Ended December 31,
2020
2019
Change
$ 9,025.7
64.6 %
$ 8,302.3
71.9 %
8.7 %
Cost of revenues (primarily laboratory, labor and distribution costs) increased 8.7% in 2020 as compared with 2019
primarily due to organic growth and acquisitions. Cost of revenues as a percentage of revenues decreased to 64.6% in 2020 as
compared to 71.9% in 2019. This decrease was primarily due to the impact of COVID-19 Testing on revenues and LaunchPad
savings, partially offset by PAMA and higher personnel costs (primarily driven by merit increases and one additional payroll
day that predominantly impacted Dx).
During 2020, the Company incurred special charges of $1.9 of acquisition and divestiture related costs, $36.5 in COVID-
related costs, and $1.1 related to miscellaneous other items. Additionally, the Company recorded COVID-19 related accounts
receivable reserves of $17.0, which are recorded as a reduction of revenues. Excluding these charges, cost of revenues as a
percentage of revenues were 64.2% for the year ended December 31, 2020.
50
Index
Labor and testing supplies for the year ended December 31, 2020, comprise approximately 73.0% of the Company’s cost of
revenues. Cost of revenues has increased over the two-year period ended December 31, 2020, primarily due to the impact of
acquisitions, overall growth in the Company's volume, including COVID-19 Testing, and increases in merit-based labor costs.
Selling, General and Administrative Expenses
Selling, general and administrative expenses
SG&A as a % of revenues
Years Ended December 31,
2020
$ 1,729.3
12.4 %
2019
$ 1,624.5
14.1 %
Change
6.5 %
Selling, general and administrative expenses as a percentage of revenues decreased to 12.4% in 2020 compared to 14.1% in
2019. The decrease in selling, general and administrative expenses as a percentage of revenues is primarily due to the
contribution of COVID-19 Testing on revenues and less acquisition activity.
During 2020, the Company incurred special charges of $28.3 of acquisition and divestiture related costs, $10.4 in COVID-
related costs, $14.6 in management transition costs, and $1.3 of non-capitalized costs associated with the implementation of a
major system as part of its LaunchPad business process improvement initiative, partially offset by $2.7 related to miscellaneous
other items. These items increased selling, general and administrative expenses by $51.9. Excluding these charges, selling,
general and administrative expenses as a percentage of revenues were 12.0% for the year ended December 31, 2020. The
decrease in selling, general and administrative expenses as a percentage of revenues is primarily due to leveraging the
Company's infrastructure on higher revenue, partially offset by a $15.0 initial contribution to establish the Labcorp Charitable
Foundation which supports the Company's strategic mission to improve health and improve lives with contributions focused on
health and welfare, education and community.
During 2019, the Company incurred special charges of $69.2 of acquisition and divestiture related costs, $15.2 in
management transition costs, and $10.1 of non-capitalized costs associated with the implementation of a major system as part of
its LaunchPad business process improvement initiative, partially offset by $11.7 in other miscellaneous items. These items
increased selling, general and administrative expenses by $82.9. Excluding these charges, selling, general and administrative
expenses as a percentage of revenues were 13.3% for the year ended December 31, 2019.
Goodwill and Other Asset Impairments
Goodwill and other asset impairments
Years Ended December 31,
2020
2019
$
462.1 $
—
Change
N/A
During 2020, the Company recorded goodwill and other asset impairment charges of $462.1, $450.5 within DD and $11.6
within Dx. The Company concluded that the fair value was less than carrying value for two of its reporting units and recorded
goodwill impairment of $418.7 and $3.7 for DD and Dx, respectively. Additional impairment of identifiable intangible and
tangible assets of $31.8 and $7.9 was recorded for DD and Dx, respectively, for impairment of a tradename, software, customer
relationships, technology assets and a note receivable.
Amortization Expense
Dx
DD
Amortization of intangibles and other assets
Years Ended December 31,
2020
2019
Change
$
$
104.9 $
170.5
275.4 $
102.0
141.2
243.2
2.8 %
20.8 %
13.2 %
The increase in amortization of intangibles and other assets from 2019 through 2020 primarily reflects the impact of
acquisitions partially offset by impairment of intangible assets recorded in fiscal 2020, and includes $27.5 of amortization
acceleration of certain intangible assets related to the Covance trade name as a result of the Company's rebranding initiative.
Restructuring and Other Charges
Restructuring and other charges
Years Ended December 31,
2020
2019
Change
$
40.6 $
54.6
(25.6) %
During 2020, the Company recorded net restructuring charges of $40.6; $15.3 within Dx and $25.3 within DD. The charges
were comprised of $14.1 in severance and other personnel costs $17.4 for facility, operating lease right-of-use and equipment
51
Index
impairments, and $18.9 in facility closures and general integration activities. The charges were offset by the reversal of
previously established liability of $0.6 and $9.2 in unused severance costs and facility-related costs, respectively.
During 2019, the Company recorded net restructuring charges of $54.6; $26.7 within Dx and $27.9 within DD. The charges
were comprised of $32.9 in severance and other personnel costs and $24.9 in facility-related costs primarily associated with
general integration activities. The charges were offset by the reversal of previously established liability of $1.7 in unused
severance and $1.5 in unused facility-related costs.
Interest Expense
Interest expense
Years Ended December 31,
2020
2019
Change
$
207.4 $
240.7
(13.8) %
The decrease in interest expense for 2020 as compared with the corresponding period in 2019 is primarily due to the
repayment of debt and lower interest rates.
Equity Method Income, Net
Equity method income, net
Years Ended December 31,
2020
2019
Change
$
2.9 $
9.8
(70.4) %
Equity method income, net represents the Company's ownership share in joint venture partnerships along with equity
investments in other companies in the healthcare industry. All of these partnerships and investments reside within the Dx
segment. The decrease in income for 2020 as compared with the corresponding period in 2019 was primarily due to the
impairment of an equity method investment and the decreased profitability of the Company's joint ventures.
Other, Net
Other, net
Years Ended December 31,
2020
2019
$
(32.1) $
(3.2)
Change
(903.1) %
The change in Other, net for the year ended December 31, 2020, as compared to the year ended December 31, 2019, was
primarily due to an increase in the write-off or write down of certain of the Company's investments due to the negative impact
of the COVID-19 global pandemic partially offset by lower foreign currency transaction losses. Foreign currency transaction
losses of $10.1 and $11.1 were recognized for the years ended December 31, 2020 and 2019, respectively.
Income Tax Expense
Income tax expense
Income tax expense as a % of income before tax
Years Ended December 31,
2019
2020
$
662.1
29.8 %
$
280.0
25.3 %
In 2020, the Company's effective tax rate of 29.8% was unfavorable as compared to 2019 due to impairment charges which
were not deductible and or generated tax assets which require a valuation allowance, and the geographic mix of earnings.
The Company considers substantially all of its foreign earnings to be permanently reinvested overseas.
Operating Results by Segment
Dx operating income
Dx operating margin
DD operating income
DD operating margin
General corporate expenses
Total operating income
Years Ended December 31,
2020
$ 2,634.9
28.5 %
37.3
0.8 %
$
(226.8)
$ 2,445.4
$
2019
$ 1,086.0
15.5 %
$ 411.5
9.0 %
$
(167.3)
$ 1,330.2
Change
142.6 %
13.0 %
(90.9) %
(8.2) %
35.6 %
83.8 %
52
Index
Dx operating income was $2,634.9 for the year ended December 31, 2020, an increase of 142.6% over operating income of
$1,086.0 in the corresponding period of 2019 and an increase of 1,300 basis points in operating margin year-over-year. The
increase in operating income and margin were primarily due to the increase in COVID-19 Testing and LaunchPad savings,
partially offset by a reduction in Base Business (primarily due to the pandemic), higher personnel costs and PAMA. The
Company remains on track to deliver approximately $200.0 of net savings from its three-year, Phase II of Dx’s LaunchPad
initiative by the end of 2021.
DD operating income was $37.3 for the year ended December 31, 2020, a decrease of 90.9% from operating income of
$411.5 in the corresponding period of 2019 and a decrease of 820 basis points in operating margin year-over-year. The decrease
in operating income and margin were primarily due to the negative impact of COVID-19, specifically goodwill and other asset
impairment of $450.5, and higher personnel costs, partially offset by organic demand, acquisitions, and LaunchPad savings.
The Company achieved its goal to deliver $150.0 of net savings from its three-year DD LaunchPad initiative by the end of
2020.
General corporate expenses are comprised primarily of administrative services such as executive management, human
resources, legal, finance, corporate affairs, and information technology. Corporate expenses were $226.8 for the year ended
December 31, 2020, an increase of 35.6% over corporate expenses of $167.3 in the corresponding period of 2019. The increase
in corporate expenses in 2020 is primarily due to higher personnel costs, including executive transition costs, COVID-19
related expenses and funding of the Labcorp Charitable Foundation.
Liquidity, Capital Resources and Financial Position
The Company's strong cash-generating capability and financial condition typically have provided ready access to capital
markets. The Company's principal source of liquidity is operating cash flow, supplemented by proceeds from debt offerings.
The Company's senior unsecured revolving credit facility is further discussed in Note 12 Debt to the Company's Consolidated
Financial Statements.
Management’s discussion and analysis of cash flows for the year ended December 31, 2019 compared to the year ended
December 31, 2018 may be found in the “Management’s Discussion and Analysis of Financial Condition and Results of
Operations, Liquidity, Capital Resources and Financial Position” section of the Company's Annual Report on Form 10-K for
the fiscal year ended December 31, 2019.
In summary the Company's cash flows were as follows:
Net cash provided by operating activities
Net cash (used for) provided by investing activities
Net cash used for financing activities
Effect of exchange rate on changes in cash and cash equivalents
Net change in cash and cash equivalents
Cash and Cash Equivalents
For the Year Ended December 31,
2018
2019
2020
1,305.4
2,135.3 $
206.7
(643.2)
(1,389.9)
(517.4)
(12.0)
8.6
110.2
983.3 $
1,444.7 $
(1,283.1)
(252.7)
1.8
(89.3) $
$
$
Cash and cash equivalents at December 31, 2020 and 2019 totaled $1,320.8 and $337.5, respectively. Cash and cash
equivalents consist of highly liquid instruments, such as time deposits and other money market investments, which have
original maturities of three months or less.
Cash Flows from Operating Activities
During the year ended December 31, 2020, the Company's operations provided $2,135.3 of cash as compared to $1,444.7 in
2019. The $690.6 increase in cash provided from operations in 2020 as compared with the corresponding 2019 period was
primarily due to higher cash earnings, partially offset by increased working capital to support growth. Working capital
increased primarily due to the increase in accounts receivable and supplies inventory as a result of the revenue growth, offset by
increases in income tax payable as a result of a significant increase in taxable income during the fourth quarter and an increase
in accrued payroll tax balances due to the deferral of 2020 U.S. payroll taxes as part of the CARES Act stimulus.
Cash Flows from Investing Activities
Net cash used by investing activities for the year ended December 31, 2020 was $643.2 as compared to net cash used by
investing activities of $1,283.1 for the year ended December 31, 2019. The $639.9 decrease in net cash used by investing
activities for the year ended December 31, 2020, was primarily due to a year over year decrease of $608.4 in cash paid for
acquisitions. The Company had proceeds of $7.7 from the sale of assets and disposition of businesses during 2019 in
53
Index
comparison to $42.1 during 2020. Capital expenditures were $381.7 and $400.2 for the years ended December 31, 2020 and
2019, respectively. Capital expenditures in 2020 were 2.7% of revenues, primarily in connection with projects to support
growth in the Company's core businesses, projects related to LaunchPad, and further DD acquisition integration initiatives. The
Company intends to continue to pursue acquisitions to drive growth, to make important investments in its business, including in
information technology, and to improve efficiency and enable the execution of the Company's mission. Such expenditures are
expected to be funded by cash flow from operations or, as needed, through borrowings under debt facilities, including the
Company's revolving credit facility or any successor facility. The Company expects capital expenditures in 2021 to be
approximately 4.0% of revenues, primarily in connection with projects to support growth in the Company's core businesses,
facility updates, ongoing projects related to LaunchPad within the Dx business, LaunchPad's expansion within the DD business,
and further acquisition integration initiatives.
Cash Flows from Financing Activities
Net cash used in financing activities for the year ended December 31, 2020 was $517.4 compared to cash used in financing
activities of $252.7 for the year ended December 31, 2019. This movement in cash within financing activities for 2020, as
compared to 2019, was primarily a result of $412.2 net financing payments and $100.0 in share repurchases in 2020 compared
to $198.5 in net financing receipts more than offset by $450.0 in share repurchases in 2019.
On August 17, 2020 the Company redeemed the remaining $412.2 of its 4.625% Senior Notes due November 15, 2020,
using available cash on hand. The Company exited the remaining fixed-to-variable interest rate swap agreement in August
2020, in connection with this redemption and recorded a gain of $1.6 on the extinguishment. The gain was included in Other,
net on the Consolidated Statement of Operations.
On June 3, 2019, the Company entered into a new $850.0 term loan facility in addition to the $577.0 balance then
outstanding on its existing $750.0 2017 term loan facility. The 2019 term loan facility will mature on June 3, 2021. Proceeds of
the 2019 term loan facility were used for general corporate purposes, including to repay approximately $250.0 of the 2017 term
loan facility and in connection with the acquisition of Envigo's nonclinical research services business.
On November 25, 2019, the Company issued $1,050.0 in debt securities, consisting of $400.0 aggregate principal amount
of 2.300% Senior Notes due 2024 and $650.0 aggregate principal amount of 2.950% Senior Notes due 2029. The net proceeds
from the new Senior Notes were used to redeem all of the outstanding $500.0 principal amount of its 2.625% Senior Notes due
February 1, 2020, redeem $187.9 of the outstanding 4.625% Senior Notes due November 15, 2020, and to repay $348.3
outstanding under the 2017 term loan credit facility.
In total, during 2019, the Company redeemed or repaid $687.9 million of its Senior Notes and $1,002.0 million of its term
loans. In addition, the Company borrowed and repaid a total of $495.0 million of debt through its revolving credit facility
within 2019 and $151.7 within 2020.
The Company continues to evaluate its outstanding debt portfolio to take advantage of market conditions that would allow
the Company to reduce its interest rate or financing risk and provide a lower long-term borrowing cost.
The Company's revolving credit facility consists of a five year revolving facility in the principal amount of up to $1,000.0
with the option of increasing the facility by up to an additional $350.0, subject to the agreement of one or more new or existing
lenders to provide such additional amounts and certain other customary conditions.
Under the Company's term loan credit facilities and the revolving credit facility, the Company is subject to negative
covenants limiting subsidiary indebtedness and certain other covenants typical for investment grade-rated borrowers and the
Company is required to maintain certain leverage ratios. The Company was in compliance with all covenants under the term
loan credit facility and the revolving credit facility at December 31, 2020. In May 2020, in order to obtain increased financial
covenant flexibility, the Company and its lenders entered into amendments to the term loan facility and the revolving credit
facility to increase the maximum leverage ratio to 5.0x debt to last twelve months EBITDA for the three month periods ending
June 30, September 30 and December 31, 2020, and 4.5x for the period ended March 31, 2021. From and including the period
ending June 30, 2021, the maximum leverage ratio reverts back to 4.0x. The amendments also provide that during any period in
which the Company's leverage ratio exceeds 4.5x debt to last twelve months EBITDA (i) the Company will be prohibited from
consummating share repurchases, subject to limited exceptions, (ii) borrowings under the revolving credit facility will accrue
interest at a per annum rate equal to, at the Company's election, either a LIBOR rate plus a margin of 1.25% or a base rate plus
a margin of 0.25%, (iii) the facility fee that the Company is required to pay on the aggregate commitments under the revolving
credit facility will be 0.25% per annum, and (iv) borrowings under the term loan facility will accrue interest at a per annum rate
equal to, at the Company's election, either a LIBOR rate plus a margin of 1.175% or a base rate plus a margin of 0.175%. The
Company's leverage ratio did not exceed 4.5x debt to last twelve months EBITDA as of December 31, 2020.
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Index
At the end of 2019, the Company had outstanding authorization from the board of directors to purchase up to $900.0 of
Company common stock. During 2020, the Company repurchased 0.6 shares of its common stock at an average price of
$178.85 for a total cost of $100.0. At the end of 2020, the Company had outstanding authorization from the board of directors
to purchase $800.0 of Company common stock. The repurchase authorization has no expiration date.
During 2019, the Company settled notices to convert $8.6 aggregate principal amount at maturity of its zero-coupon
subordinated notes due 2021 (the zero-coupon notes) with a conversion value of $16.6. The total cash used for these settlements
was $8.2 and the Company also issued 0.1 additional shares of common stock. As a result of these conversions in 2019, the
Company also reversed approximately $2.0 of deferred tax liability to reflect the tax benefit realized upon issuance of the
shares. On December 19, 2019, the Company redeemed any remaining outstanding zero-coupon notes that did not convert.
Credit Ratings
The Company’s investment grade debt ratings from Moody’s and BBB from Standard & Poor's (S&P) contribute to its
ability to access capital markets.
Contractual Cash Obligations
Operating lease obligations
Contingent future licensing payments (a)
Purchase obligations
Finance lease obligations
Scheduled interest payments on Senior Notes
Scheduled interest payments on Term Loan (d)
Long-term debt (e)
Total contractual cash obligations (b) (c)
Payments Due by Period
Short-term
Long-term
Total
$
$
869.6 $
21.6
60.1
91.1
1,734.4
1.5
1,676.7
4,455.0 $
192.0 $
3.5
45.5
6.7
194.5
1.5
376.7
820.4 $
677.6
18.1
14.6
84.4
1,539.9
—
1,300.0
3,634.6
(a) Contingent future licensing payments will be made if certain events take place, such as the launch of a specific test, the
transfer of certain technology, and the achievement of specified revenue milestones.
(b) The table does not include obligations under the Company’s pension and postretirement benefit plans, which are included
in Note 17 Pension and Postretirement Plans to Consolidated Financial Statements. Benefits under the Company's
postretirement medical plan are paid when claims are submitted for payment, the timing of which is not practicable to
estimate.
(c) The table does not include the Company’s reserve for unrecognized tax benefits. The Company had a $57.1 and $37.2
reserve for unrecognized tax benefits, including interest and penalties, at December 31, 2020, and 2019, respectively,
which is included in Note 14 Income Taxes to Consolidated Financial Statements.
(d) Interest payments due by period for the Company's debt subject to variable interest rates are calculated based on rates in
place as of December 31, 2020.
(e) Excludes amount of debt issuance costs included in the long-term debt balance.
Off-Balance Sheet Arrangements
The Company does not have transactions or relationships with “special purpose” entities, and the Company does not have
any off-balance sheet financing other than normal operating leases and letters of credit.
Other Commercial Commitments
As of December 31, 2020, the Company provided letters of credit aggregating approximately $77.4, primarily in connection
with certain insurance program which are renewed annually.
The contractual value of the noncontrolling interest put in the Company's Ontario subsidiary totaled $16.2 and $15.8 at
December 31, 2020, and 2019, respectively, and has been classified as mezzanine equity in the Company's consolidated balance
sheet.
Based on current and projected levels of cash flows from operations, coupled with availability under its revolving credit
facility, the Company believes it has sufficient liquidity to meet both its anticipated short-term and long-term cash needs;
however, the Company continually reassesses its liquidity position in light of market conditions and other relevant factors.
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Index
Critical Accounting Policies
The preparation of financial statements in conformity with generally accepted accounting principles requires management
to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets
and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reported
periods. While the Company believes these estimates are reasonable and consistent, they are by their very nature estimates of
amounts that will depend on future events. Accordingly, actual results could differ from these estimates. The Company’s Audit
Committee periodically reviews the Company’s significant accounting policies. The Company’s critical accounting policies
arise in conjunction with the following:
•
•
•
•
•
•
Revenue recognition;
Business combinations;
Pension expense;
Accruals for self-insurance reserves;
Income taxes; and
Goodwill and indefinite-lived assets.
Revenue Recognition
Dx
Within the Dx segment, a revenue transaction is initiated when Dx receives a requisition order to perform a diagnostic test.
The information provided on the requisition form is used to determine the party that will be billed for the testing performed and
the expected reimbursement. Dx recognizes revenue and satisfies its performance obligation for services rendered when the
testing process is complete and the associated results are reported. Revenues are distributed among four payer portfolios -
clients, patients, Medicare and Medicaid and third-party. Dx considers negotiated discounts and anticipated adjustments,
including historical collection experience for the payer portfolio, when sales are recorded.
The following are descriptions of the Dx payer portfolios:
Clients
Client payers represent the portion of Dx’s revenue related to physicians, hospitals, health systems, accountable care
organizations (ACOs), employers and other entities where payment is received exclusively from the entity ordering the testing
service. Generally, client revenues are recorded on a fee-for-service basis at Dx’s client list price, less any negotiated discount.
A portion of client billing is for laboratory management services, collection kits and other non-testing services or products. In
these cases, revenue is recognized when services are rendered or delivered.
Patients
This portfolio includes revenue from uninsured patients and member cost-share for insured patients (e.g., coinsurance,
deductibles and non-covered services). Uninsured patients are billed based upon Dx’s patient fee schedules, net of any
discounts negotiated with physicians on behalf of their patients. Dx bills insured patients as directed by their health plan and
after consideration of the fees and terms associated with an established health plan contract.
Medicare and Medicaid
This portfolio relates to fee-for-service revenue from traditional Medicare and Medicaid programs. Net revenue from these
programs is based on the fee schedule established by the related government authority. In addition to contractual discounts,
other adjustments including anticipated payer denials are considered when determining net revenue. Any remaining adjustments
to revenue are recorded at the time of final collection and settlement. These adjustments are not material to Dx’s results of
operations in any period presented.
Third-Party
Third-party includes revenue related to MCOs. The majority of Dx's third-party revenue is reimbursed on a fee-for-service
basis. These payers are billed at Dx's established list price and revenue is recorded net of contractual discounts. The majority of
Dx’s MCO revenues are recorded based upon contractually negotiated fee schedules with revenues for non-contracted MCOs
recorded based on historical reimbursement experience.
Third-party reimbursement is also received through capitation agreements with MCOs and independent physician
associations (IPAs). Under capitated agreements, revenue is recognized based on a negotiated per-member, per-month payment
for an agreed upon menu of tests, or based upon the proportionate share earned by Dx from a capitation pool. When the agreed
upon reimbursement is based solely on an established rate per member, revenue is not impacted by the volume of testing
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performed. Under a capitation pool arrangement, the aggregate value of an established rate per member is distributed based on
the volume and complexity of the procedures performed by laboratories participating in the agreement. Dx recognizes revenue
monthly, based upon the established capitation rate or anticipated distribution from a capitated pool.
Dx has a formal process to estimate implicit price concessions for uncollectable accounts. The majority of Dx's collection
risk is related to accounts receivable from both insured and uninsured patients who are unwilling or unable to pay. Anticipated
write-offs are recorded as adjustments to revenue at an amount considered necessary to record the segment's revenue at its net
realizable value. In addition to contractual discounts, other adjustments including anticipated payer denials and other external
factors that could affect the collectability of its receivables are considered when determining revenue and the net receivable
amount. Any remaining adjustments to revenue are recorded at the time of final collection and settlement. These adjustments
are not material to Dx's results of operations in any period presented.
DD
The nature of DD’s obligations includes agreements to provide preclinical services, to manage a full clinical trial, provide
services for a specific phase of a trial, or provide research products to the customer. Generally, the amount of the transaction
price estimated at the beginning of the contract is equal to the amount expected to be billed to the customer. Other payments
may also factor into the calculation of transaction price, such as volume-based rebates that are retroactively applied to prior
transactions in the period.
Historically a majority of DD's revenues have been earned under contracts that range in duration from a few months to a
few years, but can extend in duration up to five years or longer. Occasionally, DD also has entered into minimum volume
arrangements with certain customers. Under these types of arrangements, if the annual minimum dollar value of a service
commitment is not reached, the customer is required to pay DD for the shortfall. Annual minimum commitment shortfalls are
not recognized until the end of the period when the amount has been determined and agreed to by the customer.
DD recognizes revenue either as services are performed or as products are delivered, depending on the nature of the work
contracted. If performance is completed at a specific point in time, the Company evaluates the nature of the agreement to
determine when the good or service is transferred into the customer’s control.
Service contracts generally take the form of fee-for-service or fixed-price arrangements subject to pricing adjustments based
on changes in scope. In cases where performance spans multiple accounting periods, revenue is recognized as services are
performed, measured on a proportional-performance basis, using either input or output methods that are specific to the service
provided. In an output method, revenue is determined by dividing the actual units of output achieved by the total units of output
required under the contract and multiplying that percentage by the total contract value. The total contract value, or total
contractual payments, represents the aggregate contracted price for each of the agreed upon services to be provided. When
using an input method, revenue is recognized by dividing the actual units of input incurred by the total units of input budgeted
in the contract, and multiplying that percentage by the total contract value. In each situation, the Company believes that the
methods used most accurately depict the progress of the Company towards completing its obligations.
Billing schedules and payment terms are generally negotiated on a contract-by-contract basis. In some cases, DD bills the
customer for the total contract value in progress-based installments as certain non-contingent billing milestones are reached
over the contract duration. These milestones include, but are not limited to, contract signing, initial dosing, investigator site
initiation, patient enrollment and/or database lock. The term “billing milestone” relates only to a billing trigger in a contract
whereby amounts become billable and payable in accordance with a negotiated predetermined billing schedule throughout the
term of a project. These billing milestones are generally not performance-based (i.e., there is no potential additional
consideration tied to specific deliverables or performance). In other cases, billing and payment terms are tied to the passage of
time (e.g., monthly billings). In either case, the total contract value and aggregate amounts billed to the customer would be the
same at the end of the project.
Proportional performance contracts typically contain a single service (e.g., management of a clinical study) and therefore no
allocation of the contract price is required. Fee-for-service contracts are typically priced based on transaction volume. Since the
volume of activities in a fee-for-service contract is unspecified, the contract price is entirely variable and is allocated to the time
period in which it is earned. For contracts that include multiple distinct goods and services, DD allocates the contract price to
the goods and services based on a customer price list, if available. If a price list is not available, DD will estimate the
transaction price using either market prices or an “expected cost plus margin” approach.
While DD attempts to negotiate terms that provide for billing and payment of services prior or within close proximity to the
provision of services, this is not always possible. While a project is ongoing, cash payments are not necessarily representative
of aggregate revenue earned at any particular point in time, as revenues are recognized when services are provided, while
amounts billed and paid are in accordance with the negotiated billing and payment terms.
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In some cases, payments received are in excess of revenue recognized. For example, a contract invoicing schedule may
provide for an upfront payment of 10% of the full contract value upon contract signing, but at the time of signing performance
of services has not yet begun. Payments received in advance of services being provided are deferred as contract liabilities on the
balance sheet. As the contracted services are subsequently performed and the associated revenue is recognized, the contract
liability balance is reduced by the amount of revenue recognized during the period.
In other cases, services may be provided and revenue recognized before the customer is invoiced. In these cases, revenue
recognized will exceed amounts billed, and the difference, representing a contract asset, is recorded for the amount that is
currently not billable to the customer pursuant to contractual terms. Once the customer is invoiced, the contract asset is reduced
for the amount billed, and a corresponding account receivable is recorded. All contract assets are billable to customers within
one year from the respective balance sheet date.
Most contracts are terminable with or without cause by the customer, either immediately or upon notice. These contracts
often require payment to DD of expenses to wind down the study or project, fees earned to date and, in some cases, a
termination fee or a payment to DD of some portion of the fees or profits that could have been earned by DD under the contract
if it had not been terminated early. Termination fees are included in revenues when services are performed and realization is
assured.
The following are descriptions of the revenue recognition models of the drug development services provided by DD:
Preclinical services include fee-for-service activities such as bioanalytical testing services, and proportional performance
activities such as toxicology studies. Revenue for sale of research models is recognized at a point in time, typically upon
shipment, when control transferred to the customer. Revenue for bioanalytical testing services is recognized at a point in time
upon communication of results to the customer. Revenue for proportional performance activities, including toxicology studies,
is recognized using an input-based measure of progress in which revenue is recognized as expenses are incurred for the research
models, labor hours, and other costs attributable to the study.
Through its central laboratory, DD produces and supplies specimen collection kits that are utilized in clinical studies, and
provides transportation, project management, data management, and laboratory testing services on an as-needed basis
throughout the duration of its customers’ clinical studies. Revenue for central laboratory services is recognized using an output-
based measure of progress based on volume of activities in each period. DD also provides long-term specimen storage services,
for which revenue is recognized using an input-based measure of progress based on costs incurred.
DD provides clinical development and commercialization services, including clinical pharmacology services, full
management of Phase II through IV clinical studies, and market access solutions. Revenue for clinical pharmacology services,
which includes first-in-human trials, is recognized using an output-based measure of progress based on bed nights. The majority
of clinical development and commercialization service long-term contracts are service contracts for clinical research that
represent a single performance obligation (e.g., management of a clinical study). Revenue for these service contracts is
recognized over time based on the progress of the performance obligation which is measured by the proportion of the actual
costs incurred to the total costs expected to complete the contract (including labor and pass-through costs such as investigator
grants and reimbursable out-of-pocket expenses). This cost-based method of revenue recognition requires management to
estimate the costs to complete these services on an ongoing basis. Clinical services utilizing the input-based measure of
progress account for approximately 50% of DD revenue. Revenue for market access solutions is recognized using various
methods. Revenue for fee-for-service arrangements, such as reimbursement consulting hotlines and patient assistance programs,
is recognized using an output method based on transaction volume which corresponds to the amount charged to the customer.
For consulting services billed based on time and materials, revenue is recognized using the right to invoice practical expedient.
DD endeavors to assess and monitor the creditworthiness of its customers to which it grants credit terms in the ordinary
course of business. DD maintains a provision for doubtful accounts relating to amounts due that may not be collected. This bad
debt provision is monitored on a monthly basis and adjusted as circumstances warrant. Since the recorded bad debt provision is
based upon management's judgment, actual bad debt write-offs may be greater or less than the amount recorded. Historically,
bad debt write-offs have not been material.
Business Combinations
The Company accounts for business combination transactions under the acquisition method of accounting and reported the
results of operations of the acquired entities from its respective date of acquisition. Assets acquired were recorded at their
estimated fair values as of the acquisition date. Estimated fair values were based on various valuation methodologies, including
an income approach using primarily discounted cash flow techniques for the customer relationships intangible assets. The
aforementioned income methods utilize management's estimates of future operating results and cash flows discounted using a
weighted-average cost of capital that reflects market participant assumptions. The excess of the fair value of the consideration
conveyed over the fair value of the assets acquired was recorded as goodwill. The goodwill reflects management's expectations
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of the ability to gain access to and penetrate the acquired entities' historical patient base and the benefits of being able to
leverage operational efficiencies with favorable growth opportunities based on positive demographic trends in the market. None
of the goodwill recorded as a result of the current year transactions is deductible for federal income tax purposes.
As described in Note 3 Business Acquisitions and Dispositions to the consolidated financial statements, the Company
acquired various businesses and related assets for approximately $267.6 in cash (net of cash acquired). The purchase
consideration for all acquisitions has been allocated to the estimated fair market value of the net assets acquired, including
approximately $121.3 in identifiable intangible assets and a residual amount of non-tax-deductible goodwill of approximately
$166.2. The amortization periods for intangible assets acquired from these businesses range from 12 to 15 years for customer
relationships. These acquisitions were made primarily to extend the Company's geographic reach in important market areas,
enhance the Company's scientific differentiation and to expand the breadth and scope of the Company's CRO services. The
excess of the fair value of the consideration conveyed over the fair value of the net assets acquired was recorded as
goodwill. The goodwill reflects the Company's expectations to utilize the acquired businesses’ workforce and established
relationships and the benefits of being able to leverage operational efficiencies with favorable growth opportunities in these
markets.
Pension Expense
The Company sponsors both funded and unfunded defined benefit pension plans which provide benefits based on various
criteria such as years of service and salary. The Company maintained two plans in the United States, three plans in the United
Kingdom and one in Germany.
The two plans in the United States (U.S. Plans) were closed to new entrants and the accrual of service credits at the end of
2009. The U.K. pension plans were closed to new entrants and the accrual of service credits for one plan as of December 31,
2002 and the accrual of service credits for the other two plans as of December 31, 2019. The German plan is closed to new
entrants but participants continue to accrue service credits. The U.K. and German plans are aggregated for disclosure as the
Non-U.S. Plans.
The Company's net pension cost is developed from actuarial valuations. Inherent in these valuations are key assumptions,
including discount rates and expected return on plan assets, which are updated on an annual basis at the beginning of each year.
The Company is required to consider current market conditions, including changes in interest rates, in making these
assumptions. Changes in pension costs may occur in the future due to changes in these assumptions. The key assumptions used
in accounting for the defined-benefit retirement plans are summarized below:
Weighted average assumptions used to determine net periodic benefit costs are as follows:
Discount rate
Salary increases
Expected long term rate of return
Cash balance interest credit rate
U. S. Plans
Non-U.S. Plans
Year ended December 31, 2020
3.3 %
N/A
6.0 %
4.0 %
1.7 %
3.1 %
3.5
N/A
Weighted average assumptions used to determine net periodic benefit obligations are as follows:
Discount rate
Salary increases
Discount Rate
U. S. Plans
Non-U.S. Plans
Year Ended December 31, 2020
2.3 %
N/A
1.2 %
2.0 %
The Company evaluates several approaches toward setting the discount rate assumption that is used to value the benefit
obligations of its retirement plans. At year-end, priority was given to use of the Towers Watson Bond:Link model, which
simulates the purchase of investment-grade corporate bonds at current market yields with principal amounts and maturity dates
closely matching the Company's projected cash disbursements from its plans. This completed model represents the yields to
maturity at which the Company could theoretically settle its plan obligations at year end. The weighted-average yield on the
modeled bond portfolio is then used to form the discount rate assumption used for each retirement plan. A one percentage point
decrease or increase in the discount rate would have resulted in a respective increase or decrease in 2020 retirement plan
expense of $1.9 for the U.S Plans. A one percentage point decrease or increase in the discount rate would have resulted in a
respective increase or decrease in 2020 retirement plan expense of $2.1 for the Non-U.S. Plans.
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Return on Plan Assets
In establishing its expected return on plan assets assumption, the Company reviews its asset allocation and develops return
assumptions based on different asset classes, adjusting for plan operating expenses. Actual asset over/under performance
compared to expected returns will respectively decrease/increase unrecognized loss. The change in the unrecognized loss will
change amortization cost in upcoming periods. A one percentage point increase or decrease in the expected return on plan assets
would have resulted in a corresponding change in 2020 pension expense of $2.5 for the U.S. Plans. A one percentage point
increase or decrease in the expected return on plan assets would have resulted in a corresponding change in 2020 pension
expense of $4.8 for the Non-U.S. Plans.
Net pension cost for 2020 was $11.0 as compared with $13.8 in 2019. The decrease in pension expense was due to market
performance partially offset by lower discount rates. Pension expense for the U.S. Plans is expected to decrease to $6.5 in 2021
primarily due to the impact of strong asset returns in 2020, and the $30.0 contribution made in December 2020, offset by lower
discount rates in certain plans. Pension expense for the Non-U.S. Plans is expected to decrease by approximately $0.2 in 2021,
primarily due to lower service cost partially offset by a lower discount rate in 2021.
Further information on the Company’s defined-benefit retirement plans is provided in Note 17 Pension and Postretirement
Plans to the Consolidated Financial Statements.
Accruals for Self-Insurance Reserves
Accruals for self-insurance reserves (including workers’ compensation, auto and employee medical) are determined based
on a number of assumptions and factors, including historical payment trends and claims history, actuarial assumptions and
current and estimated future economic conditions. These estimated liabilities are not discounted.
The Company is self-insured (up to certain limits) for professional liability claims arising in the normal course of business,
generally related to the testing and reporting of laboratory test results. The Company maintains excess insurance which limits
the Company’s maximum exposure on individual claims. The Company estimates a liability that represents the ultimate
exposure for aggregate losses below those limits. The liability is based on assumptions and factors for known and incurred but
not reported claims, including the frequency and payment trends of historical claims.
If actual trends differ from these estimates, the financial results could be impacted. Historical trends have not differed
significantly from these estimates.
Income Taxes
The Company accounts for income taxes utilizing the asset and liability method. Under this method, deferred tax assets and
liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying
amounts of existing assets and liabilities and their respective tax bases and for tax loss carryforwards. Deferred tax assets and
liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary
differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is
recognized in income in the period that includes the enactment date. The Company does not recognize a tax benefit, unless the
Company concludes that it is more likely than not that the benefit will be sustained on audit by the taxing authority based solely
on the technical merits of the associated tax position. If the recognition threshold is met, the Company recognizes a tax benefit
measured at the largest amount of the tax benefit that the Company believes is greater than 50% likely to be realized. The
Company records interest and penalties in income tax expense.
Goodwill and Indefinite-Lived Assets
The Company assesses goodwill and indefinite-lived intangibles for impairment at least annually or whenever events or
changes in circumstances indicate that the carrying amount of such assets may not be recoverable. In accordance with updates
to the Financial Accounting Standards Board's (FASB) authoritative guidance regarding goodwill and indefinite-lived
intangible asset impairment testing, an entity is allowed to first assess qualitative factors as a basis for determining whether it is
necessary to perform quantitative impairment testing. If an entity determines that it is not more likely than not that the estimated
fair value of an asset is less than its carrying value, then no further testing is required. Otherwise, impairment testing must be
performed in accordance with the original accounting standards. The updated FASB guidance also allows an entity to bypass
the qualitative assessment for any reporting unit in its goodwill assessment and proceed directly to performing the quantitative
assessment. Similarly, a company can proceed directly to a quantitative assessment in the case of impairment testing for
indefinite-lived intangible assets as well.
The quantitative goodwill impairment test includes the estimation of the fair value of each reporting unit as compared to
the carrying value of the reporting unit. Reporting units are businesses with discrete financial information that is available and
reviewed by management. The Company estimates the fair value of a reporting unit using both income-based and market-based
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valuation methods. The income-based approach is based on the reporting unit's forecasted future cash flows that are discounted
to the present value using the reporting unit's weighted average cost of capital. For the market-based approach, the Company
utilizes a number of factors such as publicly available information regarding the market capitalization of the Company as well
as operating results, business plans, market multiples, and present value techniques. Based upon the range of estimated values
developed from the income and market-based methods, the Company determines the estimated fair value for the reporting unit.
If the estimated fair value of the reporting unit exceeds the carrying value, the goodwill is not impaired, and no further review is
required. An entity should recognize an impairment charge for the amount by which the carrying amount exceeds the reporting
unit’s fair value; however, the loss recognized should not exceed the total amount of goodwill allocated to that reporting unit.
The income-based fair value methodology requires management's assumptions and judgments regarding economic
conditions in the markets in which the Company operates and conditions in the capital markets, many of which are outside of
management's control. At the reporting unit level, fair value estimation requires management's assumptions and judgments
regarding the effects of overall economic conditions on the specific reporting unit, along with assessment of the reporting unit's
strategies and forecasts of future cash flows. Forecasts of individual reporting unit cash flows involve management's estimates
and assumptions regarding:
•
•
•
Annual cash flows, on a debt-free basis, arising from future revenues and profitability, changes in working capital, capital
spending and income taxes for at least a five-year forecast period.
A terminal growth rate for years beyond the forecast period. The terminal growth rate is selected based on consideration of
growth rates used in the forecast period, historical performance of the reporting unit and economic conditions.
A discount rate that reflects the risks inherent in realizing the forecasted cash flows. A discount rate considers the risk-free
rate of return on long-term treasury securities, the risk premium associated with investing in equity securities of
comparable companies, the beta obtained from the comparable companies and the cost of debt for investment grade issuers.
In addition, the discount rate may consider any company-specific risk in achieving the prospective financial information.
Under the market-based fair value methodology, judgment is required in evaluating market multiples and recent
transactions. Management believes that the assumptions used for its impairment tests are representative of those that would be
used by market participants performing similar valuations of the reporting units.
The Company assesses goodwill and indefinite-lived intangibles for impairment at least annually or whenever events or
changes in circumstances indicate that the carrying amount of such assets may not be recoverable. Based upon the revised
forecasted revenues and operating income following the declaration of the COVID-19 global pandemic, management concluded
there was a triggering event and updated its annual 2019 goodwill impairment testing as of March 31, 2020, for certain of its
DD and Dx reporting units. Based on the quantitative impairment assessment performed in the same manner as the Company's
annual quantitative assessment, the Company concluded that the fair value was less than carrying value for two of its reporting
units, including one where the 2019 fair value exceeded carrying value by approximately 10.0%, and recorded a goodwill
impairment of $418.7 for the DD segment and $3.7 for the Dx segment.
Management performed its annual goodwill and intangible asset impairment testing as of the beginning of the fourth
quarter of 2020. The Company elected to perform the qualitative assessment for goodwill and intangible assets for the domestic
Dx reporting units and certain DD reporting units, a quantitative assessment for two of the DD reporting units, and a
quantitative assessment for the Canadian reporting unit and its indefinite-lived assets consisting of acquired Canadian licenses.
In the qualitative assessment, the Company considered relevant events and circumstances for each reporting unit, including
(i) current year results, (ii) financial performance versus management’s annual and five-year strategic plans, (iii) changes in the
reporting unit carrying value since prior year, (iv) industry and market conditions in which the reporting unit operates, (v)
macroeconomic conditions, including discount rate changes, and (vi) changes in products or services offered by the reporting
unit. If applicable, performance in recent years was compared to forecasts included in prior valuations. Based on the results of
the qualitative assessment, the Company concluded that it was not more likely than not that the carrying values of the goodwill
and intangible assets were greater than their fair values, and that further quantitative testing was not necessary.
In 2020, the Company utilized a combination of the market and income approaches to determine the fair value of the DD
reporting units and the income approach to determine the fair value of the Canadian reporting unit and its indefinite-lived assets
consisting of acquired Canadian licenses. Based upon the results of the quantitative assessments, the Company concluded that
the fair values of the goodwill and intangible assets, including the indefinite-lived Canadian licenses, was greater than the
carrying value.
It is possible that the Company's conclusions regarding impairment or recoverability of goodwill or intangible assets in any
reporting unit could change in future periods. There can be no assurance that the estimates and assumptions used in the
Company's goodwill and intangible asset impairment testing performed as of the beginning of the fourth quarter of 2020 will
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prove to be accurate predictions of the future, if, for example, (i) the businesses do not perform as projected, (ii) overall
economic conditions in 2020 or future years vary from current assumptions (including changes in discount rates), (iii) business
conditions or strategies for a specific reporting unit change from current assumptions, including loss of major customers, (iv)
investors require higher rates of return on equity investments in the marketplace or (v) enterprise values of comparable publicly
traded companies, or actual sales transactions of comparable companies, were to decline, resulting in lower multiples of
revenues and EBITDA. Management's impairment analysis for certain reporting units utilized significant judgments and
assumptions related to the market comparable method analysis, such as selected market multiples, and related to cash flow
projections, such as revenue and terminal growth rate, projected operating income, and the discount rate. A significant increase
in the discount rate, decrease in the revenue and terminal growth rate, decreased operation margin or substantial reductions in
end markets and volume assumptions could have a negative impact on the estimated fair value of certain reporting units. A
future impairment charge for goodwill or intangible assets could have a material effect on the Company's consolidated financial
position and results of operations.
Item 7A.
QUANTITATIVE AND QUALITATIVE DISCLOSURE ABOUT MARKET RISK (in millions)
Market risk is the potential loss arising from adverse changes in market rates and prices, such as foreign currency exchange
rates, interest rates and other relevant market rate or price changes. In the ordinary course of business, the Company is exposed
to various market risks, including changes in foreign currency exchange and interest rates, and the Company regularly evaluates
the exposure to such changes. The Company addresses its exposure to market risks, principally the market risks associated with
changes in foreign currency exchange rates and interest rates, through a controlled program of risk management that includes,
from time to time, the use of derivative financial instruments such as foreign currency forward contracts, cross currency swaps
and interest rate swap agreements. Although, as set forth below, the Company’s zero-coupon subordinated notes contained
features that were considered to be embedded derivative instruments, the Company does not hold or issue derivative financial
instruments for trading purposes.
Foreign Currency Exchange Rates
Approximately 10.7% and 12.7% of the Company's revenues for the year ended December 31, 2020 and 2019, respectively,
were denominated in currencies other than the U.S. dollar (USD). The Company's financial statements are reported in USD and,
accordingly, fluctuations in exchange rates will affect the translation of revenues and expenses denominated in foreign
currencies into USD for purposes of reporting the Company's consolidated financial results. In both 2020 and 2019, the most
significant currency exchange rate exposures were to the Canadian dollar, Swiss franc, euro and British pound. Excluding the
impacts from any outstanding or future hedging transactions, a hypothetical change of 10% in average exchange rates used to
translate all foreign currencies to USD would have impacted income before income taxes for 2020 by approximately $9.1.
Gross accumulated currency translation adjustments recorded as a separate component of shareholders’ equity were $264.1 and
$104.4 at December 31, 2020, and 2019, respectively. The Company does not have significant operations in countries in which
the economy is considered to be highly inflationary.
The Company earns revenue from service contracts over a period of several months and, in some cases, over a period of
several years. Accordingly, exchange rate fluctuations during this period may affect the Company's profitability with respect to
such contracts. The Company is also subject to foreign currency transaction risk for fluctuations in exchange rates during the
period of time between the consummation and cash settlement of transactions. The Company limits its foreign currency
transaction risk through exchange rate fluctuation provisions stated in some of its contracts with customers, or it may hedge
transaction risk with foreign currency forward contracts. At December 31, 2020, the Company had 31 open foreign exchange
forward contracts with various amounts maturing monthly through January 2021 with a notional value totaling approximately
$601.2. At December 31, 2019, the Company had 34 open foreign exchange forward contracts with various amounts maturing
monthly through January 2020 with a notional value totaling approximately $369.2.
The Company is party to USD to Swiss Franc cross-currency swap agreements with a notional amount of $600.0, maturing
in 2022 and 2025, as a hedge against the impact of foreign exchange movements on its net investment in its Swiss Franc
functional currency subsidiary.
Interest Rates
Some of the Company's debt is subject to interest at variable rates. As a result, fluctuations in interest rates affect the
Company's financial results. The Company attempts to manage interest rate risk and overall borrowing costs through an
appropriate mix of fixed and variable rate debt including the utilization of derivative financial instruments, primarily interest
rate swaps.
Borrowings under the Company's term loan credit facilities and revolving credit facility are subject to variable interest rates,
unless fixed through interest rate swaps or other agreements. As of December 31, 2020, and 2019, the Company had
approximately $375.0 and $375.0, respectively, of unhedged variable rate debt under the 2019 term loan credit facility.
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Each quarter-point increase or decrease in the variable rate would result in the Company's interest expense changing by
approximately $0.9 per year for the Company's unhedged variable rate debt.
During the third quarter of 2013, the Company entered into two fixed-to-variable interest rate swap agreements for its
4.625% Senior Notes due 2020 with an aggregate notional amount of $600.0 and variable interest rates based on one-month
London Interbank Offered Rate (LIBOR) plus 2.298% to hedge against changes in the fair value of a portion of the Company's
long-term debt. The Company exited one of these swap arrangements in December 2019 in connection with the redemption of
$187.9 of the 4.625% Senior Notes due 2020 and recorded a gain of $1.6. The Company exited the remaining fixed-to-variable
interest rate swap agreement in August 2020, in connection with the redemption of the remaining $412.2 of its 4.625% Senior
Notes due November 15, 2020, and recorded a gain of $1.6 on the extinguishment.
On December 19, 2019, the Company redeemed any remaining outstanding zero-coupon subordinated notes due 2021 (the
zero-coupon notes) that had not previously converted.
Item 8.
FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA
The consolidated financial statements of the Company required in this item are set forth beginning on page F-1 of this Annual
Report on Form 10-K.
Item 9.
None.
CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND
FINANCIAL DISCLOSURE
Item 9A.
CONTROLS AND PROCEDURES
Disclosure Controls and Procedures
As of the end of the period covered by this Annual Report, the Company carried out under the supervision and with the
participation of the Company’s management, including the Company’s principal executive officer and principal financial
officer, an evaluation of the effectiveness of the Company's disclosure controls and procedures (as defined in Rules 13a-15(e)
and 15d-15(e) under the Securities Exchange Act of 1934, as amended). Based upon this evaluation, the Company’s principal
executive officer and principal financial officer concluded that the Company’s disclosure controls and procedures were
effective as of the end of the period covered by this Annual Report.
Changes in Internal Control over Financial Reporting
There have been no changes in the Company’s internal control over financial reporting (as defined in Exchange Act Rules
13a-15(f) and 15d-15(f)) during the quarter ended December 31, 2020, that have materially affected, or are reasonably likely to
materially affect, the Company’s internal control over financial reporting.
Report of Management on Internal Control over Financial Reporting
The Company's management is responsible for establishing and maintaining adequate internal control over financial
reporting (as defined in Rules 13a-15(f) and 15d-15(f) under the Securities Exchange Act of 1934).
The internal control over financial reporting at the Company was designed to provide reasonable assurance regarding the
reliability of financial reporting and the preparation of financial statements for external purposes in accordance with accounting
principles generally accepted in the U.S. Internal control over financial reporting includes those policies and procedures that:
•
•
•
•
pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and
dispositions of the assets of the Company;
provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements
in accordance with accounting principles generally accepted in the U.S.;
provide reasonable assurance that receipts and expenditures of the Company are being made only in accordance with
authorization of management and directors of the Company; and
provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition
of assets that could have a material effect on the consolidated financial statements.
Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements.
The Company's management assessed the effectiveness of the Company’s internal control over financial reporting as of
December 31, 2020. Management based this assessment on criteria for effective internal control over financial reporting
described in “Internal Control - Integrated Framework 2013” issued by the Committee of Sponsoring Organizations of the
63
Index
Treadway Commission (COSO). Based on this assessment, the Company's management determined that, as of December 31,
2020, the Company maintained effective internal control over financial reporting. Management reviewed the results of its
assessment with the Audit Committee of the Company’s board of directors.
PricewaterhouseCoopers LLP, an independent registered public accounting firm, who audited and reported on the
consolidated financial statements of the Company included in this Annual Report, also audited the effectiveness of the
Company’s internal control over financial reporting as of December 31, 2020, as stated in its report, which is included herein
immediately preceding the Company’s audited financial statements.
Item 9B.
OTHER INFORMATION
None.
PART III
Item 10.
DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE
The information required by the item regarding directors is incorporated by reference to the Company’s Definitive Proxy
Statement to be filed with the Securities and Exchange Commission in connection with the Annual Meeting of Stockholders to
be held in 2021 (the 2021 Proxy Statement) under the caption Election of Directors. Information regarding executive officers is
incorporated by reference to the Company’s 2021 Proxy Statement under the caption Executive Officers. Information
concerning the Company’s Audit Committee, including the designation of audit committee financial experts and information
regarding compliance with Section 16(a) of the Exchange Act responsive to this item is incorporated by reference to the
Company’s 2021 Proxy Statement under the captions Corporate Governance and Delinquent Section 16(a) Reports,
respectively. Information concerning the Company's code of ethics is incorporated by reference to the Company's 2021 Proxy
Statement under the caption Corporate Governance Policies and Procedures.
Item 11.
EXECUTIVE COMPENSATION
The information required by this item is incorporated by reference to information in the 2021 Proxy Statement under the
captions “Executive Compensation” and “Director Compensation.”
Item 12.
SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND
RELATED STOCKHOLDER MATTERS
See Note 15 Stock Compensation Plans to the Consolidated Financial Statements for a discussion of the Company’s Stock
Compensation Plans. Except for the above referenced footnote, the information called for by this item is incorporated by
reference to information in the 2021 Proxy Statement under the captions “Security Ownership of Certain Beneficial Holders
and Management,” “Compensation Discussion and Analysis” and “Executive Compensation.”
Item 13.
CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR
INDEPENDENCE
The information required by this item is incorporated by reference to information in the 2021 Proxy Statement under the
captions “Board Independence” and “Related Party Transactions.”
Item 14.
PRINCIPAL ACCOUNTANT FEES AND SERVICES
The information required by this item is incorporated by reference to information in the 2021 Proxy Statement under the
caption “Fees to Independent Registered Public Accounting Firm.”
64
Index
Item 15.
EXHIBITS AND FINANCIAL STATEMENT SCHEDULES
(a) List of documents filed as part of this Annual Report:
PART IV
Consolidated Financial Statements and Report of Independent Registered Public Accounting Firm
included herein:
(1)
See Index on page F-1
(2)
Financial Statement Schedules:
All schedules are omitted as they are inapplicable or the required information is furnished in the
Consolidated Financial Statements or notes thereto.
(3)
Index to and List of Exhibits
3.1
3.2
4.1
4.2
4.3
4.4
4.5
4.6
4.7
4.8
4.9
4.10
4.11
4.12
Amended and Restated Certificate of Incorporation of the Company dated May 24, 2001 (incorporated herein by
reference to Exhibit 3.1 to the Company’s Registration Statement on Form S-3, filed with the Commission on
October 19, 2001, File No. 333-71896).
Amended and Restated By-Laws of the Company, adopted and effective July 7, 2020 (incorporated by reference
herein to Exhibit 3.1 to the Company’s Quarterly Report on Form 10-Q for the period ended June 30, 2020. and
Restated By-Laws of the Company.
Specimen of the Company’s Common Stock Certificate (incorporated herein by reference to Exhibit 4.1 to the
Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2001).
Indenture, dated as of November 19, 2010, between the Company and U.S. Bank National Association, as trustee
(incorporated herein by reference to Exhibit 4.1 to the Company’s Current Report on Form 8-K filed on
November 19, 2010).
Second Supplemental Indenture, dated as of November 19, 2010, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2020 Notes (incorporated herein by reference to Exhibit 4.3 to
the Company’s Current Report on Form 8-K filed on November 19, 2010).
Third Supplemental Indenture, dated as of August 23, 2012, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2017 Notes (incorporated herein by reference to Exhibit 4.2 to
the Company’s Current Report on Form 8-K filed on August 23, 2012).
Fourth Supplemental Indenture, dated as of August 23, 2012, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2022 Notes (incorporated herein by reference to Exhibit 4.3 to
the Company’s Current Report on Form 8-K filed on August 23, 2012).
Fifth Supplemental Indenture, dated as of November 1, 2013, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2018 Notes (incorporated herein by reference to Exhibit 4.2 to
the Company’s Current Report on Form 8-K filed on November 1, 2013).
Sixth Supplemental Indenture, dated as of November 1, 2013, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2023 Notes (incorporated herein by reference to Exhibit 4.3 to
the Company’s Current Report on Form 8-K filed on November 1, 2013).
Seventh Supplemental Indenture, dated as of January 30, 2015, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2020 Notes (incorporated herein by reference to Exhibit 4.2 to
the Company’s Current Report on Form 8-K filed on January 30, 2015).
Eighth Supplemental Indenture, dated as of January 30, 2015, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2022 Notes (incorporated herein by reference to Exhibit 4.3 to
the Company’s Current Report on Form 8-K filed on January 30, 2015).
Ninth Supplemental Indenture, dated as of January 30, 2015, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2025 Notes (incorporated herein by reference to Exhibit 4.4 to
the Company’s Current Report on Form 8-K filed on January 30, 2015).
Tenth Supplemental Indenture, dated as of January 30, 2015, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2045 Notes (incorporated herein by reference to Exhibit 4.5 to
the Company’s Current Report on Form 8-K filed on January 30, 2015).
Eleventh Supplemental Indenture, dated as of August 22, 2017, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2024 Notes (incorporated by reference to Exhibit 4.2 to the
Company’s Current Report on Form 8-K filed on August 22, 2017).
65
Index
4.13
4.14
4.15
4.16*
10.1+
10.2+
10.3+
10.4+
10.5+
10.6+
10.7+
10.8+
10.9+
10.10+
10.11+
10.12+
10.13+
10.14
Twelfth Supplemental Indenture, dated as of August 22, 2017, between the Company and U.S. Bank National
Association, as trustee, including the form of the 2027 Notes (incorporated by reference to Exhibit 4.3 to the
Company’s Current Report on Form 8-K filed on August 22, 2017).
Thirteenth Supplemental Indenture, dated as of November 25, 2019, between the Company and U.S. Bank
National Association, as trustee, including the form of the 2024 Notes (incorporated herein by reference to
Exhibit 4.2 to the Company's Current Report on Form 8-K filed on November 25, 2019).
Fourteenth Supplemental Indenture, dated as of November 25, 2019, between the Company and U.S. Bank
National Association, as trustee, including the form of the 2029 Notes (incorporated herein by reference to
Exhibit 4.3 to the Company's Current Report on Form 8-K filed on November 25, 2019).
Description of the Registrant's securities registered pursuant to Section 12 of the Securities Exchange Act of
1934.
National Health Laboratories Incorporated Pension Equalization Plan (incorporated herein by reference to the
Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 1992).
Laboratory Corporation of America Holdings Amended and Restated New Pension Equalization Plan
(incorporated herein by reference to Exhibit 10.1 to the Company's Quarterly Report on Form 10-Q for the
period ended September 30, 2004).
First Amendment to the Laboratory Corporation of America Holdings Amended and Restated New Pension
Equalization Plan (incorporated herein by reference to Exhibit 10.2 to the Company’s Quarterly Report on Form
10-Q for the period ended September 30, 2004).
Second Amendment to the Laboratory Corporation of America Holdings Amended and Restated New Pension
Equalization Plan (incorporated herein by reference to Exhibit 10.4 to the Company’s Annual Report on Form
10-K for the fiscal year ended December 31, 2004).
Laboratory Corporation of America Holdings Deferred Compensation Plan (incorporated herein by reference to
Exhibit 10.22 the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2004).
First Amendment to the Laboratory Corporation of America Holdings Deferred Compensation Plan
(incorporated herein by reference to Exhibit 10.23 to the Company’s Annual Report on Form 10-K for the fiscal
year ended December 31, 2004).
Second Amendment to the Laboratory Corporation of America Holdings Deferred Compensation Plan
(incorporated herein by reference to Exhibit 10.8 to the Company’s Quarterly Report on Form 10-Q for the
period ended June 30, 2005).
Third Amendment to the Laboratory Corporation of America Amended and Restated New Pension Equalization
Plan (incorporated herein by reference Exhibit 10.6 to the Company’s Quarterly Report on Form 10-Q for the
period ended June 30, 2005).
Third Amendment to the Laboratory Corporation of America Holdings Deferred Compensation Plan
(incorporated herein by reference to Exhibit 10.28 to the Company’s Annual Report on Form 10-K for the fiscal
year ended December 31, 2006).
Fourth Amendment to the Laboratory Corporation of America Holdings Deferred Compensation Plan
(incorporated herein by reference to Exhibit 10.34 to the Company’s Annual Report on Form 10-K for the fiscal
year ended December 31, 2007).
Laboratory Corporation of America Holdings 2008 Stock Incentive Plan (incorporated herein by reference to
Annex III to the Company’s Definitive Proxy Statement on Schedule 14A filed on March 25, 2008).
Amendment to Laboratory Corporation of America Holdings 2008 Stock Incentive Plan (incorporated herein by
reference to Exhibit 10.2 to the Company’s Current Report on Form 8-K filed on May 7, 2008).
Laboratory Corporation of America Holdings 2012 Omnibus Incentive Plan (incorporated herein by reference to
Exhibit 10.1 to the Company’s Current Report on Form 8-K filed on May 2, 2012).
Second Amended and Restated Credit Agreement, dated as of September 15, 2017, (originally dated as of
December 21, 2011), among the Company, Bank of America, N.A. as Administrative Agent, Swing Line Lender
and L/C Issuer, Wells Fargo Bank, National Association as Syndication Agent and L/C Issuer, Credit Suisse AG,
Cayman Islands Branch as Documentation Agent and L/C Issuer, the Bank of Tokyo-Mitsubishi UFJ, LTD.,
Barclays Bank PLC, Credit Suisse AG, Cayman Islands Branch, KeyBank National Association, PNC Bank,
National Association, TD Bank, N.A., and U.S. Bank National Association, as Documentation Agents, Merrill
Lynch, Pierce, Fenner & Smith Incorporated, Wells Fargo Securities, LLC and Credit Suisse Securities (USA)
LL as Joint Lead Arrangers and Joint Book Managers, and the lenders named therein (incorporated herein by
reference to Exhibit 10.3 to the Company’s Annual Report on Form 10-Q filed on November 2, 2017).
66
Index
10.15
10.16+
10.17+
10.18
10.19
10.20+
10.21*+
16.1
21*
23.1*
24.1*
24.2*
24.3*
24.4*
24.5*
24.6*
24.7*
24.8*
31.1*
31.2*
32*
Amendment No. 1, dated as of May 7, 2020, to the Second Amended and Restated Credit Agreement, dated
September 15, 2017 (originally dated as of December 21, 2011), among the Company, Bank of America, N.A. as
administrative agent, and the lenders party thereto (incorporated herein by reference to Exhibit 10.2 to the
Company’s Quarterly Report on Form 10-Q filed on May 8, 2020).
Laboratory Corporation of America Holdings 2016 Omnibus Incentive Plan (incorporated by reference herein to
Exhibit 10.1 to the Company’s Current Report on Form 8-K filed on May 16, 2016).
Laboratory Corporation of America Holdings 2016 Employee Stock Purchase Plan (incorporated by reference
herein to Exhibit 10.2 to the Company’s Current Report on Form 8-K filed on May 16, 2016).
Term Loan Credit Agreement, dated June 3, 2019, by and among Laboratory Corporation of America Holdings,
Bank of America, N.A., as administrative agent, and the lenders party thereto (incorporated by reference to
Exhibit 10.1 to the Company’s Current Report on Form 8-K filed on June 3, 2019).
Amendment No. 1, dated as of May 7, 2020, to the Term Loan Credit Agreement, dated June 3, 2019, among the
Company, Bank of America, N.A. as administrative agent, and the lenders party thereto. (incorporated herein by
reference to Exhibit 10.1 to the Company’s Quarterly Report on Form 10-Q filed on May 8, 2020).
Executive Employment Agreement, dated June 4, 2019, by and between Laboratory Corporation of America
Holdings and Adam H. Schechter (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on
Form 8-K filed on June 5, 2019).
Amended and Restated Master Senior Executive Severance Plan.
Letter of PricewaterhouseCoopers LLP, dated November 5, 2020 (incorporated by reference to Exhibit 16.1 to
the Company’s Current Report on Form 8-K filed on November 5, 2020).
List of Subsidiaries of the Company
Consent of PricewaterhouseCoopers LLP, an independent registered public accounting firm
Power of Attorney of Kerrii B. Anderson
Power of Attorney of Jean-Luc Bélingard
Power of Attorney of Jeffrey A. Davis
Power of Attorney of D. Gary Gilliland, M.D., Ph.D.
Power of Attorney of Garheng Kong, M.D., Ph.D.
Power of Attorney of Peter M. Neupert
Power of Attorney of Richelle P. Parham
Power of Attorney of R. Sanders Williams, M.D.
Certification by the Chief Executive Officer pursuant to Rule 13a-14(a) or Rule 15d-14(a)
Certification by the Chief Financial Officer pursuant to Rule 13a-14(a) or Rule 15d-14(a)
Written Statement of Chief Executive Officer and Chief Financial Officer pursuant to Section 906 of the
Sarbanes-Oxley Act of 2002 (18 U.S.C. Section 1350)
101.INS*
101.SCH*
101.CAL*
101.DEF*
101.LAB*
101.PRE*
104*
Inline XBRL Instance Document - The instance document does not appear in the Interactive Data File because
its XBRL tags are embedded within the Inline XBRL document.
Inline XBRL Taxonomy Extension Schema
Inline XBRL Taxonomy Extension Calculation Linkbase
Inline XBRL Taxonomy Extension Definition Linkbase
Inline XBRL Taxonomy Extension Label Linkbase
Inline XBRL Taxonomy Extension Presentation Linkbase
Cover Page Interactive Data File (embedded within the Inline XBRL document)
*
+
Filed or furnished herewith, as required
Management contracts or compensatory plans or arrangements
67
Index
Item 16.
FORM 10-K SUMMARY
None.
68
Index
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this
Annual Report to be signed on its behalf by the undersigned, thereunto duly authorized.
SIGNATURES
LABORATORY CORPORATION OF AMERICA HOLDINGS
Registrant
By:
/s/ ADAM H. SCHECHTER
Adam H. Schechter
President and Chief Executive Officer
Dated: February 25, 2021
69
Index
Pursuant to the requirements of the Securities Exchange Act of 1934, this Annual Report has been signed below by the
following persons on behalf of the registrant on February 25, 2021 in the capacities indicated.
Signature
Title
/s/ ADAM H. SCHECHTER
Adam H. Schechter
/s/ GLENN A. EISENBERG
Glenn A. Eisenberg
/s/ PETER J. WILKINSON
Peter J. Wilkinson
*
Kerrii B. Anderson
*
Jean-Luc Bélingard
*
Jeffrey A. Davis
*
D. Gary Gilliland, M.D., Ph.D.
*
Garheng Kong, M.D., Ph.D.
*
Peter M. Neupert
*
Richelle Parham
*
R. Sanders Williams, M.D.
President and Chief Executive Officer
(Principal Executive Officer)
Executive Vice President, Chief Financial Officer
(Principal Financial Officer)
Senior Vice President and Chief Accounting Officer
(Principal Accounting Officer)
Director
Director
Director
Director
Director
Director
Director
Director
* Sandra van der Vaart, by her signing her name hereto, does hereby sign this Annual Report on behalf of the directors of the
Registrant after whose typed names asterisks appear, pursuant to powers of attorney duly executed by such directors and filed
with the Securities and Exchange Commission.
By:
/s/ Sandra van der Vaart
Sandra van der Vaart
Attorney-in-fact
70
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
INDEX TO CONSOLIDATED FINANCIAL STATEMENTS
Report of Independent Registered Public Accounting Firm
Consolidated Financial Statements:
Consolidated Balance Sheets
Consolidated Statements of Operations
Consolidated Statements of Comprehensive Earnings
Consolidated Statements of Changes in Shareholders' Equity
Consolidated Statements of Cash Flows
Notes to Consolidated Financial Statements
Page
F-2
F-5
F-6
F-7
F-8
F-9
F-10
F-1
Index
Report of Independent Registered Public Accounting Firm
To the Board of Directors and Shareholders of Laboratory Corporation of America Holdings
Opinions on the Financial Statements and Internal Control over Financial Reporting
We have audited the accompanying consolidated balance sheets of Laboratory Corporation of America Holdings and its
subsidiaries (the “Company”) as of December 31, 2020 and 2019, and the related consolidated statements of operations,
comprehensive earnings, changes in shareholders' equity and cash flows for each of the three years in the period ended
December 31, 2020, including the related notes (collectively referred to as the “consolidated financial statements”). We also
have audited the Company's internal control over financial reporting as of December 31, 2020, based on criteria established in
Internal Control - Integrated Framework (2013) issued by the Committee of Sponsoring Organizations of the Treadway
Commission (COSO).
In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial
position of the Company as of December 31, 2020 and 2019, and the results of its operations and its cash flows for each of the
three years in the period ended December 31, 2020 in conformity with accounting principles generally accepted in the United
States of America. Also in our opinion, the Company maintained, in all material respects, effective internal control over
financial reporting as of December 31, 2020, based on criteria established in Internal Control - Integrated Framework (2013)
issued by the COSO.
Change in Accounting Principle
As discussed in Note 1 to the consolidated financial statements, the Company changed the manner in which it accounts for
leases in 2019.
Basis for Opinions
The Company's management is responsible for these consolidated financial statements, for maintaining effective internal
control over financial reporting, and for its assessment of the effectiveness of internal control over financial reporting, included
in the Report of Management on Internal Control over Financial Reporting appearing under Item 9A. Our responsibility is to
express opinions on the Company’s consolidated financial statements and on the Company's internal control over financial
reporting based on our audits. We are a public accounting firm registered with the Public Company Accounting Oversight
Board (United States) (PCAOB) and are required to be independent with respect to the Company in accordance with the U.S.
federal securities laws and the applicable rules and regulations of the Securities and Exchange Commission and the PCAOB.
We conducted our audits in accordance with the standards of the PCAOB. Those standards require that we plan and perform the
audits to obtain reasonable assurance about whether the consolidated financial statements are free of material misstatement,
whether due to error or fraud, and whether effective internal control over financial reporting was maintained in all material
respects.
Our audits of the consolidated financial statements included performing procedures to assess the risks of material misstatement
of the consolidated financial statements, whether due to error or fraud, and performing procedures that respond to those risks.
Such procedures included examining, on a test basis, evidence regarding the amounts and disclosures in the consolidated
financial statements. Our audits also included evaluating the accounting principles used and significant estimates made by
management, as well as evaluating the overall presentation of the consolidated financial statements. Our audit of internal
control over financial reporting included obtaining an understanding of internal control over financial reporting, assessing the
risk that a material weakness exists, and testing and evaluating the design and operating effectiveness of internal control based
on the assessed risk. Our audits also included performing such other procedures as we considered necessary in the
circumstances. We believe that our audits provide a reasonable basis for our opinions.
Definition and Limitations of Internal Control over Financial Reporting
A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the
reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally
accepted accounting principles. A company’s internal control over financial reporting includes those policies and procedures
that (i) pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and
dispositions of the assets of the company; (ii) provide reasonable assurance that transactions are recorded as necessary to permit
preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and
F-2
Index
expenditures of the company are being made only in accordance with authorizations of management and directors of the
company; and (iii) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or
disposition of the company’s assets that could have a material effect on the financial statements.
Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also,
projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate
because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.
Critical Audit Matters
The critical audit matters communicated below are matters arising from the current period audit of the consolidated financial
statements that were communicated or required to be communicated to the audit committee and that (i) relate to accounts or
disclosures that are material to the consolidated financial statements and (ii) involved our especially challenging, subjective, or
complex judgments. The communication of critical audit matters does not alter in any way our opinion on the consolidated
financial statements, taken as a whole, and we are not, by communicating the critical audit matters below, providing separate
opinions on the critical audit matters or on the accounts or disclosures to which they relate.
Valuation of Labcorp Diagnostics Segment (Dx) Net Accounts Receivable
As described in Notes 2 and 7 to the consolidated financial statements, the Dx business’s revenues are distributed among four
payer portfolios - clients, patients, Medicare and Medicaid, and third-party. Dx accounts receivable due from these payer
portfolios was $1,515.5 million as of December 31, 2020. Management has a formal process to estimate implicit price
concessions for uncollectable accounts. Management considers negotiated discounts and anticipated adjustments, including
historical collection experience for each of the payer portfolios, when revenues and accounts receivable are recorded.
Anticipated write-offs are recorded as an adjustment to revenue and at an amount considered necessary to record the revenue at
its net realizable value. In addition to contractual discounts, other adjustments including anticipated payer denials and other
external factors that could affect the collectibility of its receivables are considered when determining revenue and the net
receivable amount.
The principal considerations for our determination that performing procedures relating to the valuation of Dx net accounts
receivable is a critical audit matter are the significant judgment and estimation by management to determine net accounts
receivable related to the Dx segment, which led to a high degree of auditor judgment, subjectivity and effort in performing
procedures and in evaluating the audit evidence related to the valuation of net Dx accounts receivable.
Addressing the matter involved performing procedures and evaluating audit evidence in connection with forming our overall
opinion on the consolidated financial statements. These procedures included testing the effectiveness of controls relating to the
valuation of Dx net accounts receivable. These procedures also included, among others, testing management's process for
developing the estimate of net accounts receivable, and the relevance of historical billing and collection data as an input to the
analysis; testing the accuracy of a sample of revenue transactions and a sample of cash collections from the historical billing
and collection data which is used in management’s analysis; and performing a retrospective comparison of actual cash
collected to the prior year estimate of net accounts receivable.
Revenue Recognition - Estimating Costs to Complete for Clinical Research Services
As described in Note 21 to the consolidated financial statements, Labcorp Drug Development (DD) revenue was $4,877.7
million for the year ended December 31, 2020. Clinical services utilizing the input-based measure of progress account for 50%
of DD revenue. The majority of clinical development and commercialization service long-term contracts within the DD
segment are service contracts for clinical research that represent a single performance obligation (e.g., management of a clinical
study). Revenue for these service contracts is recognized over time based on the progress of the performance obligation which
was measured by the proportion of the actual costs incurred to the total costs expected to complete the contract (including labor
and pass-through costs such as investigator grants and reimbursable out-of-pocket expenses). This cost-based method of
revenue recognition required management to estimate the costs to complete these service contracts on an ongoing basis.
The principal considerations for our determination that performing procedures relating to estimating costs to complete for
clinical research services is a critical audit matter are the significant judgment and estimation by management when developing
the costs to complete, including the labor and third party costs to complete the service contracts, which led to a high degree of
auditor judgment, subjectivity and effort in performing procedures and in evaluating evidence related to the cost estimates made
by management.
F-3
Index
Addressing the matter involved performing procedures and evaluating audit evidence in connection with forming our overall
opinion on the consolidated financial statements. These procedures included testing the effectiveness of controls relating to the
revenue recognition process, including controls over the estimated costs to complete. These procedures also included, among
others, testing management's process for estimating cost to complete the service contracts, testing, for certain contracts, actual
costs incurred and evaluating the reasonableness of management’s estimation of costs to complete projects, including labor and
third party costs to complete service contracts; and evaluating whether the assumptions used were reasonable by performing a
retrospective comparison of current year project costs to historical cost estimates made by management.
Goodwill Impairment Assessment - Two Reporting Units within the DD Segment
As described in Notes 1 and 9 to the consolidated financial statements, the Company’s consolidated goodwill balance was
$7,751.5 million as of December 31, 2020, and the goodwill associated with the Company’s DD segment was $3,951.3 million.
For the year ended December 31, 2020, the Company recorded goodwill impairment of $418.7 million for one of its reporting
units within the DD segment. Management assesses goodwill for impairment at least annually or whenever events or changes in
circumstances indicate that the carrying amount of such assets may not be recoverable. The Company recognizes an impairment
charge for the amount by which the reporting unit's carrying amount exceeds its fair value. Fair value of a reporting unit is
estimated using both income-based and market-based valuation methods. Management’s impairment analysis for certain
reporting units utilized significant judgments and assumptions related to the market comparable method analysis, such as
selected market multiples, and related to cash flow projections, such as revenue and terminal growth rates, projected operating
margin, and the discount rate.
The principal considerations for our determination that performing procedures relating to the goodwill impairment assessment
of the two reporting units within the DD segment is a critical audit matter are the significant judgment by management when
developing the fair value estimate of the reporting units, which led to a high degree of auditor judgment, subjectivity, and audit
effort in performing procedures to evaluate management’s market comparable method analysis and cash flow projections,
including significant assumptions for the selected market multiples, revenue and terminal growth rates, projected operating
margin, and the discount rate. Also, the audit effort involved the use of professionals with specialized skill and knowledge to
assist in performing these procedures and evaluating the audit evidence obtained from these procedures.
Addressing the matter involved performing procedures and evaluating audit evidence in connection with forming our overall
opinion on the consolidated financial statements. These procedures included testing the effectiveness of controls relating to
management’s goodwill impairment assessment, including controls over the significant assumptions used in the valuation of the
reporting units. These procedures also included, among others, testing management's process for estimating the fair value of the
reporting units which involved evaluating the appropriateness of the valuation methods and the reasonableness of significant
assumptions used in the market comparable method analysis and cash flow projections, including the selected market multiples,
revenue and terminal growth rates, projected operating margin, and the discount rate. Evaluating the reasonableness of the
revenue and terminal growth rates and projected operating margin involved considering the past performance of the reporting
unit and considering whether these assumptions were consistent with evidence obtained in other areas of the audit.
Professionals with specialized skill and knowledge were used to assist in the evaluation of the appropriateness of the
Company’s valuation methods and the reasonableness of (i) the terminal growth rates impacting the reporting units' future cash
flows, (ii) the selected market multiple applied to the reporting units' financial information and (iii) the discount rate.
/s/ PricewaterhouseCoopers LLP
Raleigh, North Carolina
February 25, 2021
We have served as the Company’s auditor since 1997.
F-4
Index
PART I – FINANCIAL INFORMATION
Item 1. Financial Information
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
(In Millions)
December 31,
2020
December 31,
2019
$
1,320.8 $
337.5
2,479.8
536.8
423.2
364.8
5,125.4
2,729.6
7,751.5
3,961.1
73.5
20.6
410.0
20,071.7 $
638.9 $
1,357.7
506.5
192.0
6.7
376.7
3,078.5
5,419.0
677.6
84.4
905.4
526.4
10,691.3
1,543.9
481.4
244.7
373.7
2,981.2
2,636.6
7,865.0
4,034.5
84.9
8.8
435.4
18,046.4
632.3
942.4
451.0
206.5
8.4
415.2
2,655.8
5,789.8
596.6
91.1
942.8
383.2
10,459.3
20.7
20.1
9.0
110.3
9,402.3
(161.9)
9,359.7
20,071.7 $
9.0
26.8
7,903.6
(372.4)
7,567.0
18,046.4
$
$
$
ASSETS
Current assets:
Cash and cash equivalents
Accounts receivable, net of allowance for doubtful accounts of $22.1 and $19.0 as of
December 31, 2020 and 2019, respectively
Unbilled services
Supplies inventory
Prepaid expenses and other
Total current assets
Property, plant and equipment, net
Goodwill, net
Intangible assets, net
Joint venture partnerships and equity method investments
Deferred income taxes
Other assets, net
Total assets
LIABILITIES AND SHAREHOLDERS’ EQUITY
Current liabilities:
Accounts payable
Accrued expenses and other
Unearned revenue
Short-term operating lease liabilities
Short-term finance lease liabilities
Short-term borrowings and current portion of long-term debt
Total current liabilities
Long-term debt, less current portion
Operating lease liabilities
Financing lease liabilities
Deferred income taxes and other tax liabilities
Other liabilities
Total liabilities
Commitments and contingent liabilities
Noncontrolling interest
Shareholders’ equity
Common stock, 97.5 and 97.2 shares outstanding at December 31, 2020 and 2019,
respectively
Additional paid-in capital
Retained earnings
Accumulated other comprehensive loss
Total shareholders’ equity
Total liabilities and shareholders’ equity
The accompanying notes are an integral part of these consolidated financial statements.
F-5
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF OPERATIONS
(In Millions, Except Per Share Data)
Revenues
Cost of revenues
Gross profit
Selling, general and administrative expenses
Amortization of intangibles and other assets
Goodwill and other asset impairments
Restructuring and other charges
Operating income
Other income (expense):
Interest expense
Equity method income, net
Investment income
Other, net
Earnings before income taxes
Provision for income taxes
Net earnings
Less: Net earnings attributable to the noncontrolling interest
Net earnings attributable to Laboratory Corporation of America Holdings
Basic earnings per common share
Diluted earnings per common share
2018
2020
Years Ended December 31,
2019
$ 13,978.5 $ 11,554.8 $ 11,333.4
8,157.0
3,176.4
1,570.9
231.7
—
48.1
1,325.7
9,025.7
4,952.8
1,729.3
275.4
462.1
40.6
2,445.4
8,302.3
3,252.5
1,624.5
243.2
—
54.6
1,330.2
(207.4)
2.9
10.3
(32.1)
2,219.1
662.1
1,557.0
(240.7)
9.8
8.8
(3.2)
1,104.9
280.0
824.9
(0.9)
1,556.1 $
(1.1)
823.8 $
(244.2)
11.6
7.5
167.7
1,268.3
384.4
883.9
(0.2)
883.7
15.99 $
15.88 $
8.42 $
8.35 $
8.71
8.61
$
$
$
The accompanying notes are an integral part of these consolidated financial statements.
F-6
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF COMPREHENSIVE EARNINGS
(In Millions, Except Per Share Data)
Net earnings
Foreign currency translation adjustments
Net benefit plan adjustments
Other comprehensive earnings (loss) before tax
Provision for income tax related to items of comprehensive earnings
Other comprehensive earnings (loss), net of tax
Comprehensive earnings
Less: Net earnings attributable to the noncontrolling interest
Years Ended December 31,
2020
2019
2018
$ 1,557.0 $
264.1
(65.7)
198.4
12.1
210.5
1,767.5
(0.9)
824.9 $
104.4
(17.4)
87.0
3.7
90.7
915.6
(1.1)
883.9
(176.6)
29.3
(147.3)
17.9
(129.4)
754.5
(0.2)
Comprehensive earnings attributable to Laboratory Corporation of America Holdings
$ 1,766.6 $
914.5 $
754.3
The accompanying notes are an integral part of these consolidated financial statements.
F-7
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS’ EQUITY
(In Millions)
Common
Stock
Additional
Paid-in
Capital
Retained
Earnings
Treasury
Stock
Accumulated
Other
Comprehensive
Earnings (Loss)
Total
Shareholders’
Equity
BALANCE AT DECEMBER 31, 2017
$
12.0 $ 1,989.8 $ 6,196.1 $ (1,060.1) $
(333.7) $
6,804.1
Net earnings attributable to Laboratory Corporation of America
Holdings
Other comprehensive loss, net of tax
Issuance of common stock under employee stock plans
Net share settlement tax payments from issuance of stock to employees
Conversion of zero-coupon convertible debt
Stock compensation
Purchase of common stock
BALANCE AT DECEMBER 31, 2018
Net earnings attributable to Laboratory Corporation of America
Holdings
Other comprehensive earnings, net of tax
Issuance of common stock under employee stock plans
Net share settlement tax payments from issuance of stock to employees
Stock compensation
Retirement of treasury stock
Purchase of common stock
BALANCE AT DECEMBER 31, 2019
Adoption of credit loss accounting standard
Net earnings attributable to Laboratory Corporation of America
Holdings
Other comprehensive earnings, net of tax
Issuance of common stock under employee stock plans
Net share settlement tax payments from issuance of stock to employees
Stock compensation
Purchase of common stock
—
—
—
—
—
—
(0.3)
11.7
—
—
—
—
—
(2.4)
(0.3)
9.0
—
—
—
—
—
—
—
—
69.1
—
0.3
91.6
(699.7)
883.7
—
—
—
—
—
—
—
—
—
(48.0)
—
—
—
—
(129.4)
—
—
—
—
—
1,451.1
7,079.8
(1,108.1)
(463.1)
—
—
64.7
(0.5)
107.0
(1,145.8)
(449.7)
823.8
—
—
—
—
—
26.8
—
7,903.6
(7.0)
—
—
55.9
(34.5)
111.7
(49.6)
1,556.1
—
—
—
—
(50.4)
—
—
—
(40.1)
—
1,148.2
—
—
—
—
—
—
—
—
—
—
90.7
—
—
—
—
—
(372.4)
—
—
210.5
—
—
—
—
883.7
(129.4)
69.1
(48.0)
0.3
91.6
(700.0)
6,971.4
823.8
90.7
64.7
(40.6)
107.0
—
(450.0)
7,567.0
(7.0)
1,556.1
210.5
55.9
(34.5)
111.7
(100.0)
BALANCE AT DECEMBER 31, 2020
$
9.0 $
110.3 $ 9,402.3 $
— $
(161.9) $
9,359.7
The accompanying notes are an integral part of these consolidated financial statements.
F-8
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CASH FLOWS
(In Millions)
Years Ended December 31,
2018
2019
2020
$ 1,557.0 $ 824.9 $ 883.9
624.7
111.7
—
200.3
462.1
(47.0)
83.4
577.2
107.0
13.2
194.1
—
29.2
(6.5)
552.1
91.6
(184.9)
—
—
22.2
10.8
(913.4)
(42.5)
(196.6)
(5.4)
(5.3)
48.4
257.9
2,135.3
(64.1)
(59.0)
(21.9)
(42.6)
(12.8)
38.1
(132.1)
50.2
(81.0)
(18.9)
(57.9)
43.3
(33.8)
27.8
1,305.4
1,444.7
(381.7)
(400.2)
(40.1)
(27.5)
42.1
7.7
1.0
11.2
—
—
3.1
1.7
(876.0)
(267.6)
(643.2) (1,283.1)
(379.8)
(22.3)
50.1
—
658.2
18.3
(117.8)
206.7
—
—
—
151.7
(151.7)
(412.2)
—
(34.5)
55.9
(100.0)
(26.6)
(517.4)
8.6
983.3
337.5
—
1,050.0
—
850.0
(295.0)
(1,002.0)
467.2
495.0
(467.2)
(495.0)
(400.0)
(687.9)
—
(11.6)
(48.0)
(40.6)
69.1
64.7
(700.0)
(450.0)
(25.3)
(16.0)
(252.7) (1,389.9)
(12.0)
110.2
316.6
$ 1,320.8 $ 337.5 $ 426.8
1.8
(89.3)
426.8
CASH FLOWS FROM OPERATING ACTIVITIES:
Net earnings
Adjustments to reconcile net earnings to net cash provided by operating activities:
Depreciation and amortization
Stock compensation
Loss (gain) on sale of business
Operating lease right-of-use asset expense
Goodwill and other asset impairments
Deferred income taxes
Other, net
Change in assets and liabilities (net of effects of acquisitions and divestitures):
(Increase) decrease in accounts receivable
Increase in unbilled services
Increase in inventory
Increase in prepaid expenses and other
Increase (decrease) in accounts payable
Increase (decrease) in deferred revenue
Increase (decrease) in accrued expenses and other
Net cash provided by operating activities
CASH FLOWS FROM INVESTING ACTIVITIES:
Capital expenditures
Purchases of investments
Proceeds from sale of assets
Proceeds from sale or distributions of investments
Proceeds from sale of business
Proceeds from exit of swaps
Acquisition of businesses, net of cash acquired
Net cash (used for) provided by investing activities
CASH FLOWS FROM FINANCING ACTIVITIES:
Proceeds from Senior Notes offerings
Proceeds from term loan
Payments on term loan
Proceeds from revolving credit facilities
Payments on revolving credit facilities
Payments on Senior Notes
Payment of debt issuance costs
Net share settlement tax payments from issuance of stock to employees
Net proceeds from issuance of stock to employees
Purchase of common stock
Other
Net cash used for financing activities
Effect of exchange rate changes on cash and cash equivalents
Net increase (decrease) in cash and cash equivalents
Cash and cash equivalents at beginning of period
Cash and cash equivalents at end of period
The accompanying notes are an integral part of these consolidated financial statements.
F-9
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
1. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Basis of Financial Statement Presentation
Laboratory Corporation of America® Holdings (Labcorp® or the Company) is a leading global life sciences company that
provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and
confident decisions. By leveraging its strong diagnostics and drug development capabilities, the Company provides insights and
accelerates innovations to improve health and improve lives. With over 72,400 employees, the Company serves clients in more
than 100 countries.
The Company reports its business in two segments, Labcorp Diagnostics (Dx) and Labcorp Drug Development (DD). As
part of the Company's rebranding initiative announced in December 2020, the Company changed the names of its segments,
which were previously referred to as LabCorp Diagnostics and Covance Drug Development. For further financial information
about these segments, including information for each of the last three fiscal years regarding revenue, operating income, and
other important information, see Note 21 Business Segment Information to the Consolidated Financial Statements. In 2020, Dx
and DD contributed 65% and 35%, respectively, of revenues to the Company, and in 2019 contributed 60% and 40%,
respectively.
The consolidated financial statements include the accounts of the Company and its majority-owned subsidiaries for which it
exercises control. Long-term investments in affiliated companies in which the Company exercises significant influence, but
which it does not control, are accounted for using the equity method. Investments in which the Company does not exercise
significant influence (generally, when the Company has an investment of less than 20% and no representation on the investee's
board of directors) are accounted for at fair value or at cost minus impairment adjusted for observable price changes in orderly
transactions for an identical or similar investment of the same issuer for those investments that do not have readily determinable
fair values. All significant inter-company transactions and accounts have been eliminated. The Company does not have any
variable interest entities or special purpose entities whose financial results are not included in the consolidated financial
statements.
The financial statements of the Company's operating foreign subsidiaries are measured using the local currency as the
functional currency. Assets and liabilities are translated at exchange rates as of the balance sheet date. Revenues and expenses
are translated at average monthly exchange rates prevailing during the year. Resulting translation adjustments are included in
“Accumulated other comprehensive income.”
Recently Adopted Guidance
In June 2016, the FASB issued a new accounting standard intended to provide financial statement users with more decision-
useful information about expected credit losses and other commitments to extend credit held by the reporting entity. The
standard replaces the incurred loss impairment methodology in current generally accepted accounting principles (GAAP) with
one that reflects expected credit losses and requires consideration of a broader range of reasonable and supportable information
to inform credit loss estimates. The Company recorded an opening retained earnings adjustment of $7.0 with the adoption of
this standard on January 1, 2020.
In August 2018, the FASB issued a new accounting standard to reduce, modify, and add to the disclosure requirements on
fair value measurements. The Company adopted this standard effective January 1, 2020. The adoption of this standard did not
have a material impact on the consolidated financial statements.
In August 2018, the FASB issued a new accounting standard to align the requirements for capitalizing implementation costs
incurred in a hosting arrangement that is a service contract with the requirements for capitalizing implementation costs incurred
to develop or obtain internal-use software. The Company adopted this standard effective January 1, 2020. The adoption of this
standard did not have a material impact on the consolidated financial statements.
In August 2018, the FASB issued a new accounting standard to modify the disclosure requirements for employers that
sponsor defined benefit pension or other postretirement plans. The Company adopted this standard effective January 1, 2020.
The adoption of this standard did not have a material impact on the consolidated financial statements.
Novel Coronavirus (COVID-19) Financial Statement Impact
In March 2020, COVID-19 was declared a pandemic. COVID-19 has had and continues to have an extensive impact on the
global health and economic environments. During 2020, the Company recorded goodwill and other asset impairment charges of
$462.1, $450.5 within DD and $11.6 within Dx, as a result of the COVID-19 pandemic. The Company concluded that the fair
F-10
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
value was less than carrying value for two of its reporting units and recorded goodwill impairment of $418.7 and $3.7 for DD
and Dx, respectively. Additional impairment of identifiable intangible and tangible assets of $31.8 and $7.9 was recorded for
DD and Dx, respectively, for impairment of a tradename, software, customer relationships, technology assets and a note
receivable. The Company also impaired certain of the Company's investments by a total of $25.4 during 2020 due to the impact
of COVID-19; $7.1 was included in Equity method earnings (loss), net and $18.3 was included in Other, net.
In April 2020, the Company received cash payments of approximately $55.9 from the Public Health and Social Services
Emergency Fund for provider relief that was appropriated by Congress to the U.S. Department of Health and Human Services
(HHS) in the Coronavirus Aid, Relief, and Economic Security Act (CARES Act Provider Relief Funds). In August 2020, the
Company received an additional $76.2 in CARES Act Provider Relief Funds. As the Company's Diagnostic business
demonstrated recovery and demand for COVID-19 testing increased, the Company determined that the negative financial
impact of COVID-19 which the CARES Act Provider Relief Funds were designed to address no longer applied to the
Company. As a result, the Company returned the CARES Act Provider Relief Funds, to the government in the fourth quarter of
2020. There was no impact to the Company's consolidated financial statements as of December 31, 2020 and for the year then
ended.
Reimbursable Out-of-Pocket Expenses
DD pays on behalf of its customers certain out-of-pocket costs for which the Company is reimbursed at cost, without mark-
up or profit. Out-of-pocket costs paid by DD are reflected in operating expenses, while the reimbursements received are
reflected in revenues in the consolidated statements of operations.
Cost of Revenues
Cost of revenue includes direct labor and related benefit charges, other direct costs, shipping and handling fees, and an
allocation of facility charges and information technology costs. Selling, general and administrative expenses consist primarily
of administrative payroll and related benefit charges, advertising and promotional expenses, administrative travel and an
allocation of facility charges and information technology costs. Cost of advertising is expensed as incurred.
Use of Estimates
The preparation of financial statements in conformity with generally accepted accounting principles requires the Company
to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets
and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reported
periods. Significant estimates include implicit price concessions, revenue estimates, the allowances for doubtful accounts,
deferred tax assets, fair values of acquired assets and assumed liabilities in business combinations, fair value of goodwill and
indefinite-lived intangible assets, amortization lives for acquired intangible assets, and accruals for self-insurance reserves,
litigation reserves and pensions. The allowance for doubtful accounts is determined based on historical collections trends, the
aging of accounts, current economic conditions and regulatory changes. Actual results could differ from those estimates.
The extent to which the COVID-19 pandemic has and will continue to impact the Company’s business and financial results
depend on numerous evolving factors including, but not limited to: the magnitude and duration of the COVID-19 pandemic, the
impact to worldwide macroeconomic conditions including interest rates, employment rates and health insurance coverage, the
speed of the anticipated recovery, and governmental and business reactions to the pandemic. The Company assessed certain
accounting matters that generally require consideration of forecasted financial information in context with the information
reasonably available to the Company and the unknown future impacts of COVID-19 as of December 31, 2020, and through the
date of this Annual Report. The accounting matters assessed included, but were not limited to, the Company’s implicit price
concessions and credit losses, equity investments, notes receivable and the carrying value of goodwill and other long-lived
assets. The Company’s future assessment of the magnitude and duration of COVID-19, as well as other factors, could result in
additional material impacts to the Company’s consolidated financial statements in future reporting periods
Concentration of Credit Risk
Financial instruments that potentially subject the Company to concentrations of credit risk consist primarily of cash and
cash equivalents and accounts receivable.
The Company maintains cash and cash equivalents with various major financial institutions. The total cash and cash
equivalent balances that exceeded the balances insured by the Federal Deposit Insurance Commission, were approximately
$1,319.4 and $335.0 at December 31, 2020, and 2019, respectively.
Substantially all of the Company’s accounts receivable are with companies in the healthcare or biopharmaceutical industry
and individuals. However, concentrations of credit risk are mitigated due to the number of the Company’s customers as well as
their dispersion across many different geographic regions.
F-11
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Although Dx has receivables due from U.S. and state governmental agencies, the Company does not believe that such
receivables represent a credit risk since the related healthcare programs are funded by U.S. and state governments, and payment
is primarily dependent upon submitting appropriate documentation. Accounts receivable balances (gross) from Medicare and
Medicaid were $109.8 and $81.4 at December 31, 2020, and 2019, respectively.
For the Company's operations in Ontario, Canada, the Ontario Ministry of Health and Long-Term Care (Ministry)
determines who can establish a licensed community medical laboratory and caps the amount that each of these licensed
laboratories can bill the government sponsored healthcare plan. The Ontario government-sponsored healthcare plan covers the
cost of commercial laboratory testing performed by the licensed laboratories. The provincial government discounts the annual
testing volumes based on certain utilization discounts and establishes an annual maximum it will pay for all community
laboratory tests. The agreed-upon reimbursement rates are subject to Ministry review at the end of year and can be adjusted (at
the government's discretion) based upon the actual volume and mix of test work performed by the licensed healthcare providers
in the province during the year. The capitated accounts receivable balances from the Ontario government sponsored healthcare
plan were CAD 0.6 and CAD 3.2 at December 31, 2020, and 2019, respectively.
The portion of the Company's accounts receivable due from patients comprises the largest portion of credit risk. At
December 31, 2020, and 2019, receivables due from patients represented approximately 13.9% and 21.1% of the Company's
consolidated gross accounts receivable, respectively. The Company applies assumptions and judgments including historical
collection experience and reasonable and supportable forecasts for assessing collectability and determining allowances for
doubtful accounts for accounts receivable from patients.
Earnings per Share
Basic earnings per share is computed by dividing net earnings attributable to Laboratory Corporation of America Holdings
by the weighted average number of common shares outstanding. Diluted earnings per share is computed by dividing net
earnings including the impact of dilutive adjustments by the weighted average number of common shares outstanding plus
potentially dilutive shares, as if they had been issued at the earlier of the date of issuance or the beginning of the period
presented. Potentially dilutive common shares result primarily from the Company’s outstanding stock options, restricted stock
awards, performance share awards, and shares issuable upon conversion of zero-coupon subordinated notes.
The following represents a reconciliation of basic earnings per share to diluted earnings per share:
Basic earnings per share
Stock options and stock awards
Effect of convertible debt, net of tax
Diluted earnings per share
Income
$ 1,556.1
—
—
$ 1,556.1
2020
2019
Per
Share
Amount
Shares
Income
97.3 $ 15.99 $ 823.8
—
0.7
—
—
98.0 $ 15.88 $ 823.8
Per
Share
Amount
Shares
Income
97.9 $ 8.42 $ 883.7
—
0.7
—
—
98.6 $ 8.35 $ 883.7
2018
Per
Share
Shares
Amount
101.4 $ 8.71
1.2
—
102.6 $ 8.61
The following table summarizes the potential common shares not included in the computation of diluted earnings per share
because their impact would have been antidilutive:
Stock options
Stock Compensation Plans
Years Ended December 31,
2019
0.2
2018
0.1
2020
0.2
The Company measures stock compensation cost for all equity awards at fair value on the date of grant and recognizes
compensation expense over the service period for awards expected to vest. The fair value of restricted stock units is determined
based on the number of shares granted and the quoted price of the Company’s common stock on the grant date. The grant date
fair value of performance awards is based on a Monte Carlo simulated fair value for the relative (as compared to the peer
companies) total shareholder return component of the performance awards. Such value is recognized as an expense over the
service period, net of estimated forfeitures and the Company's determination of whether it is probable that the performance
targets will be achieved. At the end of each reporting period, the Company reassesses the probability of achieving performance
targets. The estimation of equity awards that will ultimately vest requires judgment and the Company considers many factors
when estimating expected forfeitures, including types of awards, employee class, and historical experience. Forfeitures are
recognized as a reduction of compensation expense in earnings in the period in which they occur.
F-12
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
See Note 15 Stock Compensation Plans for assumptions used in calculating compensation expense for the Company’s stock
compensation plans.
Cash Equivalents
Cash and cash equivalents consist of highly liquid instruments, such as commercial paper, time deposits, and other money
market instruments, substantially all of which have maturities when purchased of three months or less.
Supplies Inventory
Inventories, consisting primarily of purchased laboratory and customer supplies and finished goods, are stated at the lower
of cost (first-in, first-out) or net realizable value. Supplies accounted for $403.6 and $228.3 and finished goods accounted for
$19.6 and $16.4 of total inventory at December 31, 2020, and 2019, respectively. The Company's inventory reserve balance was
$20.2 and $0.0, as of December 31, 2020 and 2019, respectively. Once recorded, the reserves are considered permanent
adjustments to the carrying value of inventory.
Property, Plant and Equipment
Property, plant and equipment are recorded at cost. Depreciation and amortization expense is computed on all classes of
assets based on their estimated useful lives, as indicated below, using the straight-line method.
Buildings and building improvements
Machinery and equipment
Furniture and fixtures
Software
Years
10 - 40
3 - 10
5 - 10
3 - 10
Leasehold improvements are amortized over the shorter of their estimated useful lives or the term of the related leases.
Expenditures for repairs and maintenance are charged to operations as incurred. Retirements, sales and other disposals of assets
are recorded by removing the cost and accumulated depreciation from the related accounts with any resulting gain or loss
reflected in the consolidated statements of operations.
Capitalized Software Costs
The Company capitalizes purchased software that is ready for service and capitalizes software development costs incurred
on significant projects starting from the time that the preliminary project stage is completed and the Company commits to
funding a project until the project is substantially complete and the software is ready for its intended use. Capitalized costs
include direct material and service costs and payroll and payroll-related costs. Research and development (R&D) costs and
other computer software maintenance costs related to software development are expensed as incurred. Capitalized software
costs are amortized using the straight-line method over the estimated useful life of the underlying system ranging from three to
ten years, generally five years. Amortization begins once the underlying system is substantially complete and ready for its
intended use.
Long-Lived Assets
The Company assesses goodwill and indefinite-lived intangibles for impairment at least annually or whenever events or
changes in circumstances indicate that the carrying amount of such assets may not be recoverable. The Company recognizes an
impairment charge for the amount by which the reporting unit's carrying amount exceeds its fair value.
Based upon the revised forecasted revenues and operating income following the declaration of the COVID-19 global
pandemic, management concluded there was a triggering event and updated its annual 2019 goodwill impairment testing as of
March 31, 2020, for certain of its DD reporting units and Dx reporting units. Based on the quantitative impairment assessment
performed in the same manner as our annual quantitative assessment, the Company concluded that the fair value was less than
carrying value for two of its reporting unit and recorded a goodwill impairment of $418.7 for DD and $3.7 for Dx.
Management performed its annual goodwill and intangible asset impairment testing as of the beginning of the fourth quarter
of 2020. The Company elected to perform the qualitative assessment for goodwill and intangible assets for the domestic Dx
reporting units and certain DD reporting units, a quantitative assessment for two of the DD reporting units and a quantitative
assessment for the Canadian reporting unit and its indefinite-lived assets consisting of acquired Canadian licenses.
In the qualitative assessment, the Company considered relevant events and circumstances for each reporting unit, including
(i) current year results, (ii) financial performance versus management’s annual and five-year strategic plans, (iii) changes in the
reporting unit carrying value since prior year, (iv) industry and market conditions in which the reporting unit operates, (v)
macroeconomic conditions, including discount rate changes, and (vi) changes in products or services offered by the reporting
F-13
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
unit. If applicable, performance in recent years was compared to forecasts included in prior valuations. Based on the results of
the qualitative assessment, the Company concluded that it was not more likely than not that the carrying values of the goodwill
and intangible assets were greater than their fair values, and that further quantitative testing was not necessary.
In the annual 2020 quantitative impairment assessment performed at the beginning of the fourth quarter, the Company
utilized a combination of income and market approaches to determine the fair value of two DD reporting units and an income
approach to determine the fair value of the Canadian reporting unit and its indefinite-lived assets consisting of acquired
Canadian licenses. Based upon the results of the quantitative assessments, the Company concluded that the fair values of the
goodwill and intangible assets, including the indefinite-lived Canadian licenses, as of October 1, 2020, were greater than the
carrying values.
Although the Company believes that the current assumptions and estimates used in its goodwill analysis are reasonable,
supportable, and appropriate, continued efforts to maintain or improve the performance of these businesses could be impacted
by unfavorable or unforeseen changes which could impact the existing assumptions used in the impairment analysis. Various
factors could reasonably be expected to unfavorably impact existing assumptions: primarily delays in new customer bookings
and the related delay in revenue from new customers, increases in customer termination activity or increases in operating costs.
In addition, given the ongoing and rapidly changing nature of the COVID-19 pandemic, there is significant uncertainty
regarding the duration and severity of the pandemic as well as any future government restrictions, which may unfavorably
impact existing assumptions. Accordingly, there can be no assurance that the estimates and assumptions made for the purposes
of the goodwill impairment analysis will prove to be accurate predictions of future performance.
Management's impairment analysis for certain reporting units utilized significant judgments and assumptions related to the
market comparable method analysis, such as selected market multiples, and related to cash flow projections, such as revenue
and terminal growth rates, projected operating margin, and the discount rate. A significant increase in the discount rate,
decrease in the revenue and terminal growth rate, or decreased operating margin, or substantial reductions in end markets and
volume assumptions could have a negative impact on the estimated fair value of this reporting unit. A future impairment charge
for goodwill or intangible assets could have a material effect on the Company's consolidated financial position and results of
operations.
Long-lived assets, other than goodwill and indefinite-lived assets, are reviewed for impairment whenever events or changes
in circumstances indicate that the carrying amounts may not be recoverable. Recoverability of assets to be held and used is
determined by the Company at the level for which there are identifiable cash flows by comparison of the carrying amount of the
assets to future undiscounted net cash flows before interest expense and income taxes expected to be generated by the assets.
Impairment, if any, is measured by the amount by which the carrying amount of the assets exceeds the fair value of the assets
(based on market prices in an active market or on discounted cash flows). Assets to be disposed of are reported at the lower of
the carrying amount or fair value.
Intangible Assets
Intangible assets are amortized on a straight-line basis over the expected periods to be benefited, as set forth in the table
below, such as legal life for patents and technology and contractual lives for non-compete agreements.
Customer relationships
Patents, licenses and technology
Non-compete agreements
Trade names
Debt Issuance Costs
Years
-
-
-
10
3
3
1
36
15
5
15
The costs related to the issuance of debt are capitalized, netted against the related debt for presentation purposes and
amortized to interest expense over the terms of the related debt.
Professional Liability
The Company is self-insured (up to certain limits) for professional liability claims arising in the normal course of business,
generally related to the testing and reporting of laboratory test results. The Company estimates a liability that represents the
ultimate exposure for aggregate losses below those limits. The liability is based on assumptions and factors for known and
incurred but not reported claims, including the frequency and payment trends of historical claims.
F-14
Index
Leases
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
On January 1, 2019 the Company adopted the new lease accounting standard using the modified retrospective method.
Comparative periods were not adjusted and are presented in accordance with the lease guidance in effect for that period. The
Company elected the package of practical expedients, which includes not reassessing whether existing contracts contain leases
under the new definition of a lease, reassessing the classification of existing leases, and reassessing whether previously
capitalized initial direct costs qualify for capitalization under the new standard. The new standard requires lessees to apply a
dual approach, classifying leases as either finance or operating leases based on the principle of whether or not the lease is
effectively a financed purchase by the lessee. The classification will determine whether lease expense is recognized based on an
effective interest method or on a straight-line basis over the term of the lease. A lessee is also required to record a right-of-use
(ROU) asset and a lease liability for all leases with a term of greater than 12 months regardless of their classification. The
Company elected to utilize the short-term lease exemption and not record leases with initial terms of 12 months or less on the
balance sheet. Leases with an initial term of 12 months or less are not recorded on the Consolidated Balance Sheets. Operating
lease expense is recognized on a straight-line basis over the lease term. Operating lease assets and liabilities are recognized at
the commencement date, based on the present value of the future lease payments over the lease term.
A certain number of these leases contain rent escalation clauses either fixed or adjusted periodically for inflation or market
rates that are factored into the Company's determination of lease payments. The Company also has variable lease payments that
do not depend on a rate or index, for items such as volume purchase commitments, which are recorded as variable cost when
incurred. As most of the Company's leases do not provide an implicit rate, the Company estimates an incremental borrowing
rate based on the credit quality of the Company and by comparing interest rates available in the market for similar borrowings,
and adjusting this amount based on the impact of collateral over the term of each lease. The Company uses this rate to discount
payments to present value. Some operating leases contain renewal options, some of which also include options to early
terminate the leases. The exercise of these options is at the Company's discretion. The Company determined that all renewal
options within leases for main laboratories, rapid response (STAT) laboratories, branches or combination sites were reasonably
possible to be exercised and therefore are included in the accounting lease term. See Note 5 Leases to the Consolidated
Financial Statements.
Income Taxes
The Company accounts for income taxes utilizing the asset and liability method. Under this method deferred tax assets and
liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying
amounts of existing assets and liabilities and their respective tax bases and for tax loss carryforwards. Deferred tax assets and
liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary
differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is
recognized in income in the period that includes the enactment date. The Company does not recognize a tax benefit unless the
Company concludes that it is more likely than not that the benefit will be sustained on audit by the taxing authority based solely
on the technical merits of the associated tax position. If the recognition threshold is met, the Company recognizes a tax benefit
measured at the largest amount of the tax benefit that the Company believes is greater than 50% likely to be realized. The
Company records interest and penalties in income tax expense.
Derivative Financial Instruments
Interest rate swap agreements, which have been used by the Company from time to time in the management of interest rate
exposure, are accounted for at fair value.
Cross currency swap agreements, which have been used by the Company to hedge exposure of its net investment in a
foreign subsidiary denominated in non-U.S. currency, are accounted for at fair value.
See Note 19 Derivative Instruments and Hedging Activities for the Company’s objectives in using derivative instruments
and the effect of derivative instruments and related hedged items on the Company’s financial position, financial performance
and cash flows.
Fair Value of Financial Instruments
Fair value measurements for financial assets and liabilities are determined based on the assumptions that a market
participant would use in pricing an asset or liability. A three-tiered fair value hierarchy draws distinctions between market
participant assumptions based on (i) observable inputs such as quoted prices in active markets (Level 1), (ii) inputs other than
quoted prices in active markets that are observable either directly or indirectly (Level 2) and (iii) unobservable inputs that
require the Company to use present value and other valuation techniques in the determination of fair value (Level 3).
F-15
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Research and Development
The Company expenses R&D costs as incurred.
Foreign Currencies
For subsidiaries outside of the U.S. that operate in a local currency environment, income and expense items are translated to
U.S. dollars at the monthly average rates of exchange prevailing during the period, assets and liabilities are translated at period-
end exchange rates and equity accounts are translated at historical exchange rates. Translation adjustments are accumulated in a
separate component of shareholders’ equity in the consolidated balance sheets and are included in the determination of
comprehensive income in the consolidated statements of comprehensive earnings and consolidated statements of changes in
shareholders’ equity. Transaction gains and losses are included in the determination of net income in the consolidated
statements of operations.
New Accounting Pronouncements
In August 2018, the FASB issued a new accounting standard to reduce, modify, and add to the disclosure requirements on
defined benefit pension and other postretirement plans. The standard is effective on January 1, 2021, with early adoption
permitted. The adoption of this standard is not expected to have a material impact on the consolidated financial statements.
In December 2019, the FASB issued a new accounting standard to simplify accounting for income taxes and remove,
modify, and add to the disclosure requirements of income taxes. The standard is effective January 1, 2021, with early adoption
permitted. The adoption of this standard is not expected to have a material impact on the consolidated financial statements.
In January 2020, the FASB issued a new accounting standard to clarify the interaction of the accounting for equity securities
and investments accounted for under the equity method of accounting and the accounting for certain forward contracts and
purchased options. The standard is effective January 1, 2021. The adoption of this standard is not expected to have a material
impact on the consolidated financial statements.
In March 2020, the FASB issued a new accounting standard to provide optional expedients and exceptions if certain
conditions are met for applying GAAP to contracts, hedging relationships, and other transactions affected by reference rate
reform. The expedients and exceptions in the standard are effective between March 12, 2020, and December 31, 2022. The
Company did not elect to apply any of the expedients or exceptions for the period ended December 31, 2020, and is currently
evaluating the impact this new standard will have on the consolidated financial statements.
In August 2020, the FASB issued a new accounting standard to address issues identified as a result of the complexity
associated with applying generally accepted accounting principles for convertible instruments and contracts in an entity's own
equity. The standard is effective January 1, 2022, with early adoption permitted. The Company is evaluating the impact this
new standard will have on the consolidated financial statements.
2. REVENUES
Description of Revenues
Dx attributes revenues to a geographical region based upon where the diagnostic test is performed, while DD attributes
revenues to a geographical region based upon where the services are performed. The Company's revenue by segment payers/
customer groups for the years ended December 31, 2020, 2019 and 2018 is as follows:
For the Year Ended
December 31, 2020
For the Year Ended
December 31, 2019
For the Year Ended
December 31, 2018
North
North
North
America Europe Other
Total
America Europe Other
Total
America Europe Other
Total
Payer/Customer
Dx
Clients
Patients
Medicare and Medicaid
Third-party
Total Dx revenues by payer
DD
Biopharmaceutical and
medical device companies
20 %
6 %
7 %
32 %
65 %
— %
— %
— %
— %
— %
— %
— %
— %
— %
— %
20 %
6 %
7 %
32 %
65 %
17 %
8 %
8 %
27 %
60 %
— %
— %
— %
— %
— %
— %
— %
— %
— %
— %
17 %
8 %
8 %
27 %
60 %
18 % — % — % 18 %
8 %
8 % — % — %
9 % — % — %
9 %
27 % — % — % 27 %
62 % — % — % 62 %
17 %
11 %
7 %
35 %
21 %
12 %
7 %
40 %
19 % 12 %
7 % 38 %
Total revenues
82 %
11 %
7 % 100 %
81 %
12 %
7 % 100 %
81 % 12 %
7 % 100 %
F-16
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Revenues in the U.S. were $11,192.3 (80.1%), $8,981.3 (77.7%) and $8,843.5 (78.0%) for the years ended December 31,
2020, 2019 and 2018.
The following is a description of the current revenue recognition policies of the Company:
Dx
Dx is an independent clinical laboratory business. It offers a comprehensive menu of frequently requested and specialty
diagnostic tests through an integrated network of primary and specialty laboratories across the U.S. In addition to diagnostic
testing along with occupational and wellness testing for employers and forensic DNA analysis, Dx also offered a range of other
testing services.
Within the Dx segment, a revenue transaction is initiated when Dx receives a requisition order to perform a diagnostic test.
The information provided on the requisition form is used to determine the party that will be billed for the testing performed and
the expected reimbursement. Dx recognizes revenue and satisfies its performance obligation for services rendered when the
testing process is complete and the associated results are reported. Sales are distributed among four payer portfolios - clients,
patients, Medicare and Medicaid and third-party. Dx considers negotiated discounts and anticipated adjustments, including
historical collection experience for the payer portfolio, when sales are recorded.
The following are descriptions of the Dx payer portfolios:
Clients
Client payers represent the portion of Dx’s revenue related to physicians, hospitals, health systems, accountable care
organizations (ACOs), employers and other entities where payment is received exclusively from the entity ordering the testing
service. Generally, client sales are recorded on a fee-for-service basis at Dx’s client list price, less any negotiated discount. A
portion of client billing is for laboratory management services, collection kits and other non-testing services or products. In
these cases, revenue is recognized when services are rendered or delivered.
Patients
This portfolio includes revenue from uninsured patients and member cost-share for insured patients (e.g., coinsurance,
deductibles and non-covered services). Uninsured patients are billed based upon Dx’s patient list fee schedules, net of any
discounts negotiated with physicians on behalf of their patients. Dx bills insured patients as directed by their health plan and
after consideration of the fees and terms associated with an established health plan contract.
Medicare and Medicaid
This portfolio relates to fee-for-service revenue from traditional Medicare and Medicaid programs. Revenue from these
programs is based on the fee schedule established by the related government authority. In addition to contractual discounts,
other adjustments including anticipated payer denials are considered when determining revenue. Any remaining adjustments to
revenue are recorded at the time of final collection and settlement. These adjustments are not material to Dx’s results of
operations in any period presented.
Third-Party
Third-party includes revenue related to MCOs. The majority of Dx's third-party revenue is reimbursed on a fee-for-service
basis. These payers are billed at Dx's established list price and revenue is recorded net of contractual discounts. The majority of
Dx’s MCO sales are recorded based upon contractually negotiated fee schedules with sales for non-contracted MCOs recorded
based on historical reimbursement experience.
In addition to contractual discounts, other adjustments including anticipated payer denials are considered when determining
revenue. Any remaining adjustments to revenue are recorded at the time of final collection and settlement. These adjustments
are not material to Dx’s results of operations in any period presented.
Third-party reimbursement is also received through capitation agreements with MCOs and independent physician
associations (IPAs). Under capitated agreements, revenue is recognized based on a negotiated per-member, per-month payment
for an agreed upon menu of tests, or based upon the proportionate share earned by Dx from a capitation pool. When the agreed
upon reimbursement is based solely on an established rate per member, revenue is not impacted by the volume of testing
performed. Under a capitation pool arrangement, the aggregate value of an established rate per member is distributed based on
the volume and complexity of the procedures performed by laboratories participating in the agreement. Dx recognizes revenue
monthly, based upon the established capitation rate or anticipated distribution from a capitated pool.
F-17
Index
DD
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
DD is a CRO business that provides end-to-end drug development services from early-stage research to clinical trial
management and beyond. DD provides these services predominantly to biopharmaceutical and medical device companies
worldwide. Because DD's client base generally consumes these drug development services across the entire portfolio of DD
pre-clinical and clinical services offerings, there is little variability in the customer base of any particular DD service offering.
The nature of DD’s obligations includes agreements to provide preclinical services, to manage a full clinical trial, provide
services for a specific phase of a trial, or provide research products to the customer. Generally, the amount of the transaction
price estimated at the beginning of the contract is equal to the amount expected to be billed to the customer. Other payments
may also factor into the calculation of transaction price, such as volume-based rebates that are retroactively applied to prior
transactions in the period.
Historically, a majority of DD’s revenues have been earned under contracts that range in duration from a few months to a
few years, but can extend in duration up to five years or longer. Occasionally, DD also has entered into minimum volume
arrangements with certain customers. Under these types of arrangements, if the annual minimum dollar value of a service
commitment is not reached, the customer is required to pay DD for the shortfall. Annual minimum commitment shortfalls are
not recognized until the end of the period when the amount has been determined and agreed to by the customer.
DD recognizes revenue either as services are performed or as products are delivered, depending on the nature of the work
contracted. If performance is completed at a specific point in time, the Company evaluates the nature of the agreement to
determine when the good or service is transferred into the customer’s control.
Service contracts generally take the form of fee-for-service or fixed-price arrangements subject to pricing adjustments based
on changes in scope. In cases where performance spans multiple accounting periods, revenue is recognized as services are
performed, measured on a proportional-performance basis, using either input or output methods that are specific to the service
provided. In an output method, revenue is determined by dividing the actual units of output achieved by the total units of output
required under the contract and multiplying that percentage by the total contract value. The total contract value, or total
contractual payments, represents the aggregate contracted price for each of the agreed upon services to be provided. When
using an input method, revenue is recognized by dividing the actual units of input incurred by the total units of input budgeted
in the contract, and multiplying that percentage by the total contract value. In each situation, the Company believes that the
methods used most accurately depict the progress of the Company towards completing its obligations. Billing schedules and
payment terms are generally negotiated on a contract-by-contract basis. In some cases, DD bills the customer for the total
contract value in progress-based installments as certain non-contingent billing milestones are reached over the contract
duration. These milestones include, but are not limited to, contract signing, initial dosing, investigator site initiation, patient
enrollment and/or database lock. The term “billing milestone” relates only to a billing trigger in a contract whereby amounts
become billable and payable in accordance with a negotiated predetermined billing schedule throughout the term of a project.
These billing milestones are generally not performance-based (i.e., there is no potential additional consideration tied to specific
deliverables or performance). In other cases, billing and payment terms are tied to the passage of time (e.g., monthly billings).
In either case, the total contract value and aggregate amounts billed to the customer would be the same at the end of the project.
Proportional performance contracts typically contain a single service (e.g., management of a clinical study) and therefore no
allocation of the contract price is required. Fee-for-service contracts are typically priced based on transaction volume. Since the
volume of activities in a fee-for-service contract is unspecified, the contract price is entirely variable and is allocated to the time
period in which it is earned. For contracts that include multiple distinct goods and services, DD allocates the contract price to
the goods and services based on a customer price list, if available. If a price list is not available, DD will estimate the
transaction price using either market prices or an “expected cost plus margin” approach.
While DD attempts to negotiate terms that provide for billing and payment of services prior or within close proximity to the
provision of services, this is not always possible. While a project is ongoing, cash payments are not necessarily representative
of aggregate revenue earned at any particular point in time, as revenues are recognized when services are provided, while
amounts billed and paid are in accordance with the negotiated billing and payment terms.
In some cases, payments received are in excess of revenue recognized. For example, a contract invoicing schedule may
provide for an upfront payment of 10% of the full contract value upon contract signing, but at the time of signing performance
of services has not yet begun. Payments received in advance of services being provided are deferred as contract liabilities on the
balance sheet. As the contracted services are subsequently performed and the associated revenue is recognized, the contract
liability balance is reduced by the amount of revenue recognized during the period.
In other cases, services may be provided and revenue recognized before the customer is invoiced. In these cases, revenue
recognized will exceed amounts billed, and the difference, representing a contract asset, is recorded for the amount that is
F-18
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
currently not billable to the customer pursuant to contractual terms. Once the customer is invoiced, the contract asset is reduced
for the amount billed, and a corresponding account receivable is recorded. All contract assets are billable to customers within
one year from the respective balance sheet date.
Most contracts are terminable with or without cause by the customer, either immediately or upon notice. These contracts
often require payment to DD of expenses to wind-down the study or project, fees earned to date and, in some cases, a
termination fee or a payment to DD of some portion of the fees or profits that could have been earned by DD under the contract
if it had not been terminated early. Termination fees are included in revenues when services are performed and realization is
assured.
The following are descriptions of the full range of drug development services provided by DD:
Preclinical services include fee-for-service activities such as bioanalytical testing services, and proportional performance
activities such as toxicology studies. Until June 3, 2019, preclinical services also included the sale of research models. See Note
3 Business Acquisitions and Dispositions to the Consolidated Financial Statements for more information. Revenue for sale of
research models was recognized at a point in time, typically upon shipment, when control transferred to the customer. Revenue
for bioanalytical testing services is recognized at a point in time upon communication of results to the customer. Revenue for
proportional performance activities, including toxicology studies, is recognized using an input-based measure of progress in
which revenue is recognized as expenses are incurred for the research models, labor hours, and other costs attributable to the
study.
Through its central laboratory, DD produces and supplies specimen collection kits that are utilized in clinical studies, and
provides transportation, project management, data management, and laboratory testing services on an as-needed basis
throughout the duration of its customers’ clinical studies. Revenue for central laboratory services is recognized using an output-
based measure of progress based on volume of activities in each period. DD also provides long-term specimen storage services,
for which revenue is recognized using an input-based measure of progress based on costs incurred.
DD provides clinical development and commercialization services, including clinical pharmacology services, full
management of Phase II through IV clinical studies, and market access solutions. Revenue for clinical pharmacology services,
which includes first-in-human trials, is recognized using an output-based measure of progress based on bed nights. Revenue for
full service clinical studies is recognized using an input-based measure of progress based on costs incurred (including pass-
through costs such as investigator grants and reimbursable out-of-pocket expenses). Revenue for market access solutions is
recognized using various methods. Revenue for fee-for-service arrangements, such as reimbursement consulting hotlines and
patient assistance programs, is recognized using an output method based on transaction volume which corresponds to the
amount charged to the customer. For consulting services billed based on time and materials, revenue is recognized using the
right to invoice practical expedient.
Contract costs
DD incurs sales commissions in the process of obtaining contracts with customers, which are recoverable through the
service fees in the contract. Sales commissions that are payable upon contract award are recognized as assets and amortized
over the expected contract term, along with related payroll tax expense. The amortization of commission expense is based on
the weighted average contract duration for all commissionable awards in the respective business in which the commission
expense is paid, which approximates the period over which goods and services are transferred to the customer. The amortization
period of sales commissions ranges from approximately 12-57 months, depending on the business. For businesses that enter
primarily short-term contracts, the Company applies the practical expedient which allows costs to obtain a contract to be
expensed when incurred if the amortization period of the assets that would otherwise have been recognized is one year or less.
Amortization of assets from sales commissions is included in selling, general, and administrative expense.
DD incurs costs to fulfill contracts with customers, which are recoverable through the service fees in the contract. Contract
fulfillment costs include software implementation costs and setup costs for certain market access solutions. These costs are
recognized as assets and amortized over the expected term of the contract to which the implementation relates, which is the
period over which services are expected to be provided to the customer. This period typically ranges from 24-60 months.
Amortization of deferred contract fulfillment costs is included in cost of goods sold.
Sales commission assets
Deferred contract fulfillment costs
Total
F-19
December 31, 2020 December 31, 2019
28.6
$
14.9
43.5
32.6 $
12.6
45.2 $
$
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Amortization related to sales commission assets and associated payroll taxes for the year ended December 31, 2020, 2019,
and 2018 was $23.2, $21.2 and $16.9, respectively. Amortization related to deferred contract fulfillment costs for the years
ended December 31, 2020, 2019 and 2018 was $10.1, $8.7 and $4.4, respectively. Impairment expense related to contract costs
was immaterial to the Company’s consolidated statement of operations. The Company applies the practical expedient to not
recognize the effect of financing in its contracts with customers, when the difference in timing of payment and performance is
one year or less.
Receivables, Unbilled Services and Unearned Revenue
Unbilled services are comprised primarily of unbilled receivables, but also include contract assets. A contract asset is
recorded when a right to payment has been earned for work performed, but billing and payment for that work is determined by
certain contractual milestones, whereas unbilled receivables are billable upon the passage of time. While DD attempts to
negotiate terms that provide for billing and payment of services prior or in close proximity to the provision of services, this is
not always possible and there are fluctuations in the level of unbilled services and unearned revenue from period to period. The
following table provides information about receivables, unbilled services, and unearned revenue (contract liabilities) from
contracts with customers for the DD segment:
Receivables, which are included in Accounts Receivable
Unbilled services
Unearned revenue
December 31, 2020 December 31, 2019
771.1
$
483.7
449.2
1,001.5 $
548.1
492.2
Revenue recognized during the period, that was included in the unearned revenue balance at the beginning of the period, for
the year ended December 31, 2020, and 2019, was $262.6 and $250.2, respectively.
Credit Loss Rollforward
With the adoption of the current expected credit loss standard in 2020, the Company estimates future expected losses on
accounts receivable, unbilled services and notes receivable over the remaining collection period of the instrument. The
rollforward for the allowance for credit losses for the year ended December 31, 2020, is as follows:
Year Ended December 31, 2020
Accounts
Receivable
Allowance for credit losses as of December 31, 2019
$
Current expected credit losses opening balance impact on retained earnings
Credit loss expense
Write offs
Ending allowance for credit losses
19.0 $
1.8
7.0
(5.7)
22.1 $
$
2.3 $
0.2
9.0
(0.2)
11.3 $
Unbilled
Services
Note and Other
Receivables
Total
— $ 21.3
7.0
5.0
16.7
0.7
(5.9)
—
5.7 $ 39.1
Notes and other receivables includes the $70.0 due 2022 from the Envigo transaction which is recorded in Other assets, net.
Performance Obligations Under Long-Term Contracts
Long-term contracts at the Company consist primarily of fully managed clinical studies within the DD segment. The amount
of existing performance obligations under such long-term contracts unsatisfied as of December 31, 2020, and 2019, was
$5,128.4 and $4,520.8, respectively. The Company expects to recognize approximately 26.0% of the remaining performance
obligations as of December 31, 2020, as revenue over the next 12 months, and the balance thereafter. The Company's long-term
contracts generally range from 1 to 8 years.
The Company applied the practical expedient and does not disclose information about remaining performance obligations
that have original expected durations of one year or less. The Company also did not disclose information about remaining
performance obligations when the variable consideration was related to a wholly unsatisfied performance obligation within a
series of obligations.
Within DD, revenue of $80.9 and $88.9 was recognized during the year ended December 31, 2020, and December 31, 2019,
respectively, from performance obligations that were satisfied in previous periods. This revenue comes from adjustments
related to changes in scope and estimates in full service clinical studies.
F-20
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
3. BUSINESS ACQUISITIONS AND DISPOSITIONS
During the year ended December 31, 2020, the Company acquired various businesses and related assets for approximately
$267.6 in cash (net of cash acquired). The purchase consideration for all acquisitions year to date has been allocated to the
estimated fair market value of the net assets acquired, including approximately $121.3 in identifiable intangible assets and a
residual amount of non-tax-deductible goodwill of approximately $166.2. The amortization periods for intangible assets
acquired from these businesses range from 12 to 15 years for customer relationships. These acquisitions were made primarily to
extend the Company's geographic reach in important market areas, enhance the Company's scientific differentiation and to
expand the breadth and scope of the Company's CRO services. The excess of the fair value of the consideration conveyed over
the fair value of the net assets acquired was recorded as goodwill. The goodwill reflects the Company's expectations to utilize
the acquired businesses’ workforce and established relationships and the benefits of being able to leverage operational
efficiencies with favorable growth opportunities in these markets. A summary of the net assets acquired in 2020 for these
businesses is included below:
Amounts Acquired During Year Ended
December 31, 2020
Accounts receivable
Unbilled services
Property, plant and equipment
Goodwill
Intangible assets
Total assets acquired
Accounts payable
Accrued expenses and other
Unearned revenue
Other liabilities
Total liabilities acquired
Net assets acquired
$
$
4.9
2.4
1.3
166.2
121.3
296.1
0.9
22.4
1.1
4.1
28.5
267.6
Unaudited Pro Forma Information for 2020 Acquisitions
Had the aggregate of the Company's 2020 acquisitions been completed as of January 1, 2019, the Company's pro forma
results would have been as follows:
Revenues
Net earnings attributable to Laboratory Corporation of America Holdings
2019
Years Ended December 31,
2020
2019
$
14,032.7 $
1,564.6
11,717.5
837.6
On June 3, 2019, the Company's DD segment acquired Envigo's nonclinical contract research services business, expanding
DD's global nonclinical drug development capabilities with additional locations and resources. Additionally, the Company
divested the CRP business, which was a part of the DD segment, to Envigo. As part of this sale, DD entered into a multi-year,
renewable supply agreement with Envigo. The Company paid cash consideration of $601.0, received a floating rate secured
note of $110.0, and recorded a loss on the sale of CRP of $12.2. The Company funded the transaction through the new term
loan facility entered into in 2019 concurrently with the transaction.
The final valuation of acquired assets and assumed liabilities as of June 3, 2019, include the following:
Consideration Transferred
Cash consideration
Fair value of CRP
Total
$
$
$
601.0
110.0
711.0
F-21
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Net Assets Acquired
Cash and cash equivalents
Accounts receivable
Unbilled services
Inventories
Prepaid expenses and other
Property, plant and equipment
Deferred income taxes
Goodwill
Customer relationships
Trade name and trademarks
Other assets
Total assets acquired
Accounts payable
Accrued expenses and other
Unearned revenue
Other liabilities
Total liabilities acquired
Net Envigo assets acquired
Floating rate secured note receivable due 2022
Total
Final
11.3
12.1
25.6
4.5
10.8
128.4
25.2
376.6
140.8
0.6
9.9
745.8
15.2
10.4
49.9
69.3
144.8
601.0
110.0
711.0
$
$
$
$
The purchase consideration for Envigo has been allocated to the estimated fair market value of the net assets acquired,
including approximately $141.4 in identifiable intangible assets and a residual amount of non-tax-deductible goodwill of
approximately $376.6. The amortization period for intangible assets acquired is 11 years for customer relationships.
The Envigo transaction contributed $124.2 and $17.9 of revenues and operating income, respectively, during the year ended
December 31, 2019. The divested CRP business contributed operating income of $5.5 and $13.2 for the years ended December
31, 2019 and 2018, respectively.
During the year ended December 31, 2019, in addition to the Envigo transaction, the Company acquired various businesses
and related assets for approximately $286.4 in cash (net of cash acquired). The purchase consideration for all acquisitions has
been allocated to the estimated fair market value of the net assets acquired, including approximately $184.3 in identifiable
intangible assets and a residual amount of non-tax-deductible goodwill of approximately $115.1. These acquisitions were made
primarily to extend the Company's geographic reach in important market areas, enhance the Company's scientific differentiation
and to expand the breadth and scope of the Company's CRO services. The excess of the fair value of the consideration
conveyed over the fair value of the net assets acquired was recorded as goodwill. The goodwill reflects the Company's
expectations to utilize the acquired businesses’ workforce and established relationships and the benefits of being able to
leverage operational efficiencies with favorable growth opportunities in these markets.
Unaudited Pro Forma Information for 2019 Acquisitions
Had the aggregate of the Company's 2019 acquisitions been completed as of January 1, 2018, the Company's pro forma
results would have been as follows:
Revenues
Net earnings attributable to Laboratory Corporation of America Holdings
2018
Years Ended December 31,
2019
2018
$
11,742.5 $
831.4
11,738.5
906.6
On April 30, 2018, the Company entered into a definitive agreement to sell the CFS business, a global provider of
innovative product design and product integrity services for end-user segments that span the global food supply chain, for an
all-cash purchase price of $670.0. The transaction closed on August 1, 2018, and a net gain of $258.3 was recorded in Other,
net in the consolidated statement of operations.
F-22
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
The Company also divested its forensic testing services business in the U.K. and the U.S. on August 7, 2018, and December
31, 2018, respectively, resulting in losses of $48.9 and $24.5, respectively, recorded in Other, net in the consolidated statement
of operations.
Operating income for the Company's businesses divested in 2018 was $7.6 for the year ended December 31, 2018, (which
includes divested operations through their respective disposal dates).
4. RESTRUCTURING AND OTHER CHARGES
During 2020, the Company recorded net restructuring charges of $40.6; $15.3 within Dx and $25.3 within DD. The charges
were comprised of $14.1 in severance and other personnel costs $17.4 for facility, operating lease right-of-use and equipment
impairments, and $18.9 in facility closures and general integration activities. The charges were offset by the reversal of
previously established liability of $0.6 and $9.2 in unused severance costs and facility-related costs, respectively.
During 2019, the Company recorded net restructuring charges of $54.6; $26.7 within Dx and $27.9 within DD. The charges
were comprised of $32.9 in severance and other personnel costs and $24.9 in facility-related costs primarily associated with
general integration activities. The charges were offset by the reversal of previously established liability of $1.7 in unused
severance and $1.5 in unused facility-related costs.
During 2018, the Company recorded net restructuring charges of $48.1; $20.5 within Dx and $27.6 within DD. The charges
were comprised of $40.3 in severance and other personnel costs, $11.8 in facility-related costs primarily associated with general
integration activities. The charges were offset by the reversal of previously established liability of $2.0 in unused severance and
$2.0 in unused facility-related costs. The Company also recorded $2.3 in impairment to land held for sale which is included in
amortization expense.
The following represents the Company’s restructuring activities for the period indicated:
Dx
DD
Balance as of December 31, 2018
Reclassification for ASC 842 adoption
Restructuring charges
Impairment of facility related assets
Reduction of prior restructure accruals
Cash payments and other adjustments
Balance as of December 31, 2019
Restructuring charges
Impairment of facility related assets
Reduction of prior restructuring accruals
Cash payments and other adjustments
Balance as of December 31, 2020
Current
Non-current
Severance and
Other
Employee Costs
2.1
$
—
17.3
—
(0.2)
(18.7)
0.5
5.2
—
(0.1)
(5.3)
0.3
$
$
$
$
Lease and
Other
Facility Costs
$
Severance and
Other
Employee Costs
Lease and
Other
Facility Costs
Total
7.4 $
(5.7)
(1.8)
11.8
(0.4)
(8.6)
2.7 $
5.5
7.5
(2.8)
(12.5)
0.4 $
6.5 $
—
15.6
—
(1.5)
(15.1)
5.5 $
8.9
—
(0.5)
(11.5)
2.4 $
27.6 $ 43.6
(32.8)
(27.1)
33.1
2.0
24.7
12.9
(3.2)
(1.1)
(52.0)
(9.6)
13.4
4.7
33.0
13.4
17.4
9.9
(9.8)
(6.4)
(46.2)
(16.9)
7.8
4.7 $
5.7
$
2.1
7.8
$
The non-current portion of the restructuring liabilities is expected to be paid out over 4.9 years. Cash payments and other
adjustments include the reclassification of profit sharing, pension, and holiday accrual.
5. LEASES
The Company has operating and finance leases for patient service centers, laboratories and testing facilities, clinical
facilities, general office spaces, vehicles, and office and laboratory equipment. Leases have remaining lease terms of less than a
year to 13 years, some of which include options to extend the leases for up to 15 years.
F-23
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
The components of lease expense were as follows:
Operating lease cost
Finance lease cost:
Amortization of right-of-use assets
Interest on lease liabilities
Total finance lease cost
Supplemental cash flow information related to leases was as follows:
Cash paid for amounts included in the measurement of lease liabilities:
Operating cash flows from operating leases
Operating cash flows from finance leases
Financing cash flows from finance leases
ROU assets obtained in exchange for lease obligations:
Operating leases
Finance leases
Supplemental balance sheet information related to leases was as follows:
Operating Leases
Operating lease ROU assets (included in Property, plant and equipment, net)
Short-term operating lease liabilities
Operating lease liabilities
Total operating lease liabilities
Finance Leases
Finance lease ROU assets (included in Other assets)
Short-term finance lease liabilities
Financing lease liabilities
Total finance lease liabilities
Weighted Average Remaining Lease Term
Operating leases
Finance leases
Weighted Average Discount Rate
Operating leases
Finance leases
Maturities of lease liabilities are as follows:
Year Ended December 31, 2020
2021
2022
2023
2024
2025
Thereafter
Total lease payments
Less imputed interest
Less current portion
Total maturities, due beyond one year
F-24
For the Year Ended
December 31, 2020 December 31, 2019
224.0
$
215.4 $
$
$
11.2 $
4.7
15.9 $
11.1
6.7
17.8
For the Year Ended
December 31, 2020
December 31, 2019
$
$
(213.8) $
(4.7)
(15.2)
185.9 $
—
(227.3)
(6.7)
(8.9)
132.6
0.2
December 31, 2020 December 31, 2019
$
$
$
$
789.8
$
192.0
677.6
869.6
79.7
6.7
84.4
91.1
$
$
$
7.6
15.9
3.3 %
5.1 %
732.8
206.5
596.6
803.1
87.7
8.4
91.1
99.5
7.6
15.5
4.1 %
5.2 %
Operating Leases
Finance Leases
$
$
$
206.1 $
162.9
119.8
85.8
71.5
354.8
1,000.9 $
(131.3)
(192.0)
677.6 $
12.7
11.6
11.4
10.5
7.7
89.2
143.1
(52.0)
(6.7)
84.4
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Rent expense for short term leases with a term less than one year for the years ended December 31, 2020 and 2019
amounted to $6.8 and $10.6, respectively. The Company has variable lease payments that do not depend on a rate index,
primarily for purchase volume commitments, which are recorded as variable cost when incurred. Total variable payments for
the year ended December 31, 2020 and 2019 were $26.7 and $20.8. As of December 31, 2020, the Company has entered into
two additional operating leases, for patient service centers that have not yet commenced and are not significant to the overall
lease portfolio. These operating leases will commence in 2021 with lease terms of three years. Rent expense, which includes
rent for real estate, equipment and automobiles under operating leases under ASC 840 amounted to $358.7 for the year ended
December 31, 2018.
6. JOINT VENTURE PARTNERSHIPS AND EQUITY METHOD INVESTMENTS
At December 31, 2020, the Company had investments in the following unconsolidated joint venture partnerships and equity
method investments:
Locations
Joint Venture Partnerships:
Alberta, Canada (2)
Florence, South Carolina
Buffalo, New York
Equity Method Investments:
Various
Net Investment
Interest Owned
$
34.6
10.2
13.4
7.2
43.37 %
49.00 %
48.18 %
various
The joint venture partnerships are governed by agreements that mandate unanimous agreement between partners on all
major business decisions as well as providing other participating rights to each partner. The equity method investments
represent the Company’s purchase of ownership interests in clinical diagnostic companies. The investments are accounted for
under the equity method of accounting as the Company does not have control of these investments. The Company has no
material obligations or guarantees to, or in support of, these unconsolidated investments and their operations.
The Company’s investment in one of its Alberta joint venture partnerships at December 31, 2020, includes $22.4 of value
assigned to that partnership’s Canadian license to conduct diagnostic testing services in the province. Substantially all of the
joint venture's revenue is received as reimbursement from the Alberta government's healthcare programs (AHS). While the
Canadian license provides the joint venture the ability to conduct diagnostic testing in Alberta, it does not guarantee that the
provincial government will continue to reimburse diagnostic laboratory testing in future years at current levels. A decision by
the provincial government to limit or reduce its reimbursement of laboratory diagnostic services would have a negative impact
on the profits and cash flows the Company derives from the joint venture. In August 2016, AHS and the Canadian partnership
reached an agreement to extend the contract for five additional years through March 2022, with the intent to have the services
provided pursuant to the contract transferred to AHS at the end of the five-year period. In consideration of AHS acquiring the
assets and assuming liabilities in accordance with the parties’ agreement, AHS will pay CAD 50.0 to the partnership when the
transfer is effective, subject to a working capital adjustment. The Company is amortizing the value of the partnership's
Canadian license to its residual value over the remaining term of the agreement. In December 2019, AHS issued a Request for
Expression of Interest, that seeks to gauge market interest from private third parties for the provision of community lab services
in Alberta. The Canadian partnership submitted a response indicating its interest in providing lab services.
7. ACCOUNTS RECEIVABLE
Dx accounts receivable
DD accounts receivable
Less DD allowance for doubtful accounts
Accounts receivable
December 31,
2020
December 31,
2019
$
$
1,515.5 $
986.4
(22.1)
2,479.8 $
798.1
764.8
(19.0)
1,543.9
F-25
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
8. PROPERTY, PLANT AND EQUIPMENT, NET
Land
Buildings and building improvements
Machinery and equipment
Software
Leasehold improvements
Furniture and fixtures
Construction in progress
Operating lease ROU assets
Less accumulated depreciation
December 31,
2020
December 31,
2019
$
$
99.4 $
879.9
1,522.3
857.5
440.0
112.2
231.6
789.8
4,932.7
(2,203.1)
2,729.6 $
90.9
781.8
1,345.1
794.9
411.7
97.0
311.1
732.8
4,565.3
(1,928.7)
2,636.6
Depreciation expense and amortization of property, plant and equipment was $349.3, $321.5 and $311.5 for 2020, 2019 and
2018, respectively, including software depreciation of $84.7, $90.4, and $92.7 for 2020, 2019 and 2018, respectively.
9. GOODWILL AND INTANGIBLE ASSETS
The changes in the carrying amount of goodwill (net of accumulated amortization) for the years ended December 31, 2020
and 2019 are as follows:
Dx
DD
Total
December 31,
2020
December 31,
2019
December 31,
2020
December 31,
2019
December 31,
2020
December 31,
2019
Balance as of January 1
Goodwill acquired during the year
Dispositions
Impairment
Foreign currency impact and other
adjustments to goodwill
Balance at end of year
$ 3,721.5 $ 3,638.8 $ 4,143.5 $ 3,721.5 $ 7,865.0 $ 7,360.3
494.5
(12.6)
414.3
(12.6)
166.2
—
80.2
—
90.4
—
75.8
—
(3.7)
—
(418.7)
—
(422.4)
—
6.6
22.8
$ 3,800.2 $ 3,721.5 $ 3,951.3 $ 4,143.5 $ 7,751.5 $ 7,865.0
142.7
136.1
20.3
2.5
The components of identifiable intangible assets are as follows:
Customer relationships
Patents, licenses and technology
Non-compete agreements
Trade names
Land use rights
Canadian licenses
December 31, 2020
December 31, 2019
Gross
Carrying
Amount
Accumulated
Amortization
Net
Carrying
Amount
Gross
Carrying
Amount
Accumulated
Amortization
Net
Carrying
Amount
$
$
4,643.3 $
434.7
109.6
401.8
10.9
489.8
6,090.1 $
(1,534.9) $
(252.6)
(70.7)
(263.9)
(6.9)
—
(2,129.0) $
3,108.4 $
182.1
38.9
137.9
4.0
489.8
3,961.1 $
4,441.7 $
453.6
90.9
408.2
10.9
480.3
5,885.6 $
(1,329.5) $
(235.7)
(60.5)
(219.9)
(5.5)
—
(1,851.1) $
3,112.2
217.9
30.4
188.3
5.4
480.3
4,034.5
During 2020, the Company recorded goodwill and other asset impairment charges of $462.1, $450.5 within DD and $11.6
within Dx. The Company concluded that the fair value was less than the carrying value for two of its reporting units and
recorded goodwill impairment of $418.7 and $3.7 for DD and Dx, respectively. Additional impairment of identifiable intangible
and tangible assets of $31.8 and $7.9 was recorded for DD and Dx, respectively, for impairment of a tradename, software,
customer relationships, and technology assets.
As part of the rebranding initiative, the Company reduced the estimated useful life of its trade name assets to reflect their
anticipated use through December 2021. This change in estimated useful life resulted in accelerated amortization of $27.5 in
2020.
F-26
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
A summary of amortizable intangible assets acquired during 2020, and their respective weighted average amortization
periods are as follows:
Customer relationships
Trade name
Non-compete agreements
Amount
$
$
102.4
0.2
18.7
121.3
Weighted Average
Amortization Period
14.1
2.4
5.0
12.7
Amortization of intangible assets, including amortization of the Canadian license recorded in other assets, was $275.4, $243.2
and $231.7 in 2020, 2019 and 2018, respectively. The Company recorded purchase accounting adjustments and impairment
losses through amortization expense of $0.0, $0.4, and $4.5 in 2020, 2019 and 2018, respectively. Amortization expense of
intangible assets is estimated to be $365.5 in fiscal 2021, $220.8 in fiscal 2022, $217.8 in fiscal 2023, $213.2 in fiscal 2024,
$200.8 in fiscal 2025, and $2,160.5 thereafter.
10. ACCRUED EXPENSES AND OTHER
Employee compensation and benefits
Accrued taxes payable
Other
11. OTHER LIABILITIES
Defined-benefit plan obligation
Deferred compensation plan obligation
Other
12. DEBT
December 31, 2020 December 31, 2019
474.6
$
156.7
311.1
942.4
623.2 $
374.8
359.7
1,357.7 $
$
December 31, 2020 December 31, 2019
188.4
$
76.7
118.1
383.2
220.5 $
89.2
216.7
526.4 $
$
Short-term borrowings and current portion of long-term debt at December 31, 2020, and 2019 consisted of the following:
4.625% senior notes due 2020
2019 term loan
Debt issuance costs
Current portion of note payable
Total short-term borrowings and current portion of long-term debt
Long-term debt at December 31, 2020, and 2019 consisted of the following:
3.75% senior notes due 2022
3.20% senior notes due 2022
4.00% senior notes due 2023
3.25% senior notes due 2024
3.60% senior notes due 2025
3.60% senior notes due 2027
4.70% senior notes due 2045
2.30% senior notes due 2024
2.95% senior notes due 2029
2019 term loan
Debt issuance costs
Note payable
Total long-term debt
F-27
—
375.0
December 31, 2020 December 31, 2019
413.7
—
(0.7)
2.2
415.2
(0.4)
2.1
376.7 $
$
December 31, 2020 December 31, 2019
500.0
500.0
300.0
600.0
1,000.0
600.0
900.0
400.0
650.0
375.0
(42.2)
7.0
5,789.8
500.0
500.0
300.0
600.0
1,000.0
600.0
900.0
400.0
650.0
—
(37.1)
6.1
5,419.0 $
$
Index
Credit Facilities
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
On June 3, 2019, the Company entered into a new $850.0 term loan (the 2019 Term Loan). The 2019 Term Loan will
mature on June 3, 2021. Proceeds of the 2019 Term Loan were used to repay approximately $250.0 of the 2017 Term Loan and
to fund the acquisition of Envigo's nonclinical research services business.
The 2019 Term Loan accrues interest at a per annum rate equal to, at the Company's election, either a LIBOR rate plus a
margin ranging from 0.55% to 1.175%, or a base rate determined according to a prime rate or federal funds rate plus a margin
ranging from 0.0% to 0.175%. As of December 31, 2020, the effective interest rate on the 2019 Term Loan was 0.95%.
On September 15, 2017, the Company entered into a $750.0 term loan (the 2017 Term Loan). The 2017 Term Loan accrued
interest at a per annum rate equal to, at the Company's election, either a LIBOR rate plus a margin ranging from 0.875% to
1.50%, or a base rate determined according to a prime rate or federal funds rate plus a margin ranging from 0.0% to 0.50%. The
2017 Term Loan was fully repaid in 2019.
The Company also maintains a senior revolving credit facility consists of a five-year revolving facility in the principal
amount of up to $1,000.0, with the option of increasing the facility by up to an additional $350.0, subject to the agreement of
one or more new or existing lenders to provide such additional amounts and certain other customary conditions. The revolving
credit facility also provides for a subfacility of up to $100.0 for swing line borrowings and a subfacility of up to $80.0 for
issuances of letters of credit. The Company is required to pay a facility fee on the aggregate commitments under the revolving
credit facility, at a per annum rate ranging from 0.10% to 0.25%. The revolving credit facility is permitted to be used for
general corporate purposes, including working capital, capital expenditures, funding of share repurchases and certain other
payments, acquisitions, and other investments. There were no balances outstanding on the Company's current revolving credit
facility at December 31, 2020, or December 31, 2019. As of December 31, 2020, the effective interest rate on the revolving
credit facility was 1.12%. The credit facility expires on September 15, 2022.
Under the Company's term loan facilities and the revolving credit facility, the Company is subject to negative covenants
limiting subsidiary indebtedness and certain other covenants typical for investment grade-rated borrowers and the Company is
required to maintain certain leverage ratios. The Company was in compliance with all covenants in its term loans and the
revolving credit facility at December 31, 2020, and December 31, 2019. In May 2020, in order to obtain increased financial
covenant flexibility, the Company and its lenders entered into amendments to the term loan facility and the revolving credit
facility to increase the maximum leverage ratio to 5.0x debt to last twelve months EBITDA for the three month periods ending
June 30, September 30 and December 31, 2020, and 4.5x for the period ended March 31, 2021. From and including the period
ending June 30, 2021, the maximum leverage ratio reverts back to 4.0x. The amendments also provide that during any period in
which the Company's leverage ratio exceeds 4.5x debt to last twelve months EBITDA (i) the Company will be prohibited from
consummating share repurchases, subject to limited exceptions, (ii) borrowings under the revolving credit facility will accrue
interest at a per annum rate equal to, at the Company's election, either a LIBOR rate plus a margin of 1.25% or a base rate plus
a margin of 0.25%, (iii) the facility fee that the Company is required to pay on the aggregate commitments under the revolving
credit facility will be 0.25% per annum, and (iv) borrowings under the term loan facility will accrue interest at a per annum rate
equal to, at the Company's election, either a LIBOR rate plus a margin of 1.175% or a base rate plus a margin of 0.175%. The
Company's leverage ratio did not exceed 4.5x debt to last twelve months EBITDA as of December 31, 2020.
The Company’s availability of $997.0 at December 31, 2020, under its revolving credit facility is reduced by the amount of
the Company's outstanding letters of credit.
Zero-Coupon Convertible Subordinated Notes
During 2019, the Company settled notices to convert $8.6 aggregate principal amount at maturity of its zero-coupon
subordinated notes with a conversion value of $16.6. The total cash used for these settlements was $8.2 and the Company also
issued 0.1 additional shares of common stock. As a result of these conversions in 2019, the Company also reversed
approximately $2.0 of deferred tax liability to reflect the tax benefit realized upon issuance of the shares. On December 19,
2019, the Company redeemed all remaining outstanding zero-coupon notes that had not previously converted.
Senior Notes
On August 17, 2020 the Company redeemed the remaining $412.2 of its 4.625% Senior Notes due November 15, 2020,
using available cash on hand. The Company exited the remaining fixed-to-variable interest rate swap agreement in August
2020, in connection with this redemption and recorded a gain of $1.6 on the extinguishment. The gain was included in Other,
net on the Consolidated Statement of Operations.
F-28
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
On November 25, 2019, the Company issued $1,050.0 in debt securities, consisting of $400.0 aggregate principal amount of
2.300% Senior Notes due 2024 and $650.0 aggregate principal amount of 2.950% Senior Notes due 2029. The net proceeds
from the new Senior Notes were used to redeem of all of the outstanding $500.0 principal amount of its 2.625% Senior Notes
due February 1, 2020, redeem $187.9 of the outstanding 4.625% Senior Notes due November 15, 2020 in a tender offer, and to
repay $348.3 outstanding under the Company's term loan credit facilities. The Company recorded a loss of $4.0 on the
extinguishment of the 2.625% Senior Notes and part of the outstanding 4.625% Senior Notes.
The scheduled payments of long-term debt at the end of 2020 are summarized as follows:
2021
2022
2023
2024
2025
Thereafter
Total scheduled payments
Less long-term debt issuance costs
Total long-term debt
Less current portion
Long-term debt, due beyond one year
$
$
376.7
1,000.0
300.0
1,000.0
1,000.0
2,156.1
5,832.8
(37.1)
5,795.7
(376.7)
5,419.0
13. PREFERRED STOCK AND COMMON SHAREHOLDERS’ EQUITY
The Company is authorized to issue up to 265.0 shares of common stock, par value $0.10 per share. The Company is
authorized to issue up to 30.0 shares of preferred stock, par value $0.10 per share. There were no preferred shares outstanding
as of December 31, 2020 and 2019.
The changes in common shares issued and held in treasury are summarized below:
Common Shares Issued
Common stock issued at January 1
Common stock issued under employee stock plans
Common stock issued upon conversion of zero-coupon subordinated notes
Retirement of treasury stock
Purchase of common stock
Common stock issued at December 31
Common Shares Held in Treasury
Common shares held in treasury at January 1
Surrender of restricted stock and performance share awards
Retirement of treasury shares
Common shares held in treasury at December 31
2020
2019
2018
97.2
0.9
—
—
(0.6)
97.5
122.4
1.2
0.1
(23.6)
(2.9)
97.2
125.1
1.6
—
—
(4.3)
122.4
2020
2019
2018
—
—
—
—
23.5
0.1
(23.6)
—
23.2
0.3
—
23.5
The Company’s treasury shares are recorded at aggregate cost. During 2019, the board of directors approved the retirement
of all current treasury shares and future shares received in settlement of tax liabilities related to restricted stock vesting.
Share Repurchase Program
During 2020, the Company purchased 0.6 shares of its common stock at an average price of $178.85 for a total cost
of $100.0. When the Company repurchases shares for retirement, the amount paid to repurchase the shares in excess of the par
or stated value is allocated to additional paid-in capital unless subject to limitation or the balance in additional paid-in-capital is
exhausted. Remaining amounts are recognized as a reduction in retained earnings. At the end of 2020, the Company had
outstanding authorization from its board of directors to purchase $800.0 of Company common stock. The repurchase
authorization has no expiration date. The Company reinstated its share repurchase program in October 2020 following the
temporary suspension of stock repurchases beginning in March 2020 due to the COVID-19 pandemic.
F-29
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Accumulated Other Comprehensive Earnings
The components of accumulated other comprehensive earnings are as follows:
Foreign
Currency
Translation
Adjustments
$
Net
Benefit
Plan
Adjustments
Accumulated
Other
Comprehensive
Earnings
Balance at December 31, 2018
Current year adjustments
Amounts reclassified from accumulated other comprehensive earnings (a)
Tax effect of adjustments
Balance at December 31, 2019
Current year adjustments
Amounts reclassified from accumulated other comprehensive earnings (a)
Tax effect of adjustments
Balance at December 31, 2020
$
(389.8) $
104.4
—
—
(285.4)
264.1
—
—
(21.3) $
(73.3) $
(22.5)
5.1
3.7
(87.0)
(72.9)
7.2
12.1
(140.6) $
(463.1)
81.9
5.1
3.7
(372.4)
191.2
7.2
12.1
(161.9)
(a) The amortization of prior service cost is included in the computation of net periodic benefit cost. Refer to Note 17 Pension
and Postretirement Plans for additional information regarding the Company's net periodic benefit cost.
14. INCOME TAXES
The sources of income before taxes, classified between domestic and foreign entities are as follows:
Domestic
Foreign
Total pre-tax income
2020
1,846.5 $
372.5
2,219.1 $
$
$
2019
784.4 $
320.5
1,104.9 $
2018
937.7
330.6
1,268.3
The provisions (benefits) for income taxes in the accompanying consolidated statements of operations consist of the
following:
Current:
Federal
State
Foreign
Deferred:
Federal
State
Foreign
Years Ended December 31,
2019
2018
2020
$
$
$
$
455.3 $
172.8
81.0
709.1 $
(6.7) $
(28.1)
(12.2)
(47.0)
662.1 $
126.7 $
40.2
83.9
250.8 $
38.2 $
2.5
(11.5)
29.2
280.0 $
225.8
61.2
64.3
351.3
(2.5)
30.0
5.6
33.1
384.4
F-30
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
The effective tax rates on earnings before income taxes are reconciled to statutory U.S. income tax rates as follows:
Years Ended December 31,
2019
2018
2020
Statutory U.S. rate
State and local income taxes, net of U.S. Federal income tax effect
Foreign earnings taxed at lower rates than the statutory U.S. rate
Restructuring and acquisition items
Re-measurement of deferred taxes
Repatriation tax
Impairment of assets
GILTI
Other
Effective rate
21.0 %
5.3
(0.4)
—
—
—
4.0
(0.1)
—
29.8 %
21.0 %
3.2
(0.1)
0.7
—
—
—
1.1
(0.6)
25.3 %
21.0 %
3.4
(0.3)
1.9
2.4
1.2
—
1.0
(0.3)
30.3 %
On December 22, 2017, the U.S. Securities and Exchange Commission (SEC) issued Staff Accounting Bulletin No. 118
(SAB 118), which allowed companies one year to finalize the tax accounting for the 2017 enacted Tax Cuts and Jobs Act
(TCJA) in its financial statements. Under SAB 118, in 2018 the Company recorded a total tax expense of $45.0, $14.8 related to
the TCJA repatriation tax and $30.1 for the remeasurement of deferred taxes.
The TCJA includes provisions relating to global low-taxed intangible income (GILTI). The Company finalized its decision
on accounting policy during the fourth quarter of 2018. The Company will account for GILTI as a periodic charge in the period
it arises.
The tax effects of temporary differences that give rise to significant portions of the deferred tax assets and deferred tax
liabilities are as follows:
Deferred tax assets:
Accounts receivable
Employee compensation and benefits
Operating lease liability
Acquisition and restructuring reserves
Tax loss carryforwards
Other
Less: valuation allowance
Deferred tax assets, net of valuation allowance
Deferred tax liabilities:
Right of use asset
Intangible assets
Property, plant and equipment
Other
Total gross deferred tax liabilities
Net deferred tax liabilities
The table below provides a rollforward of the valuation allowance.
December 31, 2020
December 31, 2019
$
$
$
$
20.0 $
115.6
187.6
22.6
206.8
126.8
679.4
(167.6)
511.8 $
(179.5) $
(912.5)
(203.9)
(46.3)
(1,342.2)
(830.4) $
16.9
105.1
191.4
9.9
207.1
62.9
593.3
(145.4)
447.9
(177.3)
(910.5)
(194.6)
(57.4)
(1,339.8)
(891.9)
Beginning balance
Additions charged to expense
Reductions and other adjustments
Ending balance
December 31, 2020
$
December 31, 2019
145.4 $
5.8
16.4
167.6 $
$
156.9 $
—
(11.5)
145.4 $
December 31, 2018
153.5
3.4
—
156.9
The Company has U.S. federal tax loss carryforwards of approximately $185.2, which expire periodically through 2036, as
well as post 2017 carryovers of $0.1 that are limited to 80% of taxable income and have an indefinite carryover. The utilization
of tax loss carryforwards is limited due to change of ownership rules; however, at this time, the Company expects to fully
utilize substantially all U.S. federal tax loss carryforwards with the exception of approximately $3.9 for which a full valuation
F-31
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
allowance has been provided. The Company has U.S. state tax loss carryforwards of $540.3, which also expire periodically
through 2038, and on which a valuation allowance of $340.0 has been provided. In addition to federal and state tax loss
carryforwards, the Company has other federal and state attribute carry forwards of $288.6. These attribute carryforwards have
indefinite lives and a valuation allowance of $229.6. The Company has foreign tax loss carryforwards of $59.1 which have an
indefinite life and on which a valuation allowance of $25.9 has been provided, as well as foreign tax loss carryforwards of
$502.9 which expire periodically through 2034 that have a full valuation allowance. In addition to the foreign net operating
losses, the Company has a foreign capital loss carryforward of $6.9. The foreign capital loss carryforward has an indefinite life
and has a full valuation allowance.
The valuation allowance increased from $145.4 in 2019 to $167.6 in 2020 primarily due to capital loss disallowances
during the year that are not expected to be realized for tax purposes and for Swiss net operating losses not expected to be
realized as a result of the finalization of the Envigo acquisition.
Unrecognized income tax benefits were $48.8 and $31.7 at December 31, 2020, and 2019, respectively. It is anticipated that
the amount of the unrecognized income tax benefits will change within the next 12 months; however, these changes are not
expected to have a significant impact on the results of operations, cash flows or the financial position of the Company.
The Company recognizes interest and penalties related to unrecognized income tax benefits in income tax expense. Accrued
interest and penalties related to uncertain tax positions totaled $8.3 and $5.5 as of December 31, 2020, and 2019, respectively.
During the years ended December 31, 2020, 2019 and 2018, the Company recognized $4.4, $2.0 and $1.8, respectively, in
interest and penalties expense, which was offset by a benefit from reversing previous accruals for interest and penalties of $3.0,
$5.8 and $0.5, respectively. As of December 31, 2020 and 2019 interest expense of $1.4, and $0.8, respectively, was added to
accrued interest from the opening balance sheet of an acquisition.
The following table shows a reconciliation of the unrecognized income tax benefits, excluding interest and penalties, from
uncertain tax positions for the years ended December 31, 2020, 2019 and 2018:
Balance as of January 1
Increase in reserve for tax positions taken in the current year
Increase in reserve from an acquisition's opening balance sheet
Decrease in reserve as a result of payments
Decrease in reserve as a result of lapses in the statute of limitations
Balance as of December 31
2020
2019
2018
31.7 $
17.3
8.2
(0.3)
(8.1)
48.8 $
18.0 $
10.3
8.4
(0.8)
(4.2)
31.7 $
19.5
3.1
—
(4.6)
—
18.0
$
$
Also included in the balance of unrecognized tax benefits as of December 31, 2020, 2019 and 2018, are $2.1, $0.0 and
$0.0, respectively, of tax benefits that, if recognized, would result in adjustments to other tax accounts, primarily deferred taxes.
As of December 31, 2020, 2019 and 2018 there are $46.7, $31.7 and $18.0, respectively, of tax benefits that, if recognized
would favorably affect the effective income tax rate.
The Company has substantially concluded all U.S. federal income tax matters for years through 2016. Substantially all
material state and local and foreign income tax matters have been concluded through 2014 and 2010, respectively.
The Company is appealing a Canada Revenue Agency assessment related to the 2014 income tax return. The Company
believes adequate reserves have been established for the assessment. The Company has various state and foreign income tax
examinations ongoing throughout the year. The Company believes adequate provisions have been recorded related to all open
tax years.
As a result of the TCJA, the Company was effectively taxed on all of its previously unremitted foreign earnings. The TCJA
also enacts a territorial tax system that allows, for the most part, tax-free repatriation of foreign earnings. The Company still
considers the earnings of its foreign subsidiaries to be permanently reinvested, but if repatriation were to occur the Company
would be required to accrue U.S. taxes, if any, and remit applicable withholding taxes as appropriate. The Company has
unremitted earnings and profits of $702.4 and $601.4 that are permanently reinvested in its foreign subsidiaries as of
December 31, 2020, and 2019, respectively. A determination of the amount of the unrecognized deferred tax liability related to
these undistributed earnings is not practicable due to the complexity and variety of assumptions necessary based on the manner
in which the undistributed earnings would be repatriated.
F-32
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
15. STOCK COMPENSATION PLANS
Stock Incentive Plans
In 2016, the shareholders approved the Laboratory Corporation of America Holdings 2016 Omnibus Incentive Plan (the
Plan). Under the Plan, as of December 31, 2020, there are 9.4 shares authorized for issuance and 5.4 shares available for grant.
Stock Options
The following table summarizes grants of non-qualified options made by the Company to officers, key employees, and non-
employee directors under all plans. Stock options are generally granted at an exercise price equal to or greater than the fair
market price per share on the date of grant. Also, for each grant, options vest ratably over a period of three years on the
anniversaries of the grant date, and have a contractual exercise period of 10 years subject to their earlier expiration or
termination.
Changes in options outstanding under the plans for the period indicated were as follows:
Number of
Options
Weighted-Average
Exercise Price
per Option
Weighted-Average
Remaining
Contractual Term
Aggregate
Intrinsic
Value
Outstanding at December 31, 2019
Granted
Exercised
Canceled
Outstanding at December 31, 2020
Exercisable at December 31, 2020
0.6
0.1
(0.2)
—
0.5
0.3
125.26
182.71
93.55
—
148.39
126.55
6.5
4.9
$
$
27.5
20.5
The aggregate intrinsic value in the table above represents the total pre-tax intrinsic value (the difference between the
Company’s closing stock price on the last trading day of 2020 and the exercise price, multiplied by the number of in-the-money
options) that would have been received by the option holders had all option holders exercised their options on December 31,
2020.
Cash received by the Company from option exercises, the actual tax benefit realized for the tax deductions and the
aggregate intrinsic value of options exercised from option exercises under all share-based payment arrangements during the
years ended December 31, 2020, 2019, and 2018 were as follows:
Cash received by the Company
Tax benefits realized
Aggregate intrinsic value
2020
2019
2018
$
$
$
17.5 $
4.6 $
18.5 $
27.6 $
6.9 $
24.5 $
37.5
9.4
44.1
The following table shows the weighted average grant-date fair values of options issued during the respective year and the
weighted average assumptions that the Company used to develop the fair value estimates:
Fair value per option
Weighted average expected life (in years)
Risk free interest rate
Expected volatility
Expected dividend yield
2020
40.06
$
2019
33.70
$
6.0
1.5 %
20.3 %
N/A
6.0
2.1 %
20.4 %
N/A
The Black Scholes model incorporates assumptions to value stock-based awards. The risk-free interest rate for periods
within the contractual life of the option is based on a zero-coupon U.S. government instrument over the contractual term of the
equity instrument. Expected volatility of the Company’s stock is based on historical volatility of the Company’s stock. The
Company estimates expected option terms through an analysis of actual, historical post-vesting exercise, cancellation and
expiration behavior by employees and projected post-vesting activity of outstanding options. Groups of employees and non-
employee directors that have similar exercise behavior with regard to option exercise timing and forfeiture rates are considered
separately for valuation purposes. For 2020, 2019 and 2018, expense related to the Company’s stock option plan totaled $3.4,
$5.9 and $3.5, respectively, and is included in selling, general and administrative expenses.
F-33
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Restricted Stock, Restricted Stock Units and Performance Shares
The Company grants restricted stock, restricted stock units, and performance shares (non-vested shares) to officers and key
employees and grants restricted stock and restricted stock units to non-employee directors. Restricted stock and units typically
vest annually in equal one-third increments beginning on the first anniversary of the grant. A performance share grant in 2018
represents a three-year award opportunity for the period 2018-2020, and if earned, vests fully (to the extent earned) in the first
quarter of 2021. A performance share grant in 2019 represents a three-year award opportunity for the period of 2019-2021 and,
if earned, vests fully (to the extent earned) in the first quarter of 2022. A performance share grant in 2020 represents a three-
year award opportunity for the period of 2020-2022 and, if earned, vests fully (to the extent earned) in the first quarter of 2023.
Performance share awards are subject to certain earnings per share, revenue, and total shareholder return targets, the
achievement of which may increase or decrease the number of shares which the grantee earns and therefore receives upon
vesting. Unearned restricted stock and performance share compensation is amortized to expense, when probable, over the
applicable vesting periods. For 2020, 2019, and 2018, total restricted stock, restricted stock unit, and performance share
compensation expense was $98.1, $91.2 and $80.1, respectively, and is included in selling, general and administrative expenses.
The following table shows a summary of non-vested shares for the year ended December 31, 2020:
Non-vested at January 1, 2020
Granted
Vested
Canceled
Non-vested at December 31, 2019
Number of
Shares
Weighted-Average
Grant Date Fair Value
152.70
182.88
144.55
167.56
170.04
1.3 $
0.7
(0.6)
(0.1)
1.3 $
As of December 31, 2020, there was $115.5 of total unrecognized compensation cost related to non-vested stock options,
restricted stock, restricted stock unit and performance share-based compensation arrangements granted under the Company's
stock incentive plans. That cost is expected to be recognized over a weighted average period of 1.8 years and will be included in
selling, general and administrative expenses.
Employee Stock Purchase Plan
Under the 2016 Employee Stock Purchase Plan, the Company is authorized to issue 1.8 shares of common stock. The plan
permits substantially all U.S. employees to purchase a limited number of shares of Company stock at 85% of market value. The
Company issues shares to participating employees semi-annually in January and July of each year. Approximately 0.3, 0.2 and
0.2 shares were purchased by eligible employees in 2020, 2019 and 2018, respectively. For 2020, 2019 and 2018, expense
related to the Company’s employee stock purchase plan was $10.3, $9.9 and $8.0, respectively.
The Company uses the Black-Scholes model to calculate the fair value of the employee’s purchase right. The fair value of
the employee’s purchase right and the assumptions used in its calculation are as follows:
Fair value of the employee’s purchase right
Valuation assumptions
Risk free interest rate
Expected volatility
Expected dividend yield
2020
35.49
$
2019
31.84
$
2018
34.43
$
0.1 %
0.3
—
1.9 %
0.2
—
2.3 %
0.2
—
16. COMMITMENTS AND CONTINGENT LIABILITIES
The Company is involved from time to time in various claims and legal actions, including arbitrations, class actions, and
other litigation (including those described in more detail below), arising in the ordinary course of business. Some of these
actions involve claims that are substantial in amount. These matters include, but are not limited to, intellectual property
disputes; commercial and contract disputes; professional liability claims; employee-related matters; and inquiries, including
subpoenas and other civil investigative demands, from governmental agencies, Medicare or Medicaid payers and MCOs
reviewing billing practices or requesting comment on allegations of billing irregularities that are brought to their attention
through billing audits or third parties. The Company receives civil investigative demands or other inquiries from various
governmental bodies in the ordinary course of its business. Such inquiries can relate to the Company or other parties, including
physicians and other health care providers. The Company works cooperatively to respond to appropriate requests for
information.
F-34
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
The Company also is named from time to time in suits brought under the qui tam provisions of the False Claims Act and
comparable state laws. These suits typically allege that the Company has made false statements and/or certifications in
connection with claims for payment from U.S. federal or state healthcare programs. The suits may remain under seal (hence,
unknown to the Company) for some time while the government decides whether to intervene on behalf of the qui tam plaintiff.
Such claims are an inevitable part of doing business in the healthcare field today.
The Company believes that it is in compliance in all material respects with all statutes, regulations, and other requirements
applicable to its commercial laboratory operations and drug development support services. The healthcare diagnostics and drug
development industries are, however, subject to extensive regulation, and the courts have not interpreted many of the applicable
statutes and regulations. Therefore, the applicable statutes and regulations could be interpreted or applied by a prosecutorial,
regulatory, or judicial authority in a manner that would adversely affect the Company. Potential sanctions for violation of these
statutes and regulations include significant civil and criminal penalties, fines, the loss of various licenses, certificates and
authorizations, additional liabilities from third-party claims, and/or exclusion from participation in government programs.
Many of the current claims and legal actions against the Company are in preliminary stages, and many of these cases seek an
indeterminate amount of damages. The Company records an aggregate legal reserve, which is determined using calculations
based on historical loss rates and assessment of trends experienced in settlements and defense costs. In accordance with FASB
Accounting Standards Codification Topic 450 “Contingencies,” the Company establishes reserves for judicial, regulatory, and
arbitration matters outside the aggregate legal reserve if and when those matters present loss contingencies that are both
probable and estimable and would exceed the aggregate legal reserve. When loss contingencies are not both probable and
estimable, the Company does not establish separate reserves.
The Company is unable to estimate a range of reasonably probable loss for the proceedings described in more detail below
in which damages either have not been specified or, in the Company's judgment, are unsupported and/or exaggerated and (i) the
proceedings are in early stages; (ii) there is uncertainty as to the outcome of pending appeals or motions; (iii) there are
significant factual issues to be resolved; and/or (iv) there are novel legal issues to be presented. For these proceedings, however,
the Company does not believe, based on currently available information, that the outcomes will have a material adverse effect
on the Company's financial condition, though the outcomes could be material to the Company's operating results or cash flows
for any particular period, depending, in part, upon the operating results for such period.
As previously reported, the Company responded to an October 2007 subpoena from the U.S. Department of Health &
Human Services Office of Inspector General's regional office in New York. On August 17, 2011, the U.S. District Court for the
Southern District of New York unsealed a False Claims Act lawsuit, United States of America ex rel. NPT Associates v.
Laboratory Corporation of America Holdings, which alleges that the Company offered UnitedHealthcare kickbacks in the form
of discounts in return for Medicare business. The Plaintiff's Third Amended Complaint further alleges that the Company's
billing practices violated the False Claims Acts of 14 states and the District of Columbia. The lawsuit seeks actual and treble
damages and civil penalties for each alleged false claim, as well as recovery of costs, attorney's fees, and legal expenses.
Neither the U.S. government nor any state government has intervened in the lawsuit. The Company's Motion to Dismiss was
granted in October 2014 and Plaintiff was granted the right to replead. On January 11, 2016, Plaintiff filed a motion requesting
leave to file an amended complaint under seal and to vacate the briefing schedule for the Company's Motion to Dismiss, while
the government reviews the amended complaint. The Court granted the motion and vacated the briefing dates. Plaintiff then
filed the Amended Complaint under seal. The Company will vigorously defend the lawsuit.
In addition, the Company has received various other subpoenas since 2007 related to Medicaid billing. In October 2009, the
Company received a subpoena from the State of Michigan Department of Attorney General seeking documents related to its
billing to Michigan Medicaid. The Company cooperated with this request. In October 2013, the Company received a Civil
Investigative Demand from the State of Texas Office of the Attorney General requesting documents related to its billing to
Texas Medicaid. The Company cooperated with this request. On October 5, 2018, the Company received a second Civil
Investigative Demand from the State of Texas Office of the Attorney General requesting documents related to its billing to
Texas Medicaid. The Company cooperated with this request. On January 26, 2021, the Company was notified that a qui tam
Petition was pending under seal in the District Court, 250th Judicial District, Travis County, Texas, and that the State of Texas
has intervened. The petition remains under seal. If the petition is unsealed and served upon the Company, the Company will
vigorously defend the lawsuit.
On August 31, 2015, the Company was served with a putative class action lawsuit, Patty Davis v. Laboratory Corporation
of America, et al., filed in the Circuit Court of the Thirteenth Judicial Circuit for Hillsborough County, Florida. The complaint
alleges that the Company violated the Florida Consumer Collection Practices Act by billing patients who were collecting
benefits under the Workers' Compensation Statutes. The lawsuit seeks injunctive relief and actual and statutory damages, as
well as recovery of attorney's fees and legal expenses. In April 2017, the Circuit Court granted the Company’s Motion for
F-35
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Judgment on the Pleadings. The Plaintiff appealed the Circuit Court’s ruling to the Florida Second District Court of Appeal. On
October 16, 2019, the Court of Appeal reversed the Circuit Court’s dismissal, but certified a controlling issue of Florida law to
the Florida Supreme Court. On February 17, 2020, the Florida Supreme Court accepted jurisdiction of the lawsuit. The Court
held oral arguments on December 9, 2020. The Company will vigorously defend the lawsuit.
In December 2014, the Company received a Civil Investigative Demand issued pursuant to the U.S. False Claims Act from
the U.S. Attorney's Office for South Carolina, which requested information regarding alleged remuneration and services
provided by the Company to physicians who also received draw and processing/handling fees from competitor laboratories
Health Diagnostic Laboratory, Inc. (HDL) and Singulex, Inc. (Singulex). The Company cooperated with the request. On April
4, 2018, the U.S. District Court for the District of South Carolina, Beaufort Division, unsealed a False Claims Act lawsuit,
United States of America ex rel. Scarlett Lutz, et al. v. Laboratory Corporation of America Holdings, which alleges that the
Company's financial relationships with referring physicians violate federal and state anti-kickback statutes. The Plaintiffs'
Fourth Amended Complaint further alleges that the Company conspired with HDL and Singulex in violation of the Federal
False Claims Act and the California and Illinois insurance fraud prevention acts by facilitating HDL's and Singulex's offers of
illegal inducements to physicians and the referral of patients to HDL and Singulex for laboratory testing. The lawsuit seeks
actual and treble damages and civil penalties for each alleged false claim, as well as recovery of costs, attorney's fees, and legal
expenses. Neither the U.S. government nor any state government has intervened in the lawsuit. The Company filed a Motion to
Dismiss seeking the dismissal of the claims asserted under the California and Illinois insurance fraud prevention statutes, the
conspiracy claim, the reverse False Claims Act claim, and all claims based on the theory that the Company performed medically
unnecessary testing. On January 16, 2019, the Court entered an order granting in part and denying in part the Motion to
Dismiss. The Court dismissed the Plaintiffs' claims based on the theory that the Company performed medically unnecessary
testing, the claims asserted under the California and Illinois insurance fraud prevention statutes, and the reverse False Claims
Act claim. The Court denied the Motion to Dismiss as to the conspiracy claim. The Company will vigorously defend the
lawsuit.
Prior to the Company's acquisition of Sequenom, Inc. (Sequenom) between August 15, 2016 and August 24, 2016, six
putative class-action lawsuits were filed on behalf of purported Sequenom stockholders (captioned Malkoff v. Sequenom, Inc.,
et al., No. 16-cv-02054- JAH-BLM, Gupta v. Sequenom, Inc., et al., No. 16-cv-02084-JAH-KSC, Fruchter v. Sequenom, Inc.,
et al., No. 16-cv-02101- WQH-KSC, Asiatrade Development Ltd. v. Sequenom, Inc., et al., No. 16-cv-02113-AJB-JMA, Nunes
v. Sequenom, Inc., et al., No. 16-cv-02128-AJB-MDD, and Cusumano v. Sequenom, Inc., et al., No. 16-cv-02134-LAB-JMA)
in the U.S. District Court for the Southern District of California challenging the acquisition transaction. The complaints asserted
claims against Sequenom and members of its board of directors (the Individual Defendants). The Nunes action also named the
Company and Savoy Acquisition Corp. (Savoy), a wholly owned subsidiary of the Company, as defendants. The complaints
alleged that the defendants violated Sections 14(e), 14(d)(4) and 20 of the Securities Exchange Act of 1934 by failing to
disclose certain allegedly material information. In addition, the complaints in the Malkoff action, the Asiatrade action, and the
Cusumano action alleged that the Individual Defendants breached their fiduciary duties to Sequenom shareholders. The actions
sought, among other things, injunctive relief enjoining the merger. On August 30, 2016, the parties entered into a Memorandum
of Understanding (MOU) in each of the above-referenced actions. On September 6, 2016, the Court entered an order
consolidating for all pre-trial purposes the six individual actions described above under the caption In re Sequenom, Inc.
Shareholder Litig., Lead Case No. 16-cv-02054-JAH-BLM, and designating the complaint from the Malkoff action as the
operative complaint for the consolidated action. On November 11, 2016, two competing motions were filed by two separate
stockholders (James Reilly and Shikha Gupta) seeking appointment as lead plaintiff under the terms of the Private Securities
Litigation Reform Act of 1995. On June 7, 2017, the Court entered an order declaring Mr. Reilly as the lead plaintiff and
approving Mr. Reilly's selection of lead counsel. The parties agree that the MOU has been terminated. The Plaintiffs filed a
Consolidated Amended Class Action Complaint on July 24, 2017, and the Defendants filed a Motion to Dismiss, which remains
pending. On March 13, 2019, the Court stayed the action in its entirety pending the U.S. Supreme Court's anticipated decision
in Emulex Corp. v. Varjabedian. On April 23, 2019, however, the U.S. Supreme Court dismissed the writ of certiorari in
Emulex as improvidently granted. The Company will vigorously defend the lawsuit.
On March 10, 2017, the Company was served with a putative class action lawsuit, Victoria Bouffard, et al. v. Laboratory
Corporation of America Holdings, filed in the U.S. District Court for the Middle District of North Carolina. The complaint
alleges that the Company's patient list prices unlawfully exceed the rates negotiated for the same services with private and
public health insurers in violation of various state consumer protection laws. The lawsuit also alleges breach of implied contract
or quasi-contract, unjust enrichment, and fraud. The lawsuit seeks statutory, exemplary, and punitive damages, injunctive relief,
and recovery of attorney's fees and costs. In May 2017, the Company filed a Motion to Dismiss Plaintiffs' Complaint and Strike
Class Allegations; the Motion to Dismiss was granted in March 2018 without prejudice. On October 10, 2017, a second putative
class action lawsuit, Sheryl Anderson, et al. v. Laboratory Corporation of America Holdings, was filed in the U.S. District
F-36
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Court for the Middle District of North Carolina. The complaint contained similar allegations and sought similar relief to the
Bouffard complaint, and added additional counts regarding state consumer protection laws. On August 10, 2018, the Plaintiffs
filed an Amended Complaint, which consolidated the Bouffard and Anderson actions. On September 10, 2018, the Company
filed a Motion to Dismiss Plaintiffs' Amended Complaint and Strike Class Allegations. On August 16, 2019, the Court entered
an order granting in part and denying in part the Motion to Dismiss the Amended Complaint, and denying the Motion to Strike
the Class Allegations. The Company will vigorously defend the lawsuit.
On April 1, 2019, Covance Research Products was served with a Grand Jury Subpoena issued by the Department of Justice
(DOJ) in Miami, Florida requiring the production of documents related to the importation into the United States of live non-
human primate shipments originating from or transiting through China, Cambodia, and/or Vietnam from April 1, 2014 through
March 28, 2019. The Company is cooperating with the DOJ.
On May 14, 2019, Retrieval-Masters Creditors Bureau, Inc. d/b/a American Medical Collection Agency (AMCA), an
external collection agency, notified the Company about a security incident AMCA experienced that may have involved certain
personal information about some of the Company’s patients (the AMCA Incident). The Company referred patient balances to
AMCA only when direct collection efforts were unsuccessful. The Company’s systems were not impacted by the AMCA
Incident. Upon learning of the AMCA Incident, the Company promptly stopped sending new collection requests to AMCA and
stopped AMCA from continuing to work on any pending collection requests from the Company. AMCA informed the
Company that it appeared that an unauthorized user had access to AMCA’s system between August 1, 2018, and March 30,
2019, and that AMCA could not rule out the possibility that personal information on AMCA’s system was at risk during that
time period. Information on AMCA’s affected system from the Company may have included name, address, and balance
information for the patient and person responsible for payment, along with the patient’s phone number, date of birth, referring
physician, and date of service. The Company was later informed by AMCA that health insurance information may have been
included for some individuals, and because some insurance carriers utilize the Social Security Number as a subscriber
identification number, the Social Security Number for some individuals may also have been affected. No ordered tests,
laboratory test results, or diagnostic information from the Company were in the AMCA affected system. The Company notified
individuals for whom it had a valid mailing address. For the individuals whose Social Security Number was affected, the notice
included an offer to enroll in credit monitoring and identity protection services that will be provided free of charge for 24
months.
Twenty-three putative class action lawsuits were filed against the Company related to the AMCA Incident in various U.S.
District Courts. Numerous similar lawsuits have been filed against other health care providers who used AMCA. These lawsuits
have been consolidated into a multidistrict litigation in the District of New Jersey. On November 15, 2019, the Plaintiffs filed a
Consolidated Class Action Complaint in the U.S. District Court of New Jersey. On January 22, 2020, the Company filed
Motions to Dismiss all claims. The consolidated Complaint generally alleges that the Company did not adequately protect its
patients’ data and failed to timely notify those patients of the AMCA Incident. The Complaint asserts various causes of action,
including but not limited to negligence, breach of implied contract, unjust enrichment, and the violation of state data protection
statutes. The Complaint seeks damages on behalf of a class of all affected Company customers. The Company will vigorously
defend the multi-district litigation.
The Company was served with a shareholder derivative lawsuit, Raymond Eugenio, Derivatively on Behalf of Nominal
Defendant, Laboratory Corporation of America Holdings v. Lance Berberian, et al., filed in the Court of Chancery of the State
of Delaware on April 23, 2020. The complaint asserts derivative claims on the Company’s behalf against the Company’s board
of directors and certain executive officers. The complaint generally alleges that the defendants failed to ensure that the
Company utilized proper cybersecurity safeguards and failed to implement a sufficient response to data security incidents,
including the AMCA Incident. The complaint asserts derivative claims for breach of fiduciary duty and seeks relief including
damages, certain disclosures, and certain changes to the Company’s internal governance practices. On June 2, 2020, the
Company filed a Motion to Stay the lawsuit due to its overlap with the multi-district litigation referenced above. On July 2,
2020, the Company filed a Motion to Dismiss. On July 14, 2020, the Court entered an order staying the lawsuit pending the
resolution of the multi-district litigation. The lawsuit will be vigorously defended.
Certain governmental entities have requested information from the Company related to the AMCA Incident. The Company
received a request for information from the Office for Civil Rights (OCR) of the Department of Health and Human
Services. On April 28, 2020, OCR notified the Company of the closure of its inquiry. The Company has also received requests
from a multi-state group of state Attorneys General and is cooperating with these requests for information.
Three putative class action lawsuits related to California wage and hour laws have been served on the Company. On
September 21, 2018, the Company was served with a putative class action lawsuit, Alma Haro v. Laboratory Corporation of
F-37
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
America, et al., filed in the Superior Court of California, County of Los Angeles. On June 10, 2019, the Company was served
with a putative class action lawsuit, Ignacio v. Laboratory Corporation of America, filed in Superior Court of California,
County of Los Angeles. On July 1, 2019, the Company was served with a putative class action lawsuit, Jan v. Laboratory
Corporation of America, filed in the Superior Court of California, County of Sacramento. All three lawsuits were subsequently
removed to the U.S. District Court for the Central District of California, and then consolidated for all pre-trial proceedings. In
the lawsuits, the Plaintiffs allege that employees were not properly paid overtime compensation, minimum wages, meal and rest
break premiums, did not receive compliant wage statements, and were not properly paid wages upon termination of
employment. The Plaintiffs assert these actions violate various California Labor Code provisions and constitute an unfair
competition practice under California law. The lawsuits seek monetary damages, civil penalties, and recovery of attorney's fees
and costs. On July 22, 2020, the Court issued an order granting preliminary approval of a settlement resolving all three lawsuits.
On November 18, 2020, the Court granted final approval of the settlement and settlement proceeds have been distributed.
On January 31, 2020, the Company was served with a putative class action lawsuit, Luke Davis and Julian Vargas, et al. v.
Laboratory Corporation of America Holdings, filed in the U.S. District Court for the Central District of California. The lawsuit
alleges that visually impaired patients are unable to use the Company's touchscreen kiosks at Company patient service centers
in violation of the Americans with Disabilities Act and similar California statutes. The lawsuit seeks statutory damages,
injunctive relief, and attorney's fees and costs. On March 20, 2020, the Company filed a Motion to Dismiss Plaintiffs'
Complaint and to Strike Class Allegations. In August 2020, the Plaintiffs filed an Amended Complaint. The Company will
vigorously defend the lawsuit.
On May 14, 2020, the Company was served with a putative class action lawsuit, Jose Bermejo v. Laboratory Corporation of
America (Bermejo I) filed in the Superior Court of California, County of Los Angeles Central District, alleging that certain non-
exempt California-based employees were not properly compensated for driving time or properly paid wages upon termination
of employment. The Plaintiff asserts these actions violate various California Labor Code provisions and Section 17200 of the
Business and Professional Code. The lawsuit seeks monetary damages, civil penalties, and recovery of attorney’s fees and
costs. On June 15, 2020, the lawsuit was removed to the U.S. District Court for the Central District of California. On June 16,
2020, the Company was served with a Private Attorney General Act lawsuit by the same plaintiff in Jose Bermejo v. Laboratory
Corporation of America (Bermejo II), filed in the Superior Court of California, County of Los Angeles Central District, alleging
that certain Company practices violated California Labor Code penalty provisions related to unpaid and minimum wages,
unpaid overtime, unpaid mean and rest break premiums, untimely payment of wages following separation of employment,
failure to maintain accurate pay records, and non-reimbursement of business expenses. The second lawsuit seeks to recover
civil penalties and recovery of attorney's fees and costs. On October 28, 2020, the court issued an order staying proceedings in
Bermejo II pending resolution of Bermejo I. The second lawsuit seeks to recover civil penalties and recovery of attorney's fees
and costs. The Company will vigorously defend both lawsuits.
On August 14, 2020, the Company was served with a Subpoena Duces Tecum issued by the State of Colorado Office of the
Attorney General requiring the production of documents related to urine drug testing in all states. The Company is cooperating
with this request.
On October 2, 2020, the Company was served with a putative class action lawsuit, Peterson v. Laboratory Corporation of
America Holdings, filed in the U.S. District Court for the Northern District of New York, alleging claims for a failure to
properly pay service representatives compensation for all hours worked and overtime under the Fair Labor Standards Act, as
well as notice and recordkeeping claims under the New York Labor Code. The lawsuit seeks monetary damages, liquidated
damages, equitable and injunctive relief, and recovery of attorney's fees and costs. The Company will vigorously defend the
lawsuit.
On October 5, 2020, the Company was served with a putative class action lawsuit, Williams v. Labcorp Employer Services,
Inc. et al., filed in the Superior Court of California, County of Los Angeles, alleging that certain non-exempt California-based
employees were not properly compensated for work and overtime hours, not properly paid meal and rest break premiums, not
reimbursed for certain business-related expenses, not properly paid for driving or wait times, and received inaccurate wage
statements. The Plaintiff also asserts claims for unfair competition under Section 17200 of the Business and Professional Code.
The lawsuit seeks monetary damages, liquidated damages, civil penalties, and recovery of attorney's fees and costs. The
Company will vigorously defend the lawsuit.
Under the Company's present insurance programs, coverage is obtained for catastrophic exposure as well as those risks
required to be insured by law or contract. The Company is responsible for the uninsured portion of losses related primarily to
general, professional and vehicle liability, certain medical costs and workers' compensation. The self-insured retentions are on a
F-38
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
per-occurrence basis without any aggregate annual limit. Provisions for losses expected under these programs are recorded
based upon the Company's estimates of the aggregated liability of claims incurred.
17. PENSION AND POSTRETIREMENT PLANS
Defined Contribution Retirement Plans
The Company has various defined contribution retirement plans (401K Plans). Under these 401K Plans, employees can
contribute a portion of their salary to the plan and the Company makes minimum non-elective contributions, discretionary
contributions, and matching contributions, depending on the terms of the specific plan. On January 1, 2021, all of the 401K
Plans were modified to provide for 100% match of employee contributions up to 5% of their salary. Total expense, for the years
ended December 31, 2020, 2019, and 2018, was $141.8, $139.5 and $129.9, respectively.
Defined Benefit Pension Plans
The Company sponsors both funded and unfunded defined benefit pension plans which provide benefits based on various
criteria such as years of service and salary. The Company maintained two plans in the United States, three plans in the United
Kingdom and one in Germany.
The two plans in the United States (U.S. Plans) were closed to new entrants and the accrual of service credits at the end of
2009. The U.K. pension plans were closed to new entrants and the accrual of service credits for one plan as of December 31,
2002, and the accrual of service credits for the other two plans as of December 31, 2019. The German plan is closed to new
entrants but participants continue to accrue service credits. The U.K. and German plans are aggregated for disclosure as the
Non-U.S. Plans.
Net Periodic Benefit Costs
The components of the net periodic benefit costs for the defined benefit pension plans are as follows:
U. S. Plans
Non-U.S. Plans
Year ended December 31,
2020
2019
2018
2020
2019
2018
Service cost for benefits earned
Interest cost on benefit obligation
Expected return on plan assets
Net amortization and deferral
Expected participant contributions
Settlements
Defined-benefit plan costs
$
$
5.1 $
11.1
(14.9)
9.7
—
—
11.0 $
4.1 $
13.9
(15.1)
10.9
—
—
13.8 $
5.2
13.0
(16.5)
11.7
—
7.5
20.9
2.1
10.9
(16.6)
0.4
(0.1)
—
(3.3)
5.7
10.9
(15.0)
—
(1.2)
—
0.4
6.0
8.0
(12.6)
—
(1.3)
—
0.1
Net periodic benefit costs are recorded as a component of Operating income. For the year ended December 31, 2018, the
Company recognized a partial plan settlement charge of $7.5 as a component of Other, net.
The amounts recognized in accumulated other comprehensive earnings are as follows:
Net actuarial loss in accumulated other comprehensive earnings $
108.8 $
111.2 $
99.7 $
31.5
U. S. Plans
Non-U.S. Plans
Year ended December 31,
2020
2019
2020
2019
F-39
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Change in Projected Benefit Obligation
The change in the projected benefit obligation as of December 31, 2020, and December 31, 2019, is as follows:
Balance at beginning of the year
Balance of acquired subsidiary at acquisition date
Service cost
Interest cost
Actuarial (gain) loss
Benefits and administrative expenses paid
Plan curtailment
Foreign currency exchange rate changes
Balance at end of the year
U.S. Plans
Non-U.S. Plans
Year Ended December 31,
2020
2019
2020
2019
$
$
355.5 $
—
5.1
11.1
24.7
(26.6)
—
—
369.8 $
334.6 $
—
4.1
13.9
33.3
(30.4)
—
—
355.5 $
590.7 $
—
2.1
10.9
80.5
(20.0)
—
25.9
690.1 $
294.1
215.4
5.7
10.9
72.3
(11.6)
(16.1)
20.0
590.7
The accumulated benefit obligation as of December 31, 2020 and 2019 was $369.8 and $355.5, respectively for the U.S.
Plans and $683.3 and $585.8, respectively for the Non-U.S. Plans. The increase in the projected benefit obligation for the U.S.
Plans from December 31, 2019 to December 31, 2020 is primarily due to an increase of $30.8 as a result of discount rate and
mortality rate changes partially offset by the net of normal plan progression and experience gains of $16.5. The increase in the
projected benefit obligation for the Non-U.S. Plans from December 31, 2019 to December 31, 2020 is primarily due to an
increase of $83.2 as a result of discount rate changes and an increase of $25.9 due to foreign currency exchange rate changes,
partially offset by the net of normal plan progress and experience gains of $9.8.
Change in Fair Value of Plan Assets
The change in plan assets as of December 31, 2020, and December 31, 2019, is as follows:
Balances at beginning of the year
Plan assets of acquired subsidiary at acquisition date
Company contributions
Participant contributions
Actual return on plan assets
Benefits and administrative expenses paid
Foreign currency exchange rate changes
Fair value of plan assets at end of year
U.S. Plans
Non-U.S. Plans
Year Ended December 31,
2020
2019
2020
2019
$
$
262.1 $
—
33.1
—
32.3
(26.6)
—
300.9 $
246.9 $
—
2.2
—
43.4
(30.4)
—
262.1 $
491.7 $
—
13.5
0.1
32.8
(19.6)
17.1
535.6 $
254.6
168.3
11.4
1.3
48.8
(11.3)
18.6
491.7
Change in Funded Status and Reconciliation of Amounts Recorded in the Balance Sheet
The change in the funded status of the plan and a reconciliation of such funded status to the amounts reported in the
consolidated balance sheet as of December 31, 2020, and December 31, 2019, is as follows:
Funded status
Recorded as:
Accrued expenses and other
Other liabilities
U.S. Plans
Non-U.S. Plans
Year Ended December 31,
2020
68.9 $
2019
93.4 $
2020
154.5 $
2019
99.1
2.3 $
66.6
2.2 $
91.2
0.6 $
153.9
0.5
98.6
$
$
F-40
Index
Assumptions
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Weighted average assumptions used to determine net periodic benefit costs are as follows:
Discount rate
Salary increases
Expected long term rate of return
Cash balance interest credit rate
U. S. Plans
Non-U.S. Plans
Year ended December 31,
2020
3.3 %
N/A
6.0 %
4.0 %
2019
4.3 %
N/A
6.5 %
4.0 %
2018
3.6 %
N/A
6.5 %
4.0 %
2020
1.7 %
3.1 %
3.5 %
N/A
2019
2.2 %
2.7 %
4.2 %
N/A
2018
2.1 %
2.7 %
4.5 %
N/A
Weighted average assumptions used to determine net periodic benefit obligations are as follows:
Discount rate
Salary increases
U. S. Plans
Non-U.S. Plans
Year ended December 31,
2020
2.3 %
N/A
2019
3.3 %
N/A
2020
1.2 %
2.0 %
2019
1.9 %
3.3 %
The discount rate is determined using the weighted-average yields on high-quality fixed income securities that have
maturities consistent with the timing of benefit payments. Lower discount rates increase the size of the benefit obligation and
generally increase pension expense in the following year; higher discount rates reduce the size of the benefit obligation and
generally reduce subsequent-year pension expense.
The expected return on plan assets is the estimated long-term rate of return that will be earned on the investments used to
fund the pension obligations. To determine this rate, the Company considers the composition of plan investments, historical
returns earned, and expectations about the future.
The salary increase assumptions are used to estimate the annual rate at which pay of plan participants will grow. If the rate
of growth assumed increases, the size of the pension obligations will increase, as will the amount recorded in Accumulated
other comprehensive income (loss) in our consolidated Statement of Financial Position and amortized into earnings in
subsequent periods.
The Company evaluates other assumptions periodically, such as retirement age, mortality and turnover, and updates them as
necessary to reflect our actual experience and expectations for the future. Differences between actual results and assumptions
utilized are recorded in Accumulated other comprehensive income each period. These differences are amortized into earnings
over the remaining average future service of active participating employees or the expected life of inactive participants, as
applicable.
F-41
Index
Plan Assets
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
The fair values of the assets at December 31, 2020, and 2019, by asset category are as follows:
Asset Category
U.S Plans
Cash and cash equivalents
U.S. equity index funds
International equity index funds
Real estate
General bond index funds
Total fair value
Non U.S. Plans
Cash and cash equivalents
Annuities
Pooled investment funds
Total fair value
Asset Category
U.S Plans
Cash and cash equivalents
U.S. equity index funds
International equity index funds
Real estate index fund
General bond index funds
Total fair value
Non U.S. Plans
Cash and cash equivalents
Annuities
Pooled investment funds
Total fair value
Level of
Valuation Input
Fair Value
Investments valued using
NAV per share
Total
Level 1
$
Level 1
Level 3
$
$
$
13.0 $
—
—
—
—
13.0 $
6.8 $
58.7
—
65.5 $
— $
105.5
45.7
15.0
121.7
287.9 $
— $
—
470.1
470.1 $
Level of
Valuation Input
Fair Value
Investments valued using
NAV per share
Total
Level 1
$
Level 1
Level 3
$
$
$
4.3 $
—
—
—
—
4.3 $
2.6 $
30.6
—
33.2 $
— $
93.4
40.6
12.7
111.1
257.8 $
— $
—
458.5
458.5 $
13.0
105.5
45.7
15.0
121.7
300.9
6.8
58.7
470.1
535.6
4.3
93.4
40.6
12.7
111.1
262.1
2.6
30.6
458.5
491.7
The fair market value of index funds and pooled investment funds are valued using the net asset value (NAV) unit price
provided by the fund administrator. The NAV is based on the value of the underlying assets owned by the fund. The fair value
of annuity investments are based on discounted cash flow techniques using unobservable valuation inputs such as discount rates
and actuarial mortality tables.
Fair Value Measurement of Level 3 Pension Assets
Balance at January 1, 2019
Actual return on plan assets
Balance at December 31, 2019
Actual return on plan assets
Balance at December 31, 2020
Annuities
27.3
3.3
30.6
28.1
58.7
$
$
Investment Policies
Plan fiduciaries of various plans set investment policies and strategies, based on consultation with professional advisors,
and oversee investment allocation, which includes selecting investment managers and setting long-term strategic targets. The
primary strategic investment objectives are balancing investment risk and return and monitoring the plan’s liquidity position in
order to meet the near-term benefit payment and other cash needs. Target allocation percentages are established at an asset class
level by plan fiduciaries. Target allocation ranges are guidelines, not limitations, and occasionally plan fiduciaries will approve
allocations above or below a target range.
F-42
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
The weighted average asset allocation of the plan assets as of December 31, 2020, by asset category is as follows:
Equity securities
Debt securities
Annuities
Real estate
Other
The weighted average target asset allocation of the plan assets is as follows:
Equity securities
Debt securities
Annuities
Real estate
Other
Pension Funding and Cash Flows
December 31, 2020
U.S. Plans
Non-U.S. Plans
50.3 %
40.4 %
— %
5.0 %
4.3 %
47.2 %
34.6 %
11.3 %
4.0 %
1.0 %
U.S Plans
Non U.S Plans
33.0% to
35.0% to
— % to
2.0 % to
— % to
62.0 % 45.0% to
52.0 % 29.0% to
— % 6.0% to
8.0 % 2.0% to
4.0 % —% to
55.0%
39.0%
13.0%
12.0%
5.0%
The Company expects to make approximately $16.5 in required contributions to its defined benefit pension plans during
2021. The Company targets funding the minimum required contributions but may make additional contributions into the
pension plans in 2021, depending upon factors such as how the funded status of those plans change or to reduce the
administrative costs of the plan.
The estimated benefit payments, which were used in the calculation of projected benefit obligations, are expected to be paid
as follows:
2021
2022
2023
2024
2025
Years 2026 to 2035
$
U. S. Plans
Non-U. S. Plans
15.4
16.4
17.3
18.7
18.4
102.8
26.8 $
27.0
26.3
25.7
25.4
116.0
Post-employment Retiree Health and Welfare Plan
The Company sponsors a post-employment retiree health and welfare plan for the benefit of eligible employees at certain
U.S. subsidiaries who retire after satisfying service and age requirements. This plan is funded on a pay-as-you-go basis and the
cost of providing these benefits is shared with the retirees.
Post-retirement Medical Plan
The Company assumed obligations under a subsidiary's post-retirement medical plan. Coverage under this plan is restricted
to a limited number of existing employees of the subsidiary. This plan is unfunded and the Company’s policy is to fund benefits
as claims are incurred. The effect on operations of the post-retirement medical plan is shown in the following table:
Service cost for benefits earned
Interest cost on benefit obligation
Net amortization and deferral
Post-retirement medical plan costs
Year ended December 31,
2020
2019
2018
$
$
— $
0.2
0.4
0.6 $
— $
0.3
0.4
0.7 $
—
0.3
(1.3)
(1.0)
Amounts included in accumulated other comprehensive earnings consist of unamortized net loss of $1.6 and $2.0.
F-43
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
A summary of the changes in the accumulated post-retirement benefit obligation follows:
Balance at January 1
Interest cost on benefit obligation
Actuarial loss
Benefits paid
Balance at December 31
Recorded as:
Accrued expenses and other
Other liabilities
2020
2019
$
$
$
$
6.5 $
0.2
—
(0.5)
6.2 $
0.8 $
5.4
6.2 $
6.9
0.3
—
(0.7)
6.5
0.8
5.7
6.5
The weighted-average discount rates used in the calculation of the accumulated post-retirement benefit obligation were 2.3%
and 3.2% as of December 31, 2020, and 2019, respectively. The healthcare cost trend rate was removed due to the expectation
of future funding to be at the same level as the previous year's funding.
The following assumed benefit payments under the Company's post-retirement benefit plan, which reflect expected future
service, as appropriate, and which were used in the calculation of projected benefit obligations, are expected to be paid as
follows:
2021
2022
2023
2024
2025
Years 2026 and thereafter
0.8
0.7
0.7
0.6
0.6
1.6
$
Deferred Compensation Plan
The Company has Deferred Compensation Plans (DCP) under which certain of its executives may elect to defer up to
100.0% of their annual cash incentive pay and/or up to 50.0% of their annual base salary and/or eligible commissions subject to
annual limits established by the U.S. government. The DCP provides executives a tax efficient strategy for retirement savings
and capital accumulation without significant cost to the Company. The Company makes no contributions to the DCP. Amounts
deferred by a participant are credited to a bookkeeping account maintained on behalf of each participant, which is used for
measurement and determination of amounts to be paid to a participant, or his or her designated beneficiary, pursuant to the
terms of the DCP. The amounts accrued under these plans were $89.2 and $76.7 at December 31, 2020, and 2019, respectively.
Deferred amounts are the Company's general unsecured obligations and are subject to claims by the Company's creditors. The
Company's general assets may be used to fund obligations and pay DCP benefits.
18. FAIR VALUE MEASUREMENTS
The Company’s population of financial assets and liabilities subject to fair value measurements as of December 31, 2020,
and 2019 were as follows:
Balance Sheet
Classification
Fair Value as of
December 31, 2020
Fair Value Measurements as of
December 31, 2020
Using Fair Value Hierarchy
Level 1
Level 2
Level 3
Noncontrolling interest put
Cross currency swaps
Cash surrender value of life insurance policies Other assets, net
Other liabilities
Deferred compensation liability
Other liabilities
Contingent consideration
Noncontrolling interest $
Other liabilities, net
F-44
16.2 $ — $ 16.2 $
40.4
90.6
89.2
13.9
—
—
—
—
40.4
90.6
89.2
—
—
—
—
—
13.9
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Balance Sheet
Classification
Fair Value as of
December 31, 2019
Fair Value Measurements as of
December 31, 2019
Using Fair Value Hierarchy
Level 1
Level 2
Level 3
Noncontrolling interest $
Noncontrolling interest put
Other liabilities
Interest rate swap
Cross currency swaps liability
Other liabilities
Cash surrender value of life insurance policies Other assets, net
Other liabilities
Deferred compensation liability
Other current assets
Investment in equity securities
Other liabilities
Contingent consideration
Fair Value Measurement of Level 3 Liabilities
Balance at January 1, 2019
Addition
Cash payments and adjustments
Balance at December 31, 2019
Addition
Cash payments and adjustments
Balance at December 31, 2020
15.8 $ — $ 15.8 $
1.5
3.2
80.2
76.7
9.1
9.9
—
—
—
—
9.1
—
1.5
3.2
80.2
76.7
—
—
—
—
—
—
—
—
9.9
Contingent Consideration
18.6
$
3.3
(12.0)
9.9
10.8
(6.8)
13.9
$
The Company has a noncontrolling interest put related to its Ontario subsidiary that has been classified as mezzanine equity
in the Company’s condensed consolidated balance sheets. The noncontrolling interest put is valued at its contractually
determined value, which approximates fair value. During the year ended December 31, 2020, the carrying value of the
noncontrolling interest put increased by $0.4 for foreign currency translation.
The Company offers certain employees the opportunity to participate in a DCP. A participant's deferrals are allocated by the
participant to one or more of 16 measurement funds, which are indexed to externally managed funds. From time to time, to
offset the cost of the growth in the participant's investment accounts, the Company purchases life insurance policies, with the
Company named as beneficiary of the policies. Changes in the cash surrender value of the life insurance policies are based upon
earnings and changes in the value of the underlying investments, which are typically invested in a similar manner to the
participants' allocations. Changes in the fair value of the DCP obligation are derived using quoted prices in active markets based
on the market price per unit multiplied by the number of units. The cash surrender value and the DCP obligations are classified
within Level 2 because their inputs are derived principally from observable market data by correlation to the hypothetical
investments.
Contingent accrued earn-out business acquisition consideration liabilities for which fair values are measured as Level 3
instruments. These contingent consideration liabilities were recorded at fair value on the acquisition date and are remeasured
quarterly based on the then assessed fair value and adjusted if necessary. The increases or decreases in the fair value of
contingent consideration payable can result from changes in anticipated revenue levels and changes in assumed discount
periods and rates. As the fair value measure is based on significant inputs that are not observable in the market, they are
categorized as Level 3.
The carrying amounts of cash and cash equivalents, accounts receivable, income taxes receivable, and accounts payable are
considered to be representative of their respective fair values due to their short-term nature. The fair market value of the Senior
Notes, based on market pricing, was approximately $6,121.8 and $6,140.6 as of December 31, 2020, and 2019, respectively.
The Company's note and debt instruments are considered Level 2 instruments, as the fair market values of these instruments are
determined using other observable inputs.
19. DERIVATIVE INSTRUMENTS AND HEDGING ACTIVITIES
The Company addresses its exposure to market risks, principally the market risk associated with changes in interest rates
and currency exchange rates, through a controlled program of risk management that includes, from time to time, the use of
derivative financial instruments. Although the Company’s zero-coupon subordinated notes contained features that were
considered to be embedded derivative instruments, the Company does not hold or issue derivative financial instruments for
trading purposes. The Company does not believe that its exposure to market risk is material to the Company’s financial position
or results of operations.
F-45
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
Interest Rate Swap
During the third quarter of 2013, the Company entered into two fixed-to-variable interest rate swap agreements for the
4.625% Senior Notes due 2020 with an aggregate notional amount of $600.0 and variable interest rates based on one-month
LIBOR plus 2.298% to hedge against changes in the fair value of a portion of the Company's long-term debt. The Company
exited one of these swap arrangements in December 2019 in connection with the redemption of $187.9 of the 4.625% Senior
Notes due 2020. The Company exited the remaining fixed-to-variable interest rate swap agreement in August 2020, in
connection with the redemption of the remaining $412.2 of its 4.625% Senior Notes due November 15, 2020, and recorded a
gain of $1.6 on the extinguishment. The gain was included in Other, net on the Consolidated Statement of Operations. These
derivative financial instruments were accounted for as fair value hedges which increased or decreased the value of the Senior
Notes with the offset being recorded as a component of other long-term assets or liabilities, as applicable. As the specific terms
and notional amounts of the derivative financial instruments match those of the fixed-rate debt being hedged, the derivative
instruments were assumed to be perfectly effective hedges and accordingly, there is no impact to the Company's consolidated
statements of operations. Cash flows from the interest rate swaps are including in operating activities.
Carrying amount of hedged liabilities
as of December 31,
Cumulative Amount of Fair Value
Hedging Adjustment Included in the
Carrying Amount of the Hedged
Liabilities as of December 31,
Balance Sheet Line Item in which Hedged Items are Included
Long-term debt, less current portion
— $
301.5
— $
1.5
2020
2019
2020
2019
Foreign Currency Forward Contracts
The Company periodically enters into foreign currency forward contracts, which are recognized as assets or liabilities at
their fair value. These contracts do not qualify for hedge accounting and the changes in fair value are recorded directly to
earnings. The contracts are short-term in nature and the fair value of these contracts is based on market prices for comparable
contracts. The fair value of these contracts is not significant as of December 31, 2020 and 2019.
Cross Currency Swaps
During the fourth quarter of 2018, the Company entered into six new USD to Swiss Franc cross-currency swap agreements
with an aggregate notional value of $600.0 and which are accounted for as a hedge against the impact of foreign exchange
movements on its net investment in a Swiss Franc functional currency subsidiary. Of the notional value, $300.0 matures in 2022
and $300.0 matures in 2025. These cross currency swaps maturing in 2022 and 2025 with an aggregate fair value of $26.0 and
$14.4 as of December 31, 2020, respectively, are included in other long-term liabilities. These cross currency swaps maturing in
2022 and 2025 with an aggregate fair value of $0.2 and $3.0 as of December 31, 2019, respectively, are included in other long-
term assets. Changes in the fair value of the cross-currency swaps are recorded as a component of the foreign currency
translation adjustment in accumulated other comprehensive income in the Consolidated Balance Sheet until the hedged item is
recognized in earnings. The cumulative amount of the fair value hedging adjustment included in the current value of the cross
currency swaps is $(40.4) for the year ended December 31, 2020, and was recognized as currency translation within the
Consolidated Statement of Comprehensive Earnings. There were no amounts reclassified from the Consolidated Statement of
Comprehensive Earnings to the Consolidated Statement of Operations during the year ended December 31, 2020.
The table below presents the fair value of derivatives on a gross basis and the balance sheet classification of those
instruments:
December 31, 2020
Fair Value of Derivative
U.S.
Dollar
Notional Asset
December 31, 2019
Fair Value of Derivative
U.S.
Dollar
Notional
Liability
Liability
Asset
—
—
—
40.4
—
600.0
1.5
3.2
—
—
300.0
600.0
Balance Sheet Caption
Derivatives Designated as Hedging Instruments
Interest rate swap
Cross currency swaps Other assets, net/Other liabilities
Prepaid expenses and other/Other liabilities
F-46
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
The table below provides information regarding the location and amount of pretax (gains) losses of derivatives designated in
fair value hedging relationships:
Interest rate swap contracts
Cross currency swaps
Amount of pre-tax gain/(loss) included in
other comprehensive income
Year Ended December 31,
Amounts reclassified to the
Statement of Operations
Year Ended December 31,
2020
2019
2018
2020
2019
2018
$
$
0.8 $
(43.6) $
6.7 $
6.0 $
(7.2) $
21.6 $
1.6 $
— $
1.6 $
— $
—
—
The Company recognized a gain of $1.6 and $1.6 on the extinguishment of its interest rate swap agreement in the years ended
December 31, 2020 and December 31, 2019, respectively, in connection with the redemption of the 4.625% Senior Notes due
2020. No gains or losses from derivative instruments classified as hedging instruments have been recognized into income for
the year ended December 31, 2018.
20. SUPPLEMENTAL CASH FLOW INFORMATION
Supplemental schedule of cash flow information:
Cash paid during period for:
Interest
Income taxes, net of refunds
Disclosure of non-cash financing and investing activities:
Conversion of zero-coupon convertible debt
Assets acquired under finance leases
Change in accrued property, plant and equipment
Floating rate secured note receivable due 2022 from the sale of CRP
21. BUSINESS SEGMENT INFORMATION
Years Ended December 31,
2020
2019
2018
$
216.6 $
500.0
248.9 $
216.8
296.2
349.7
—
—
(1.2)
—
8.4
48.7
2.7
110.0
0.3
0.6
22.1
—
The following table is a summary of segment information for the years ended December 31, 2020, 2019, and 2018. The
“management approach” has been used to present the following segment information. This approach is based upon the way the
management of the Company organizes segments within an enterprise for making operating decisions and assessing
performance. Financial information is reported on the basis that it is used internally by the chief operating decision maker
(CODM) for evaluating segment performance and deciding how to allocate resources to segments. The Company’s chief
executive officer has been identified as the CODM.
Segment asset information is not presented because it is not used by the CODM at the segment level. Operating earnings
(loss) of each segment represents revenues less directly identifiable expenses to arrive at operating income for the segment.
General management and administrative corporate expenses are included in general corporate expenses below.
F-47
Index
LABORATORY CORPORATION OF AMERICA HOLDINGS AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(Dollars and shares in millions, except per share data)
2020
2019
2018
Revenues:
Dx
DD
Intercompany eliminations and other
Total revenues
Operating Earnings:
Dx
DD
General corporate expenses
Total operating income
Non-operating expenses, net
Earnings before income taxes
Provision for income taxes
Net earnings
Less: Net income attributable to noncontrolling interests
Net income attributable to Laboratory Corporation of America Holdings
Depreciation and Amortization
Dx
DD
General corporate
Total depreciation and amortization
Geographic distribution of revenues
North America
Europe
Other
Total revenues
$
9,253.4 $
4,877.7
(152.6)
7,030.8
4,313.1
(10.5)
$ 13,978.5 $ 11,554.8 $ 11,333.4
7,000.1 $
4,578.1
(23.4)
$
$
$
$
2,634.9 $
37.3
(226.8)
2,445.4
(226.3)
2,219.1
662.1
1,557.0
(0.9)
1,556.1 $
1,086.0 $
411.5
(167.3)
1,330.2
(225.3)
1,104.9
280.0
824.9
(1.1)
823.8 $
1,166.7
303.6
(144.6)
1,325.7
(57.4)
1,268.3
384.4
883.9
(0.2)
883.7
2020
2019
2018
327.5 $
295.2
2
624.7 $
301.0 $
261.1
2.6
564.7 $
293.3
247.3
2.6
543.2
Dx
DD
Intercompany
Eliminations
and Other
Total
$
$
9,253.4 $
—
—
9,253.4 $
2,424.5 $
1,512.2
941.0
4,877.7 $
(152.6) $
—
—
(152.6) $
11,525.3
1,512.2
941.0
13,978.5
Geographic distribution of property, plant and equipment, net
North America
Europe
Other
Total property, plant and equipment, net
Dx
DD
Total
$
$
1,515.3 $
—
—
1,515.3 $
665.3 $
425.5
123.5
1,214.3 $
2,180.6
425.5
123.5
2,729.6
F-48
DESCRIPTION OF THE REGISTRANT’S SECURITIES
REGISTERED PURSUANT TO SECTION 12 OF THE
SECURITIES EXCHANGE ACT OF 1934
As of the date of the Annual Report on Form 10-K of which this exhibit forms a part, the only class of
securities of Laboratory Corporation of America Holdings (“we” and “our”) registered under Section 12 of the
Securities Exchange Act of 1934, as amended is our common stock, $0.10 par value per share.
DESCRIPTION OF COMMON STOCK
The following description of our common stock summarizes certain material terms and provisions of our
certificate of incorporation, by-laws, and the Delaware General Corporation Law (“DGCL”). For the complete terms
of our common stock, please refer to our certificate of incorporation and by-laws, which are incorporated by
reference as exhibits to the Annual Report on Form 10-K of which this exhibit is a part, and to the applicable
provisions of the DGCL.
Authorized Common Stock
We have authority to issue 265 million shares of Common Stock, par value $0.10 per share.
Rights of Common Stock
Voting Rights; Liquidation; Dividends. Holders of our common stock are entitled:
•
•
•
to one vote per share upon any matter, including, without limitation, the election of directors, on which
stockholders are entitled to vote;
upon our liquidation, dissolution or winding up, whether voluntary or involuntary, to participate in the
distribution of any assets remaining after the payment of all debts and liabilities, subject to any preferential
rights of holders of any outstanding shares of preferred stock; and
to receive dividends, which may be cumulative or non-cumulative, as may be lawfully declared from time
to time by our board of directors.
Other Rights and Restrictions. The holders of our common stock do not have any preemptive or
subscription rights to purchase additional securities issued by us, nor any rights to convert their common stock into
other of our securities or to have their shares of common stock redeemed by us. Our common stock is not subject to
redemption by us. Our certificate of incorporation and by-laws do not restrict the ability of a holder of common
stock to transfer his or her shares of common stock. Our by-laws provide that holders of our common stock may act
by written consent on any matters that could otherwise be brought at annual or special meetings.
Preferred Stock. Our board of directors has the authority, without further action by our stockholders, to
issue up to 30 million shares of preferred stock, par value $0.10 per share, in one or more classes or series and to fix
the number of shares, designations, relative rights (including voting, conversion, redemption, and dividend rights),
terms of redemption, preferences, and limitations of such series to the full extent now or hereafter permitted by the
DGCL.
1
Anti-Takeover Effects of Our Certificate of Incorporation and By-Law Provisions
Undesignated Preferred Stock. Because the board of directors has the power to establish the preferences and
rights of the shares of any additional series of preferred stock, it may afford holders of any preferred stock
preferences, powers and rights, including voting and dividend rights, senior to the rights of holders of the common
stock, which could adversely affect the holders of the common stock and could discourage a takeover of us even if a
change of control of our company would be beneficial to the interests of our stockholders.
Special Stockholder Meetings. Our by-laws provide that a special meeting of stockholders may be called only
by a resolution adopted by a majority of our board of directors or by stockholders owning at least 10% of our
outstanding common stock, subject to the requirements and procedures as set forth in our by-laws.
Stockholder Advance Notice Procedure. Our by-laws establish an advance notice procedure for stockholders
to make nominations of candidates for election as directors or to bring other business before an annual meeting of
our stockholders.
Section 203 of the Delaware General Corporation Law. We are subject to Section 203 of the DGCL
(“Section 203”), which, with specified exceptions, prohibits a Delaware corporation from engaging in any “business
combination” with any “interested stockholder” for a period of three years following the time that the stockholder
became an interested stockholder unless:
•
•
•
prior to that time, the board of directors of the corporation approved either the business combination or the
transaction which resulted in the stockholder becoming an interested stockholder;
upon consummation of the transaction which resulted in the stockholder becoming an interested
stockholder, the interested stockholder owned at least 85% of the voting stock of the corporation
outstanding at the time the transaction commenced, excluding for purposes of determining the number of
shares outstanding those shares owned by persons who are directors and also officers and by employee
stock plans in which employee participants do not have the right to determine confidentially whether shares
held subject to the plan will be tendered in a tender or exchange offer; or
at or after that time, the business combination is approved by the board of directors and authorized at an
annual or special meeting of stockholders, and not by written consent, by the affirmative vote of at least 66
2/3% of the outstanding voting stock that is not owned by the interested stockholder.
Section 203 defines “business combination” to include the following:
•
•
•
•
•
any merger or consolidation of the corporation with the interested stockholder;
any sale, lease, exchange, mortgage, transfer, pledge or other disposition of 10% or more of the assets of
the corporation involving the interested stockholder;
subject to specified exceptions, any transaction that results in the issuance or transfer by the corporation of
any stock of the corporation to the interested stockholder;
any transaction involving the corporation that has the effect of increasing the proportionate share of the
stock of any class or series of the corporation beneficially owned by the interested stockholder; or
any receipt by the interested stockholder of the benefit of any loans, advances, guarantees, pledges, or other
financial benefits provided by or through the corporation.
2
In general, Section 203 defines an “interested stockholder” as any entity or person beneficially owning 15% or
more of the outstanding voting stock of the corporation and any entity or person affiliated with or controlling or
controlled by that entity or person.
The application of Section 203 may make it difficult and expensive for a third party to pursue a takeover
attempt that we do not approve, even if a change in control would be beneficial to the interests of our stockholders.
3
AMENDED AND RESTATED
LABORATORY CORPORATION OF AMERICA HOLDINGS
MASTER SENIOR EXECUTIVE SEVERANCE PLAN
(Effective January 1, 2021)
PURPOSE
The purpose of this Amended and Restated Laboratory Corporation of America Holdings
Master Senior Executive Severance Plan (the “Plan”) is to provide severance benefits for a select
group of management employees of Laboratory Corporation of America Holdings. The Plan is
intended to replace and consolidate the former Amended and Restated Laboratory Corporation of
America Holdings Master Senior Executive Severance Plan and the Amended Laboratory
Corporation of America Holdings Master Senior Executive Change in Control Severance Plan, both
originally effective February 10, 2009. The Plan is not intended to duplicate severance benefits
provided to certain employees who have entered into individual agreements relating to employment
or the termination thereof.
ARTICLE I
DEFINITIONS
When used in this Plan and initially capitalized, the following words and phrases shall have the
following meanings unless the context clearly requires otherwise:
1.1
“Base Salary” shall mean, as to any Covered Employee, the greatest of (1) the Covered
Employee’s annual base salary rate, as of the Covered Employees Qualifying Termination, (2) the
Covered Employee’s annual base salary rate as of the date the Covered Employee gives notice of a
valid Good Reason termination of employment, and (3) if the Covered Employee’s Qualifying
Termination occurs within 36 months following a Change in Control, the Covered Employee’s
annual base salary rate as of such Change in Control, in all cases, before reduction because of an
election between benefits or cash provided under a plan of the Company maintained pursuant to
Section 125 or 401(k) of the Internal Revenue Code of 1986, as amended, and before reduction for
any other amounts contributed to any other employee benefit plan.
1.2
“Cause” shall mean, as to any Covered Employee, that such Covered Employee shall
have committed prior to the Covered Employee’s termination of employment with the Company
any of the following acts:
(a)
an intentional act of fraud, embezzlement, theft, or any other material violation
of law in connection with his duties or in the course of his employment with the Company;
(b)
the conviction of or entering of a plea of nolo contendere to a felony;
(c)
alcohol intoxication on the job or current illegal drug use;
(d)
intentional wrongful damage to tangible assets of the Company;
(e)
intentional wrongful disclosure of material confidential information of the
Company and/or materially breaching the noncompetition, non-solicitation or confidentiality
provisions of any noncompetition, non-solicitation or confidentiality agreement, plan or policy
covering the activities of such Covered Employee;
(f)
knowing and intentional breach of any employment policy of the Company;
or
(g)
gross neglect or misconduct, disloyalty, dishonestly, or breach of trust in the
performance of the Covered Employee’s duties that is not corrected to the Company’s
satisfaction within 30 days of the Covered Employee receiving notice thereof.
1.3
“Change in Control” shall have the meaning given such term in the Company’s 2016
Omnibus Incentive Plan, as it may be amended from time to time, or any successor thereto.
1.4
corporation.
“Company” shall mean Laboratory Corporation of America Holdings and any successor
1.5
“Covered Employee” shall mean an employee described in ARTICLE II of the Plan.
1.6
“Designated Group” shall mean any one of the groups of employees designated as such
on Schedule I attached hereto.
1.7
“Effective Date” shall mean January 1, 2021.
1.8
“Good Reason” shall mean:
(a)
a material reduction in the base salary or targeted bonus as a percent of a base
salary without the consent of the Covered Employee;
(b)
relocation to an office location more than 75 miles from the Covered Employee’s
current office without the consent of the Covered Employee; or
(c)
a material reduction in job responsibilities and duties or transfer to another job
without the consent of the Covered Employee.
Notwithstanding the foregoing, “Good Reason” shall not include a reduction in base salary or target
bonus of the Covered Employee where such reduction is pursuant to a Company-wide reduction of
base salaries and/or target bonuses.
1.9
“Plan” shall mean this Amended and Restated Laboratory Corporation of America
Holdings Master Senior Executive Severance Plan, as the same may hereafter be amended from
time to time.
1.10
“Qualifying Termination” shall mean:
(a)
an involuntary Termination without Cause; or
(b)
a voluntary Termination with Good Reason; provided, however, that to constitute
a Qualifying Termination for Good Reason, (1) the Covered Employee must provide written
notice to the Company detailing the events that constitute Good Reason and the Covered
Employee’s desire to terminate the Covered Employee’s employment with the Company no
later than 30 days after the Covered Employee learns of the circumstances constituting Good
Reason, (2) the Company must fail to cure such circumstances within 30 days after receipt of
said notice (“Cure Period”), and (3) the Covered Employee must actually have a Termination
within 30 days after the end of said Cure Period. If the preceding procedures are not followed,
such Termination shall be considered a voluntary Termination without Good Reason and not a
Qualifying Termination.
Notwithstanding the foregoing, a “Qualifying Termination” shall not mean any Termination of a
Covered Employee’s employment with the Company by reason of death, disability, or retirement of
the Covered employee.
1.11
“Severance Pay” shall mean the sum payable as set forth in Section 3.1 of the Plan.
1.12
“MIB Average Bonus” shall mean the total dollar amount of the last three MIB
Bonuses paid to the Covered Employee divided by (3) three. If, however, (i) the Covered Employee
has received less than three MIB Bonuses during the term of the Covered Employee’s employment,
then the MIB Average Bonus shall equal the total dollar amount of the MIB Bonuses paid to the
Covered Employee divided by the number of MIB Bonuses received by the Covered Employee, and
(ii) if the Covered Employee has not received any MIB Bonuses during the term of the Covered
Employee’s employment, then the MIB Average Bonus shall equal the Covered Employee’s target
MIB Bonus for the year of the Covered Employee’s Qualifying Termination. In all cases, the total
dollar amount of an MIB Bonus paid to a Covered Employee who was employed for less than a full
MIB Bonus measurement period, shall be annualized.
1.13
“MIB Bonus” shall mean the annual cash incentive bonus paid to the Covered
Employee under the applicable annual cash incentive performance plan or program of the
Company.
1.14
“Term” shall mean the period commencing on the Effective Date and ending at the time
determined in accordance with Section 7.2.
1.15
“Termination” shall cover all terminations of employment referred to under this
Plan and shall mean a “separation from service” as defined in Section 409A of the Internal Revenue
Code of 1986, as amended (the “Code”) as amended.
ARTICLE II
COVERED EMPLOYEES
2.1
Status as a Covered Employee. Any management employee of the Company
designated by the Board to participate in the Plan and who is at the time of a Qualifying
Termination such a designated employee shall be eligible to receive the benefits described in the
Plan. As of the Effective Date, those employees so designated by the Board are as set forth on the
attached Schedule 1. No employee who is entitled to receive payments under an individual
agreement relating to benefits payable upon said employee’s termination of employment shall be
a Covered Employee, even if the employee’s position is listed on Schedule 1.
ARTICLE III
SEVERANCE PAY
3.1
Amount of Severance. Subject to Sections 3.2, 3.3, and 5.2, upon the occurrence
of a Qualifying Termination and the execution by the Covered Employee of a Special Severance
Agreement in substantially the form attached as Exhibit A (such agreement to be executed within
30 days of the Qualifying Termination or within 45 days of the Qualifying Termination if necessary
to comply with the requirements of the Age Discrimination in Employment Act of 1967), which
will contain, among other things, noncompetition, nonsolicitation, duty of loyalty, confidentiality,
and release provisions that shall apply to each severance arrangement during, and in certain
instances after, the time when any severance payments are being made to each Covered Employee,
the Company shall pay Severance Pay to a Covered Employee in an amount equal to the
mathematical product of multiplying the factor shown on Schedule 1 for the Designated Group to
which the Covered Employee belongs at the time of termination, times the sum of the Covered
Employee’s Base Salary plus MIB Average Bonus. Additionally, such Covered Employee shall be
entitled, for up to twelve months following a Qualifying Termination, to reimbursement by the
Company of the Applicable Premium for the continuation of those medical benefits, dental and
vision for which the Covered Employee qualified at the time of the Qualifying Termination,
pursuant to the Consolidated Omnibus Budget Reconciliation Act of 1985 (COBRA), to the extent
actually paid by the Covered Employee; provided, further, however, that any Section 125, health
flexible spending, dependent care and health savings account and similar plans are explicitly
excluded from the continuation of coverage provision of this section.
3.2
Effect on Other Benefit Programs.
(a)
The Severance Pay provided for hereunder is not intended to duplicate any payments
to which a Covered Employee would otherwise be entitled under any individual agreement relating
to employment (or the termination thereof) with the Company. Accordingly, no Severance Payment
shall be payable under the Plan to any employee of the Company who is a party to such an
agreement.
(b)
By the acceptance of any Severance Pay under the Plan, a Covered Employee shall
be deemed to waive, release, and forever discharge any and all claims to the payment of any
severance benefit under any employment contract, severance plan or program of the Company other
than the Plan.
3.3
Limitation on Amount of Severance Pay. Notwithstanding any other provision of this
Plan, the total of the Severance Pay plus the Applicable Premiums to be paid to or on behalf of a
Covered Employee shall not exceed three times the Covered Employee’s Annual Compensation
during the year immediately preceding the Covered Employee’s termination of service. “Annual
Compensation” means the amount represented in Box 1 of the Covered Employee’s W-2 for the
year immediately preceding the Covered Employee’s termination of service, annualized to the
extent the Covered Employee was not employed for a full year.
No Duty to Mitigate. A Covered Employee shall not be required by reason of the Plan to
3.4
mitigate damages or the amount of the Covered Employee’s Severance Pay under the Plan by
seeking other employment or otherwise, nor shall the amount of such payments be reduced or
adjusted by compensation earned by the Covered Employee as a result of employment after the
Covered Employee’s Qualifying Termination.
ARTICLE IV
CESSATION OF BENEFITS
4.1
Reemployment with the Company. A Covered Employee who recommences employment
with the Company but who has already received benefits under the Plan, or a predecessor thereto,
shall not be entitled to any further benefits under the Plan.
4.2
Breach of the Special Severance Agreement. If a Covered Employee breaches any
material term of the Special Severance Agreement, the Covered Employee shall be entitled to no
further benefits under the Plan. For purposes of this section, any violation of the confidentiality,
noncompetition, nonsolicitation, release, or duty of loyalty provisions of any plan, policy or
agreement of the Company shall be considered “material.”
ARTICLE V
DISTRIBUTION OF CASH PAYMENTS
Severance Pay. The Company shall pay the Covered Employee the amount to which the
5.1
Covered Employee is entitled under Section 3.1 as follows: (a) 50 percent of the total Severance
Pay due, less statutory deductions, shall be paid within 30 days following the execution of a Special
Severance Agreement, provided that if the calendar year in which the first installment of the
Severance Pay could be paid could vary depending on the time within which the Covered Employee
executes the Special Severance Agreement, payment will be made in the first payroll period in the
year following termination but after the Special Severance Agreement has become irrevocable; and
(b) the remaining 50 percent of Severance Pay, less statutory deductions, shall be paid within 30
days following the one-year anniversary of the execution of the Special Severance Agreement, but
only if the Covered Employee has complied in all material respects with the terms and conditions of
the Special Severance Agreement. Notwithstanding the foregoing, all payments due hereunder shall
be completed within 24 months of the termination of the Covered Employee’s employment, but
payments shall be due hereunder only if the Covered Employee has complied in all material
respects with the terms and conditions of the Special Severance Agreement.
Notwithstanding any provisions of this Plan to the contrary, if the Covered Employee is a “specified
employee” (within the meaning of Section 409A of the Code and determined pursuant to
procedures adopted by the Company) at the time of such Covered Employee’s Qualifying
Termination and if any portion of the payments or benefits to be received by the Covered Employee
upon a Qualifying Termination would be considered deferred compensation under Section 409A of
the Code, amounts that would otherwise be payable pursuant to this Plan during the six-month
period immediately following the Covered Employee’s Qualifying Termination (the “Delayed
Payments”) and benefits that would otherwise be provided pursuant to this Plan (the “Delayed
Benefits”) during the six-month period immediately following the Covered Employee’s Qualifying
Termination (such period, the “Delay Period”) shall instead be paid or made available on the
earlier of (i) the first business day of the seventh (7th) month following the date of the Covered
Employee’s Qualifying Termination or (ii) the Covered Employee’s death (the applicable date, the
“Permissible Payment Date”) if such a Delay Period is required to avoid the imposition of excise
taxes under Section 409A of the Code. If such a Delay Period is required, the Company shall also
reimburse the Covered Employee for the after-tax cost incurred by the Covered Employee in
independently obtaining any Delayed Benefits (the “Additional Delayed Payments”).
With respect to any amount of expenses eligible for reimbursement under Section 3.1 and
5.1, such expenses shall be reimbursed by the Company within thirty (30) calendar days following
the date on which the Company receives the applicable invoice from the Covered Employee but in
no event later than December 31 of the year following the year in which the Covered Employee
incurs the related expenses; provided, that with respect to reimbursement relating to the Additional
Delayed Payments, such reimbursement shall be made on the Permissible Payment Date. In no
event shall the reimbursements or in-kind benefits to be provided by the Company in one taxable
year affect the amount of reimbursements or in-kind benefits to be provided in any other taxable
year, nor shall the Covered Employee’s right to reimbursement or in-kind benefits be subject to
liquidation or exchange for another benefit.
It is the intention of the parties that payments or benefits payable under this Plan not be
subject to the additional tax imposed pursuant to Section 409A of the Code. To the extent such
potential payments or benefits could become subject to such Section, the Company may amend this
Plan with the goal of giving the Covered Employee the economic benefits described herein in a
manner that does not result in such tax being imposed.
For purposes of Section 409A of the Code, a Covered Employee’s right to receive any
“installment” payments pursuant to this Plan shall be treated as a right to receive a series of separate
and distinct payments.
For purposes of this Section 5.1, “Separation from Service” has the meaning provided
under Section 409A of the Code.
5.2
Section 280G of the Code. Notwithstanding the application of the calculation of benefits
hereunder, in the event that the payments or distributions to be made by the Company to or for the
benefit of the Covered Employee (whether paid or payable or distributed or distributable pursuant
to the terms of this Plan, under some other plan, agreement, or arrangement, or otherwise) (a
“Payment”) constitute “parachute payments” within the meaning of Section 280G of the Code, then
the Payment to the Covered Employee shall be subject to the terms of Section 17 (“Parachute
Provisions”) of the Company’s 2016 Omnibus Incentive Plan, as it may be amended from time to
time, or any successor thereto.
ARTICLE VI
ADMINISTRATION OF PLAN
In General: Delegation. The Plan shall be administered by the Board. The Board shall have
6.1
sole and absolute discretion to interpret where necessary all provisions of the Plan (including,
without
correcting deficiencies
supplying omissions
limitation, by
from,
in, or
resolving inconsistencies or ambiguities in, the language of the Plan), to determine the rights and
status under the Plan of employees or other persons, to resolve questions or disputes arising under
the Plan, and to make any determinations with respect to the benefits payable hereunder and the
persons entitled thereto as may be necessary for the purposes of the Plan. Without limiting the
generality of the foregoing, the Board is hereby granted the authority (i) to determine whether a
particular termination of employment constitutes a “Qualifying Termination,” and (ii) to
determine whether a particular employee is a “Covered Employee” under the Plan.
The Board may delegate any of its administrative duties, including, without limitation,
duties with respect to the processing, review, investigation, approval, and payment of Severance
Pay to a named administrator or administrators. The Board’s determination of the rights of any
employee hereunder shall be final and binding on all persons.
6.2
Regulations. The Board may promulgate any rules and regulations that it deems necessary
to carry out the purposes of this Plan, or to interpret the terms and conditions of the Plan; provided,
however, that no rule, regulation, or interpretation shall be contrary to the provisions of the Plan.
The rules, regulations, and interpretations made by the Board, and any determination of entitlement
to benefits hereunder, shall be final and binding on any employee or former employee of the
Company.
6.3
Claims for Benefits and Review of Denials. A terminating Covered Employee will be
considered for benefits under the Plan automatically. Any other employee of the Company who
believes such employee is entitled to a benefit under the Plan may make a claim for such benefit by
submitting a written statement to the Executive Vice President and Chief Human Resource Officer
setting forth the benefit to which the claimant deems himself/herself entitled, and the factual basis
for such employee’s claim.
The Board of Directors or its delegate (hereinafter “Board of Directors” for purposes of
Section 6.3 only) will make a determination of whether an employee recognized by the Board of
Directors as a Covered Employee is entitled to benefits under this Plan no later than the day prior to
the date of such employee’s termination. The Board of Directors will act on any other application
(including a claim of status as a Covered Employee made as part of a claim for benefits) or make
any other determination it is requested to make under the Plan and will inform the employee of its
decision within 30 days of the date the application or request is made, unless a longer time is
required by special circumstances, in which event the claimant will be notified in writing of the
special circumstances and of the expected decision date. The determination will be made no later
than 90 days after the date the application or request is received. If the determination is a denial of a
claim, the Board of Directors will notify the claimant in writing of the denial, setting forth the
specific reasons for the denial and referring specifically to the Plan provisions on which the denial
is based. The notice also will contain a description of any additional material or information
necessary for the claimant to perfect the claim and an explanation of why such material is
necessary. The notice will provide appropriate information to the claimant on steps to appeal the
denial. The claimant will have 60 days from the date of the notice to request review of the decision
by the Board of Directors and may review pertinent documents and submit any additional
information along with the request for review that the employee deems pertinent. A decision on
review will be made within 60 days of receipt of the request for review, except that the time for
rendering the decision may be extended to 120 days when special circumstances make it necessary
to do so, in which event the claimant will be notified in writing of the extension, informed of the
special circumstances, and informed of an expected decision date. The decision on review, if it is a
denial of the claim, will be in writing, will specify the provisions of the Plan on which it is based,
and will set forth specific reasons for the denial.
ARTICLE VII
AMENDMENT OR TERMINATION OF PLAN
7.1
Right to Amend or Terminate. The Company reserves the right to alter, amend, or
terminate the Plan at any time. Any change in the terms of the Plan (including termination of the
Plan) that results from the exercise of the Company’s right to alter, amend, or terminate the Plan
may be applicable to active and/or former employees, including employees who separated from
service prior to the date on which the Company exercises its power to alter, amend, or terminate the
Plan, provided, however, that no such change in the terms of the Plan will affect the amount of any
benefit that was paid prior to the date on which such change is adopted, or any benefit promised in a
Special Severance Agreement that was fully executed prior to the date on which such change is
adopted. Only the Board of Directors may exercise the Company’s reserved rights under this
paragraph. No officer, employee, or representative of the Company has the authority to promise or
represent that anyone’s coverage and/or benefit under the Plan is or will be exempt from the
Company’s reserved right to alter, amend, or terminate the Plan at any time. Notwithstanding the
foregoing, in the event of a Change in Control while the Plan is in effect, the Plan and a Covered
Employee’s participation in the Plan shall not be terminated for 36 months following such Change
in Control.
Termination. This Plan shall continue in force until such time as the Board shall terminate
7.2
the Plan, subject to the limitations set forth in Section 7.1.
ARTICLE VIII
METHOD OF FUNDING
8.1
Plan is Not Funded. The Company shall pay benefits under the Plan from current operating
funds. No property of the Company is or shall be, by reason of this Plan, held in trust for any
employee of the Company, nor shall any person have any interest in or any lien or prior claim upon
any property of the Company by reason of this Plan or the Company’s obligations to make
payments hereunder.
ARTICLE IX
MISCELLANEOUS
Limitation on Rights. Neither the establishment of the Plan nor participation herein shall
9.1
give any employee the right to be retained in the service of the Company or any rights to any
benefits whatsoever, except to the extent specifically set forth herein.
9.2 Headings. Headings of Articles and Sections in this instrument are for convenience only
and do not constitute any party of the Plan.
Tax Withholding. The Company may withhold from any amounts payable under this Plan
9.3
all federal, state, city, or other taxes as shall be required to be withheld pursuant to any law or
governmental regulation or ruling.
Governing Law. The Plan shall be construed and governed in all respects in accordance with the
internal substantive laws of the State of Delaware.
The undersigned authorized officer of the Company has executed this document on the 31st
day of December, 2020.
LABORATORY CORPORATION OF
AMERICA HOLDINGS
By: /s/ Sandra D. van der Vaart
Sandra D. van der Vaart
Executive Vice President and Chief Legal
Officer
Schedule 1 to
Amended and Restated Master Senior Executive Severance Plan
Designated Groups, Covered Employees,
and Benefit Levels
Designated
Group
Covered
Employees
Severance Benefit as
a Multiple of Base
Salary Plus MIB
Average Bonus
Executive Vice
Presidents
All Executive Vice
Presidents
Senior Vice
Presidents
All Senior Vice
Presidents
2X
1X
Exhibit A
Special Severance Agreement
DATE
Re: Employment Separation Agreement and General Release
Dear______________,
On behalf of Laboratory Corporation of America Holdings (the “Company”), I write to
offer you (the “Employee”) the following Employment Separation Agreement and General Release
(the “Agreement”).
1.0
Termination of Employment
1.1
Effective _____________(the “Termination Date”), Employee’s employment
with the Company was terminated; he/she shall perform no further services for the Company
and his/her status as an employee and Officer of the Company shall cease on that date.
Employee and the Company further agree that the relationship created by this Agreement is
purely contractual and that no employer-employee relationship is intended, nor shall such be
inferred from the performance of obligations under this Agreement. Employee further
agrees that any payments and/or benefits payable pursuant to this Agreement are contingent
upon Employee’s execution and fulfillment of his/her obligations under this Agreement.
2.0
Separation Pay
2.1
In consideration for the covenants, promises and agreements herein and in
particular Employee’s release of claims as well as covenants not to solicit, not to compete
and not to disclose confidential information, the Company will pay Employee a severance in
the total amount of $___, less applicable taxes and withholdings (hereafter referred to
as “Severance Pay”), which equals the Employee’s Base Salary of $_____ plus Employee’s
MIB Average Bonus as defined in the Plan of $_________. The severance shall be paid in
two installments, with the first installment of $_________, less taxes and withholding, made
payable within 30 days following the Termination Date and the second installment of
$____, less taxes and withholding, made payable within 30 days following the one-year
anniversary of the Termination Date.
2.2
The Company shall not be responsible for making any payment under this
Section 2.0 and its sub-parts if Employee has not complied in all material respects with the
terms and conditions of this Agreement.
3.0
Benefits
3.1
Employee, his/her spouse, and his/her other dependent(s) may be eligible to
elect continued health care coverage under the welfare plans sponsored by the Company, as
provided in the applicable provisions of the Consolidated Omnibus Budget
Reconciliation Act of 1985, as amended (“COBRA”), which provides generally that certain
employees and their dependents may elect to continue coverage under employer- sponsored
group health plans for a period of at least eighteen (18) months under certain conditions,
including payment by Employee of the “Applicable Premium” as defined in Section 604 of
the Employee Retirement Income Security Act of 1974, as amended, 29 U.S.C. §§ 1001 et
seq. (“ERISA”). In the event Employee elects continuation of coverage under COBRA for
himself/herself and his/her spouse and dependents, the Company will pay the Applicable
Premium for such coverage (medical, dental, optical and prescription coverage for spouse
and dependents) for 12 months, thereof. To be clear, the COBRA reimbursement will not
include the Applicable Premium for any Section 125, health flexible spending, dependent
care and health savings account and similar plans. Employee shall be responsible for, and
will be required to pay, the Applicable Premium for any COBRA coverage beyond the 12
month period.
3.2
Employee shall be eligible for such benefits under the Company’s existing
qualified plans as are provided under the circumstances (taking into account termination of
employment as of the Termination Date) pursuant to the terms of the plan documents
governing each of these plans. Except as otherwise provided herein or in the terms of any
documents governing any employee benefit plan maintained by the Company, Employee
will cease to be a participant in and will no longer have any coverage or entitlement to
benefits, accruals, or contributions under any of the Company’s employee benefit plans
effective upon the termination of his/her employment. Employee agrees that the payments
made to him/her by the Company pursuant to this Agreement do not constitute
compensation for purposes of calculating the amount of benefits that Employee may be
entitled to under the terms of any pension plan or for the purposes of accruing any benefit,
receiving any allocation of any contribution, or having the right to defer any income in any
profit-sharing or other employee pension benefit plan, including any cash or deferred
arrangement.
3.3
Employee also understands that his/her equity awards are governed by the
terms and conditions of the Company’s 2016 Incentive Stock Plan and Omnibus Incentive
Plan or predecessor plans and individual equity award agreements. Nothing in this
Agreement alters, changes, or amends the terms and conditions of said equity awards and
award agreements.
3.4
Employee shall submit for reimbursement any and all unpaid business
expenses to the Company within 30 days of the Termination Date. The Company will
reimburse said expenses provided that they are consistent with, and reimbursable under, the
Company’s travel and entertainment expense policy. The Company will not be responsible
for reimbursing the Employee for any business expenses submitted after said 30 day period.
3.5
This Agreement shall never be construed as an admission by the Company of
any liability, wrongdoing or responsibility on its part or on the part of any other person or
entity described in Section 4.1 of this Agreement. The Company expressly denies any such
liability, wrongdoing or responsibility.
4.0
Release
4.1
Employee, on behalf of himself/herself and his/her heirs, assigns, transferees
and representatives, hereby releases and forever discharges the Company, and its
predecessors, successors, parents, subsidiaries, affiliates, assigns, representatives and agents,
as well as all of their present and former directors, officers, employees, agents, shareholders,
representatives, attorneys and insurers (collectively, the “Releasees”), from any and all
claims, causes of actions, demands, damages or liability of any nature whatsoever, known or
unknown, which Employee has or may have which arise out of his/her employment or
cessation of employment with the Company, or which concern or relate in any way to any
acts or omissions done or occurring prior to and including the date of this Agreement,
including, but not limited to, claims arising under the Fair Labor Standards Act; the Equal
Pay Act; Title VII of the Civil Rights Act of 1964; 42 U.S.C.§ 1981 et seq.; the Americans
with Disabilities Act; the Family and Medical Leave Act; the Employee Retirement Income
Security Act of 1974; the Worker Adjustment and Retraining Notification Act, the Age
Discrimination in Employment Act; the Genetic Information Nondiscrimination Act of 2008
(GINA), any and all claims for discrimination, wrongful termination and/or retaliation;
claims for breach of contract, express or implied; claims for breach of the covenant of good
faith and fair dealing; claims for compensation, including but not limited to wages, bonuses,
or commissions except as otherwise contained herein; claims for benefits or fringe benefits,
including, but not limited to, claims for severance pay and/or termination pay, except as
otherwise contained herein; claims for, or relating to stock or stock options (except that
nothing in this Agreement shall prohibit Employee from exercising any vested stock options
or affect Employee’s claims to vested benefits in the Company’s Employees’ Retirement
Savings Plan, Deferred Compensation Plan, Employee Stock Purchase Plan, or Cash
Balance Retirement Plan, in accordance with the terms of the applicable stock option
agreement(s) and applicable plan documents); claims for unaccrued vacation pay; claims
arising in tort, including, but not limited to, claims for invasion of privacy, negligent or
intentional infliction of emotional distress, fraud, negligent or intentional misrepresentation,
and defamation; claims for quantum meruit and/or unjust enrichment; and any and all other
claims arising under any other federal, state, local or foreign laws, as well as any and all
other common law legal or equitable claims.
4.2
Employee represents that he/she has not initiated any action or charge against
any of the Releasees with any Federal, State or local court or administrative agency.
Employee knowingly and intentionally waives any rights to any additional recovery that
might be sought on his/her behalf by any other person, entity, local, state or federal
government or agency thereof, including specifically and without limitation, the United
States Department of Labor, the Equal Employment Opportunity Commission and
comparable State agencies.
4.3
Employee is hereby advised that: (i) he/she should consult with an attorney
(at his/her own expense) prior to executing this Agreement; (ii) he/she is waiving, among
other things, any age discrimination claims under the Age Discrimination in Employment
Act, provided, however, he/she is not waiving any claims that may arise after the date this
Agreement is executed; (iii) he/she has twenty-one (21) days within which to consider the
execution of this Agreement, before signing it; and (iv) for a period of seven (7) days
following the execution of this Agreement, he/she may revoke this Agreement by delivering
written notice (by the close of business on the seventh day) to the Company in accordance
with Section 10.7 herein.
4.4
Notwithstanding the provisions of Section 4.1, said release does not apply to
any and all statutory or other claims that are prohibited from waiver by Federal, State or
local law.
4.5
The parties agree that the Company has no prior legal obligation to make the
additional payments set forth above in Sections 2.0 and 3.0 (including the sub-parts thereto)
and that it has been exchanged for the promises of Employee stated in this Agreement. It is
specifically understood and agreed that the additional payments, and each of them, are good
and adequate consideration to support the waivers, releases and obligations contained
herein, including, without limitation, Sections 4.0, 5.0, 6.0, 7.0, and 8.0, and their respective
sub-parts, and that all of the payments set forth Sections 2.0 and 3.0 (including the sub-parts
thereto) are of value in addition to anything to which Employee already was entitled prior to
the execution of this Agreement.
5.0
Confidentiality
5.1
Employee understands and agrees that all discussions, negotiations and
correspondence relating to this Agreement as well as the terms of this Agreement are strictly
confidential and agrees not to disclose to anyone (other than counsel, accountants,
immediate family members) such information except as otherwise permitted under Section
5.7.
5.2
The parties acknowledge that during the course of Employee’s employment
with the Company, he/she was given access, on a confidential basis, to Confidential
Information which the Company has for years collected, developed, and/or discovered
through a significant amount of effort and at great expense. The parties acknowledge that
the Confidential Information of the Company is not generally known or easily obtained in
the Company’s trade, industry, business, or otherwise and that maintaining the secrecy of
the Confidential Information is extremely important to the Company’s ability to compete
with its competitors.
5.3
Employee agrees that for a period of seven (7) years from the date of this
Agreement, Employee shall not, without the prior written consent of the Company, divulge
to any third party or use for his/her own benefit, or for any purpose other than the exclusive
benefit of the Company, any Confidential Information of the Company; provided however,
that nothing herein contained shall restrict Employee’s ability to make such disclosures as
such disclosures may be required by law; and further providing that nothing herein
contained shall restrict Employee from divulging information that is readily available to the
general public as long as such information did not become available to the general public as
a direct or indirect result of Employee’s breach of this section of this Agreement.
5.4
The term “Confidential Information” in this Agreement shall mean
information that is not readily and easily available to the public or to persons in the same
business, trade, or industry of the Company, and that concerns the Company’s prices,
pricing methods, costs, profits, profit margins, suppliers, methods, procedures, processes or
combinations or applications thereof developed in, by, or for the Company’s business,
research and development projects, data, business strategies, marketing strategies, sales
techniques, customer lists, customer information, or any other information concerning the
Company or its business that is not readily and easily available to the public or to those
persons in the same business, trade, or industry of the Company. The term “customer
information” as used in this Agreement shall mean information that is not readily and easily
available to the public or to those persons in the same business, trade, or industry and that
concerns the course of dealing between the Company and its customers or potential
customers solicited by the Company, customer preferences, particular contracts or locations
of customers, negotiations with customers, and any other information concerning customers
obtained by the Company that is not readily and easily available to the public or to those in
the business, trade, or industry of the Company.
5.5
Employee acknowledges that all information, the disclosure of which is
prohibited hereby, is of a confidential and proprietary character and of great value to the
Company, and upon the execution of this Agreement (or as soon thereafter as is reasonably
practicable), Employee shall forthwith deliver up to the Company all records, memoranda,
data, and documents of any description that refer to or relate in any way to such information
and shall return to the Company any of its equipment and property which may then be in
Employee’s possession or under Employee’s personal control.
5.6
Employee hereby agrees that any failure to fully and completely comply with
this provision shall entitle the Company to seek damages for a demonstrated breach of the
confidentiality provision, to include recoupment of monies paid hereunder.
5.7
Notwithstanding the restrictions set forth in Section 5.0 and its subparts,
Employee may disclose information protected under Section 5.0 and its subparts if and only
if such is (i) lawfully required by any government agency; (ii) otherwise required to be
disclosed by law (including legally required financial reporting) and/or by court order; (iii)
necessary in any legal proceeding in order to enforce any provision of this Agreement or (iv)
made to the Securities Exchange Commission regarding security law issues or other
government agency regarding a regulatory matter. Employee further agrees that he/she will
notify the Company in writing within five (5) calendar days of the receipt of any subpoena,
court order, administrative order or other legal process requiring disclosure of information
subject to Section 5.0 and sub-parts thereto. Employee may also disclose the contents of
Section 6.0 and its sub-parts and only those contents to any subsequent employer.
6.0
Non-Solicitation/Non-Compete
6.1
For a period of twelve (12) months the Termination Date, Employee shall not
become an owner in, shareholder with more than a 2% equity interest in, investor in, or an
employee, contractor, consultant, advisor, representative, officer, director, or agent
of, a trade or business that offers products and services that are the same or substantially
similar to the products and services provided by the Employer Company in any geographic
market in which the Employer Company conducts business (“Competitor”); provided,
however, that the duties and responsibilities of said employment or engagement as an owner
in, shareholder with more than 2% equity interest in, investor in, contractor, consultant,
advisor, representative, officer, director or agent are (i) the same, similar, or substantially
related to current duties and responsibilities or duties or responsibilities performed by
Employee while employed by the Company at any time during a six (6) month period prior
to Termination Date and (ii) related to or concerning the Competitor’s business activities in
the Restricted Territory. The parties agree and affirm that their intention with respect to
Section 6.1 is that Employee’s activities shall be limited only for the twelve (12) month
period after the separation of employment for any reason. The provisions calling for a "look
back" of six (6) calendar months prior to the separation of employment are intended solely
as a means of identifying the duties and responsibilities that will define the restricted
activities covered by Section 6.1 and are not intended to nor shall they, under any
circumstances, be construed to define the length or term of any such restriction. For
purposes of Section 6.1, the term “Restricted Territory” means the geographic area that was
part of Employee’s duties and responsibilities within a period of six (6) month period prior
to the date of your termination of employment. If a court of competent jurisdiction
determines that the Restricted Territory as defined herein is too restrictive, then the parties
agree that said court may reduce or limit the Restricted Territory to the largest acceptable
area so as to enable the enforcement of Section 6.1.
6.2
For a period of twelve (12) months following the Termination Date,
Employee will not, either directly or indirectly, or on behalf of any person, business,
partnership, or other entity, call upon, contact, or solicit any customer or customer prospect
of the Company, or any representative of the same, with a view toward the sale or providing
of any service or product competitive with the Company’s Business; provided, however, the
restrictions set forth in this Section shall apply only to customers or prospects of the
Company, or representatives of the same, with which during the past 12 month period the
Employee had contact or who were known by Employee to be customers or prospects, or
representatives of the same, of the Company. The parties agree and affirm that their
intention with respect to Section 6.2 of this Agreement is that Employee's activities be
limited only for a twelve (12) month period after the Termination Date for any reason. The
provisions calling for a "look back" of 12 calendar months prior to the Termination Date are
intended solely as a means of identifying the clients to which such restrictions apply and are
not intended to nor shall they, under any circumstances, be construed to define the length or
term of any such restriction.
6.3
For a period of twelve 12 months following the Termination Date, Employee
shall not directly or indirectly through a subordinate, co-worker, peer, or any other person or
entity contact, solicit, encourage or induce any officer, director or employee of the Company
or its subsidiary companies to work for or provide services to Employee and/or any other
person or entity.
6.4
Employee acknowledges and agrees that the foregoing restrictions are
necessary for the reasonable and proper protection of the Company; are reasonable in
respect to subject matter, length of time, geographic scope, customer scope, and scope of
activity to be restrained; and are not unduly harsh and oppressive so as to deprive Employee
of his/her livelihood or to unduly restrict Employee’s opportunity to earn a living after
termination of Employee’s employment with the Company. Employee further acknowledges
and agrees that if any restrictions set forth in this Section are found by any court of
competent jurisdiction to be unenforceable or otherwise against public policy, the restriction
shall be interpreted to extend only over the maximum period of time or other restriction as
to which it would otherwise be enforceable.
6.5
Employee acknowledges and agrees that because the violation, breach, or
threatened breach of this Section and its sub-parts would result in immediate and irreparable
injury to the Company, the Company shall be entitled, without limitation of remedy, to (a)
temporary and permanent injunctive and other equitable relief restraining Employee from
activities constituting a violation, breach or threatened breach of this Section and its sub-
parts to the fullest extent allowed by law; (b) all such other remedies available at law or in
equity, including without limitation the recovery of damages, reasonable attorneys’ fees and
costs; and (c) withhold any further rights, payments or benefits under this Agreement which
become due and owing after the occurrence of said violation, breach, or threatened breach,
including, without limitation, any rights or claims under Sections 2.0 and 3.0 and the sub-
parts thereto.
7.0
Return of Company Property
7.1
Employee agrees that within 10 days after execution of this Agreement, he/
she will return any and all Company documents and any copies thereof, in any form
whatsoever, including computer records or files, containing secret, confidential and/or
proprietary information or ideas, and any other Company property (including, but not
limited to, any cell phones, laptops, notepads, ipads, printers and/or other computer
equipment) in Employee’s possession or control.
8.0
Duty to Cooperate and of Loyalty/Nondisparagement
8.1 Without limitation as to time, Employee agrees to cooperate and make all
reasonable and lawful efforts to assist the Company in addressing any issues which may
arise concerning any matter with which he/she was involved during his/her employment
with the Company, including, but not limited to cooperating in any litigation arising
therefrom. Employee will also be compensated for expenses directly incurred solely in
connection with such services, provided however that the expenses are both fair and
reasonable and consistent with Company policy on expense reimbursement. For avoidance
of doubt, expenses directly incurred solely in connection such services would include
expenses such as travel, photocopying or other expense incurred solely for the benefit of the
Company but would not include such indirect and overhead expenses such as but not limited
to phone, computer, internet, office supplies, or rent.
8.2
Employee will not (except as required by law) communicate to anyone,
whether by word or deed, whether directly or through any intermediary, and whether
expressly or by suggestion or innuendo, any statement, whether characterized as one of
fact or of opinion, that is intended to cause or that reasonably would be expected to cause
any person to whom it is communicated to have (1) a lowered opinion of the Company or
any affiliates, including a lowered opinion of any products manufactured, sold, or used by,
or any services offered or rendered by the Company or its affiliates; and/or (2) a lowered
opinion of the Company’s creditworthiness or business prospects. Employee’s obligation in
this regard extends to the reputation of the Company and any other person or entity
described in Section 4.1 of this Agreement. This Section shall not be construed as
prohibiting the Employee from communicating truthful information (a) in response to
assistance requested under Section 8.1 of this Agreement, (b) in any formal or informal
proceeding with a government agency or investigator, (c) any litigation against the
Company including, but not limited to, qui tam lawsuits whether the government decides to
intervene or declines to intervene and the relator moves forward pursuing its claims, (d) as
required by law, such as in response to a duly-issued subpoena, or (e) any action to enforce
the terms of this Agreement or right not waived under Section 4.0 and subparts thereunder.
9.0
Section 409A of the Code
9.1
Notwithstanding any provisions of this Agreement to the contrary, if the
Employee is a “specified employee” (within the meaning of Section 409A of the Internal
Revenue Code of 1986, as amended (the “Code”) and determined pursuant to procedures
adopted by the Company) at the Termination Date and if any portion of the payments or
benefits to be received by the Employee would be considered deferred compensation under
Section 409A of the Code, amounts that would otherwise be payable pursuant to this
Agreement during the six-month period immediately following the Employee’s Termination
Date (the “Delayed Payments”) and benefits that would otherwise be provided pursuant to
this Agreement (the “Delayed Benefits”) during the six-month period immediately
following the Employee’s Termination Date (such period, the “Delay Period”) shall instead
be paid or made available on the earlier of (i) the first business day of the seventh (7th)
month following the Termination Date or (ii) the Employee’s death (the applicable date, the
“Permissible Payment Date”). The Company shall also reimburse the Employee for the
after-tax cost incurred by the Employee in independently obtaining any Delayed Benefits
(the “Additional Delayed Payments”).
9.2 With respect to any amount of expenses eligible for reimbursement under
Sections 3.1, 3.4 and 9.1, such expenses shall be reimbursed by the Company within thirty
(30) calendar days following the date on which the Company receives the applicable invoice
from the Employee but in no event later than December 31 of the year following the year in
which the Employee incurs the related expenses; provided, that with respect to
reimbursement relating to the Additional Delayed Payments, such reimbursement shall be
made on the Permissible Payment Date. In no event shall the reimbursements or in-kind
benefits to be provided by the Company in one taxable year affect the amount of
reimbursements or in-kind benefits to be provided in any other taxable year, nor shall the
Employee’s right to reimbursement or in-kind benefits be subject to liquidation or exchange
for another benefit.
9.3
It is the intention of the parties that payments or benefits payable under this
Agreement not be subject to the additional tax imposed pursuant to Section 409A of the
Code. To the extent such potential payments or benefits could become subject to such
Section, the Company may amend this Agreement with the goal of giving the Covered
Employee the economic benefits described herein in a manner that does not result in such
tax being imposed.
9.4
For purposes of Section 409A of the Code, an Employee’s right to receive
any “installment” payments pursuant to this Agreement shall be treated as a right to receive
a series of separate and distinct payments.
10.0 Miscellaneous
10.1 This Agreement is binding on, and shall inure to the benefit of, the Parties
hereto and their heirs, representatives, transferees, principals, executors, administrators,
predecessors, successors, parents, subsidiaries, affiliates, assigns, agents, directors, officers
and employees.
10.2 The Plan is incorporated herein by reference. This Agreement constitutes the
complete agreement between, and contains all of the promises and undertakings by the
Parties. Employee agrees that the only considerations for signing this Agreement are the
terms stated herein above and that no other representations, promises, or assurances of any
kind have been made to him by the Company, its attorneys, or any other person as an
inducement to sign this Agreement. Any and all prior agreements, representations,
negotiations and understandings among the Parties, oral or written, express or implied, with
respect to the subject matter hereof are hereby superseded and merged herein.
10.3 This Agreement may not be revised or modified without the mutual written
consent of the Parties.
10.4 The Parties acknowledge and agree that they have each had sufficient time to
consider this Agreement and consult with legal counsel of their choosing concerning its
meaning prior to entering into this Agreement. In entering into this Agreement, no Party has
relied on any representations or warranties of any other Party other than the representations
or warranties expressly set forth in this Agreement. Employee acknowledges that he/she has
read this Agreement and that he/she possesses sufficient education and experience to fully
understand the terms of this Agreement as it has been written, the legal and binding effect of
this Agreement, and the exchange of benefits and payments for promises hereunder, and that
he/she has had a full opportunity to discuss or ask questions about all such terms.
10.5 Except as otherwise provided in this Section, if any provision of this
Agreement shall be determined to be invalid or unenforceable by a court of competent
jurisdiction, that part shall be ineffective to the extent of such invalidity or unenforceability
only, without in any way affecting the remaining parts of said provision or the remaining
provisions of this Agreement; provided that, if any provision contained in this Agreement
shall be adjudicated to be invalid or unenforceable because such provision is held to be
excessively broad as to duration, geographic scope, activity or subject, such provision shall
be deemed amended by limiting and reducing it so as to be valid and enforceable to the
maximum extent compatible with the applicable laws of such jurisdiction, and such
amendment only to apply with respect to the operation of such provision in the applicable
jurisdiction in which the adjudication is made. If as a result of litigation brought by the
Employee or as a result of any defense asserted by the Employee Section 6.0 or any of its
sub-parts of this Agreement is deemed invalid or unenforceable, in whole or in part, by a
court of competent jurisdiction, this entire Agreement shall be null and void, and any
consideration paid hereunder shall be repaid immediately by Employee upon receipt of
notice thereof.
10.6 Employee agrees that because he/she has rendered services of a special,
unique, and extraordinary character, damages may not be an adequate or reasonable remedy
for breach of his/her obligations under this Agreement. Accordingly, in the event of a breach
or threatened breach by Employee of the provisions of this Agreement, the Company shall
be entitled to (a) an injunction restraining Employee from violating the terms hereof, or
from rendering services to any person, firm, corporation, association, or other entity to
which any confidential information, trade secrets, or proprietary materials of the Company
have been disclosed or are threatened to be disclosed, or for which Employee is working or
rendering services, or threatens to work or render services (b) all such other remedies
available at law or in equity, including without limitation the recovery of damages,
reasonable attorneys’ fees and costs, and (c) withhold any further payments under this
Agreement which become due and owing after the occurrence of said violation, breach or
threatened breach. Nothing herein shall be construed as prohibiting the Company from
pursuing any other remedies available to it for such breach or threatened breach of this
Agreement, including the right to terminate any payments to Employee pursuant to this
Agreement or the recovery of damages from Employee. Employee agrees that the issuance
of the injunction described in this Section may be without the posting of any bond or other
security by the Company.
10.7 Such notice and any other notices required under this Agreement shall be
served upon the Company by certified mail, return receipt requested, or by expressed
delivery by a nationally recognized delivery service company such as Federal Express as
follows:
If to the Company:
Laboratory Corporation of America Holdings 531 S. Spring Street
Burlington, NC 27215
Telephone No.: (336) 436-4226
Telecopier No.: (336) 436-4177 Attention: EVP, Chief Legal Officer
With a copy to:
Laboratory Corporation of America Holdings 531 S. Spring Street
Burlington, NC 27215
Attention: Director of HR Compliance
Consistent with the requirements of this Section, each party shall notify the other
party of any change of address for the receipt of a notice under this Agreement.
10.8 This Agreement shall be construed in accordance with and governed by the
laws, except choice of law provisions, of the State of North Carolina and shall govern to the
exclusion of the laws of any other forum including but not limited to the laws of the State of
California. The parties further agree that any action, special proceeding or other proceeding
with respect to this Agreement shall be brought exclusively in the federal or state courts of
the State of North Carolina. Employee and Company irrevocably consent to the
jurisdiction of the Federal and State courts of North Carolina and that Employee hereby
consents and submits to personal jurisdiction in the State of North Carolina. Employee
and Company irrevocably waive any objection, including an objection or defense based on
lack of personal jurisdiction, improper venue or forum non-conveniens which either may
now or hereafter have to the bringing of any action or proceeding in connection with this
Agreement. Employee acknowledges and recognizes that in the event that he/she has
breached this Agreement, the Company may initiate a lawsuit against him/her in North
Carolina, that Employee waives his/her right to have that lawsuit be brought in a court
located closer to where he/she may reside, and that Employee will be required to travel to
and defend himself/herself in North Carolina.
The Effective Date of this Agreement shall be either (a) the Termination Date or (b) the day after
expiration of the seven (7) day revocation period set forth in Section 4.3 of this Agreement,
whichever date is later.
If you agree with the foregoing, please sign below and return two (2) originals to me. You
should retain one (1) original copy of this Agreement for your records.
Sincerely,
Agreed to and accepted:
Date:
Exhibit 21 LIST OF SUBSIDIARIES
1957285 Ontario Inc. dba Quality Underwriting Services
2089729 Ontario, Inc.
2248848 Ontario Inc.
3065619 Nova Scotia Company
3257959 Nova Scotia Company
896988 Ontario Limited
9279-3280 Quebec Inc.
Accupath Diagnostic Laboratories, Inc.
Alpha Medical Laboratory LLC
Beacon LBS IPA, Inc.
Beacon Laboratory Benefit Solutions, Inc.
CannAmm GP Inc.
CannAmm Limited Partnership
Center for Disease Detection International
Center for Disease Detection, LLC
Centrex Clinical Laboratories, Inc.
Clearstone Central Laboratories (U.S.) Inc.
Clearstone Holdings (International) Ltd.
Clipper Holdings, Inc.
Colorado Coagulation Consultants, Inc.
Colorado Laboratory Services, LLC
Correlagen Diagnostics, Inc.
Covance Inc.
Curalab Inc.
Cytometry Associates, Inc.
Czura Thornton (Hong Kong) Limited
DCL Acquisition, Inc.
DCL Medical Laboratories, LLC (FL)
DCL Medical Laboratories, LLC (DE)
DCL Sub LLC
Decision Diagnostics, L.L.C. (aka DaVinici/Medicorp LLC)
Diagnostic Services, Inc.
DIANON Systems, Inc.
DL Holdings Limited Partnership
Dynacare - Gamma Laboratory Partnership
Dynacare Company
Dynacare G.P. Inc.
Dynacare Holdco LLC
Dynacare Laboratories Inc.
Dynacare Laboratories Limited Partnership
Dynacare Northwest Inc.
Dynacare Realty Inc.
DynaLifeDX
DynalifeDX Infrastructure Inc.
Endocrine Sciences, Inc.
Esoterix Genetic Counseling, LLC
Esoterix Genetic Laboratories, LLC
Esoterix, Inc.
Execmed Health Services Inc.
FirstSource Laboratory Solutions, Inc.
Gamma Dynacare Central Medical Laboratories GP Inc.
Gamma Dynacare Central Medical Laboratory Limited Partnership
GDML Medical Laboratories Inc
Health Trans Services Inc.
HHLA Lab-In-An-Envelope, LLC
Home Healthcare Laboratory of America, LLC
IDX Pathology, Inc.
Impact Genetics Corp
Impact Genetics, Inc.
Kaleida LabCorp, LLC
Lab Delivery Service of New York City, Inc.
LabCorp Belgium Holdings, Inc.
LabCorp BVBA
LabCorp Central Laboratories (Canada) Inc.
LabCorp Central Laboratories (China) Inc.
LabCorp Central Laboratories (Singapore) Pte.
LabCorp Development Company
LabCorp Employer Services, Inc.
LabCorp Health System Diagnostics, LLC
LabCorp Indiana, Inc.
LabCorp Japan, G.K.
LabCorp Limited
LabCorp Michigan, Inc.
LabCorp Nebraska, Inc.
LabCorp Neon Ltd.
LabCorp Neon Switzerland S.à.r.l.
LabCorp Specialty Testing Billing Service, Inc.
LabCorp Specialty Testing Group, Inc.
LabCorp Staffing Solutions, Inc.
LabCorp Tennessee, LLC
LabCorp UK Holdings, Ltd.
Laboratoire Bio-Medic Inc.
Laboratory Corporation of America
LabWest, Inc.
Lifecodes Corporation
LipoScience, Inc.
Litholink Corporation
Medical Neurogenitics, LLC
Medtox Diagnostics, Inc.
Medtox Laboratories, Inc.
MEDTOX Scientific, Inc.
Monogram Biosciences UK Limited
Monogram Biosciences, Inc.
National Genetics Institute
New Brighton Business Center LLC
New Imaging Diagnostics, LLC
New Molecular Diagnostics Ventures LLC
NWT Inc.
Orchid Cellmark Ltd.
Orchid Cellmark ULC
PA Labs, Inc.
Path Lab Incorporated
Pathology Associates Medical Lab, LLC
Pee Dee Pathology Associates, Inc.
Persys Technology Inc.
Pixel by LabCorp
Princeton Diagnostic Laboratories of America, Inc.
Protedyne Corporation
ReliaGene Technologies Inc.
Saint Josephs-PAML, LLC
Sequenom Biosciences (India) Pvt. Ltd.
Sequenom Center for Molecular Medicine, LLC
Sequenom, Inc.
Southern Idaho Regional Laboratory
SW/DL LLC
Tandem Labs Inc.
The LabCorp Charitable Foundation
Tri-Cities Laboratory, LLC
Viro-Med Laboratories, Inc.
Yakima Medical Arts, Inc.
Covance Inc. Active Entities
CJB Inc.
Covance (Argentina) S.A.
Covance (Asia) Pte. Ltd.
Covance (Barbados) Holdings Ltd.
Covance (Barbados) Ltd.
Covance (Canada) Inc.
Covance (Polska) Sp.Zo.O
Covance Asia-Pacific Inc.
Covance Austria GmbH
Covance Bioanalytical Services LLC
Covance Brazil Pharmaceutical Services Limitada
Covance Central Laboratory Services Inc.
Covance Central Laboratory Services Limited Partnership
Covance Central Laboratory Services S.a r.l.
Covance Chile Services Limitada
Covance Clinical and Periapproval Services AG
Covance Clinical and Periapproval Services SRL
Covance Clinical and Periapproval Services Limited
Covance Clinical and Periapproval Services LLC
Covance Clinical Development GmbH
Covance Clinical Development Private Limited
Covance Clinical Development S.A.
Covance Clinical Development S.R.L.
Covance Clinical Development SRL
Covance Clinical Development SARL
Covance Clinical Product Developments Ltd.
Covance Clinical Research Unit Inc.
Covance Clinical Research Unit Limited
Covance Clinical Research, L.P.
Covance CLS Holdings Limited LLC
Covance CLS Holdings Partnership LP
Covance Colombia Services Limitada
Covance Consulting Limited
Covance CRS Analytics Ltd.
Covance CRS Developments Limited
Covance CRS International Limited
Covance CRS Limited
Covance CRU Inc.
Covance Denmark Aps
Covance Development Services (Pty) Ltd
Covance Guatemala Services, S.A.
Covance Hong Kong Holdings Limited
Covance Hong Kong Services Limited
Covance Hungaria Consultancy Limited Liability Company
Covance India Pharmaceutical Services Private Limited
Covance International Holdings B.V.
Covance Japan Co., Ltd.
Covance Korea Services Limited
Covance Laboratories Inc.
Covance Laboratories Limited
Covance Latin America Inc.
Covance Limited
Covance Luxembourg S.a r.l.
Covance Market Access Services Inc.
Covance Mexico Services, S. DE R. L. De C.V.
Covance Neon Luxembourg S.a r.l.
Covance New Zealand Limited
Covance Periapproval Services Inc.
Covance Peru Services S.A.
Covance Pharma Consulting Limited
Covance Pharmaceutical Research and Development (Beijing) Co., Ltd.
Covance Pharmaceutical Research and Development (Shanghai) Co., Ltd.
Covance Preclinical Corporation
Covance Preclinical Services GmbH
Covance Pty Ltd
Covance Research Holdings, LLC
Covance Scientific Services & Solutions Private Limited
Covance Scientific Services & Solutions, Inc.
Covance Services (Thailand) Limited
Covance Services Malaysia Sdn. Bhd.
Covance Specialty Pharmacy LLC
Covance Taiwan Services Limited
Covance US Holdings Limited LLC
Covance US Holdings Partnership LP
Covance Virtual Central Laboratory B.V.
Fairfax Storage Limited
Global Specimen Solutions, Inc.
Hazpen Trustees Ltd.
LSR Pension Scheme Limited
Medaxial Limited
Sciformix Europe Limited
SnapIot, Inc.
SnapIot Europe SRL
Texas Covance GP, Inc.
Covance Inc. Inactive Entities
Covance Classic Laboratory Services Inc.
Covance Genomics Laboratory LLC
Covance Laboratories Korea Company Limited
Covance NPA Inc.
Integrated Safe Foods Limited
International Food Network Ltd
JSG R&D LLC
Nexigent Inc.
PMD Properties, LLC
REIM LLC
Safe Foods International Holdings LLC
SLJK LLC
SPHN LLC
Chiltern International Group Limited Operating Entities
Chiltern - Pesquisa Clinica Ltda
Covance Clinical Research Ukraine LLC
Chiltern International Group Ltd. (CIGL) HL
Chiltern International Holdings Limited
Chiltern Investigacion Clinica Ltda
Chiltern Clinical Research Ukraine LLC
Endpoint Clinical (UK) Ltd.
Endpoint Clinical, Inc.
Endpoint Clinical India Private Limited
Havenfern Limited
Ockham Development Group (Holdings) UK Limited
Ockham Europe Ltd.
Theorem Clinical Research Holdings B.V.
Theorem Clinical Research International B.V.
Theorem Clinical Research Latin America B.V.
Theorem Clinical Research Pte. Ltd.
Theorem Research Associates, Inc.
Chiltern International Inactive Entities
Chiltern Clinical Research (Philippines) Inc.
Chiltern International AB
Chiltern International Limited
Chiltern International Ltd
Chiltern Pharmaceutical and Technology Consulting (Shanghai) Co. Ltd.
Integrated Development Associates Philippines, Inc.
Theorem Clinical Research Co., Ltd.
Dynacare non-operating entities identified subsequent to the acquisition of Dynacare Inc. on July 25, 2002
1004679 Ontario Limited
563911 Ontario Limited
794475 Ontario Inc.
829318 Ontario Limited
854512 Ontario Limited
879606 Ontario Limited
900747 Ontario Ltd.
925893 Ontario Limited
942487 Ontario Ltd.
942489 Ontario Ltd.
942491 Ontario Limited
942492 Ontario Ltd.
947342 Ontario Ltd.
949235 Ontario Ltd.
958069 Ontario Inc.
977681 Ontario Inc.
978550 Ontario Ltd.
978551 Ontario Ltd.
Amherstview Medical Centre Developments Inc.
DHG Place Du Centre Clinique
Dynacare Canada Inc.
Dynacare International Inc.
Glen Davis Equities Ltd.
L.R.C. Management Service Inc.
Lawrence-Curlew Medical Centre Inc.
Roselat Developments Limited
St. Joseph's Health Centre
Stockwin Corporation Ltd.
Thistle Place Care Corp.
Toronto Argyro Medical Laboratories Ltd.
Woodstock Medical Arts Building Inc.
Exhibit 23.1
CONSENT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
We hereby consent to the incorporation by reference in the Registration Statements on Form S-3 (No. 333-234633) and Form
S-8 (No. 333-150704, No. 333-181107, No. 333-211324 and No. 333-211323) of Laboratory Corporation of America
Holdings of our report dated February 25, 2021, relating to the financial statements and the effectiveness of internal control
over financial reporting, which appears in this Form 10-K.
/s/ PricewaterhouseCoopers LLP
Raleigh, North Carolina
February 25, 2021
Exhibit 24.1
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart her true and lawful attorney-in-fact and agent, with full power of substitution, for her and in her name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as she might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or she substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ KERRII B. ANDERSON
Kerrii B. Anderson
Exhibit 24.2
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart his true and lawful attorney-in-fact and agent, with full power of substitution, for him and in his name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as he might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or his substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ JEAN-LUC BÉLINGARD
Jean-Luc Bélingard
Exhibit 24.3
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart his true and lawful attorney-in-fact and agent, with full power of substitution, for him and in his name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as he might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or his substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ JEFFREY A. DAVIS
Jeffrey A. Davis
Exhibit 24.4
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart his true and lawful attorney-in-fact and agent, with full power of substitution, for him and in his name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as he might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or his substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ D. GARY GILLILAND, M.D., Ph.D
D. Gary Gilliland, M.D., Ph.D
Exhibit 24.5
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart his true and lawful attorney-in-fact and agent, with full power of substitution, for him and in his name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as he might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or his substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ GARHENG KONG, M.D., Ph.D.
Garheng Kong, M.D., Ph.D.
Exhibit 24.6
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart his true and lawful attorney-in-fact and agent, with full power of substitution, for him and in his name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as he might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or his substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ PETER M. NEUPERT
Peter M. Neupert
Exhibit 24.7
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart her true and lawful attorney-in-fact and agent, with full power of substitution, for her and in her name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as she might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or her substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ RICHELLE P. PARHAM
Richelle P. Parham
Exhibit 24.8
POWER OF ATTORNEY
KNOWN ALL MEN BY THESE PRESENTS, that the undersigned hereby constitutes and appoints Sandra van
der Vaart his true and lawful attorney-in-fact and agent, with full power of substitution, for him and in his name,
place and stead, in any and all capacities, in connection with the Laboratory Corporation of America Holdings
(Corporation) Annual Report on Form 10-K for the year ended December 31, 2020, under the Securities Exchange
Act of 1934, as amended, including, without limiting the generality of the foregoing, to sign the Form 10-K in the
name and on behalf of the Corporation or on behalf of the undersigned as a director or officer of the Corporation,
and any amendments to the Form 10-K and any instrument, contract, document or other writing, of or in connection
with the Form 10-K or amendments thereto, and to file the same, with all exhibits thereto, and other documents in
connection therewith, including this power of attorney, with the Securities and Exchange Commission and any
applicable securities exchange or securities self-regulatory body, granting unto said attorneys-in-fact and agents,
each acting alone, full power and authority to do and perform each and every act and thing requisite and necessary to
be done in and about the premises, as fully to all intents and purposes as he might or could do in person, hereby
ratifying and confirming all that said attorney-in-fact and agents, each acting alone, or his substitute or substitutes,
may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, the undersigned has signed these presents in this 25th day of February, 2021.
By:
/s/ R. SANDERS WILLIAMS, M.D.
R. Sanders Williams, M.D.
Exhibit 31.1
Certification
I, Adam H. Schechter, certify that:
1. I have reviewed this Annual Report on Form 10-K of Laboratory Corporation of America Holdings;
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact
necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading
with respect to the period covered by this report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all
material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods
presented in this report;
4. The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and
procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined
in Exchange Act Rule 13a-15(f) and 15d-15(f)) for the registrant and have:
a) designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed
under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries,
is made known to us by others within those entities, particularly during the period in which this report is being prepared;
b) designed such internal control over financial reporting, or caused such internal control over financial reporting to be
designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the
preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
c) evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our
conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this
report based on such evaluation; and
d) disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the
registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has
materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over
financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons
performing the equivalent functions):
a) all significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting
which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial
information; and
b) any fraud, whether or not material, that involves management or other employees who have a significant role in the
registrant’s internal control over financial reporting.
Date: February 25, 2021
By: /s/ ADAM H. SCHECHTER
Adam H. Schechter
Chief Executive Officer
(Principal Executive Officer)
Exhibit 31.2
Certification
I, Glenn A. Eisenberg, certify that:
1. I have reviewed this Annual Report on Form 10-K of Laboratory Corporation of America Holdings;
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact
necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading
with respect to the period covered by this report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all
material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods
presented in this report;
4. The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and
procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined
in Exchange Act Rule 13a-15(f) and 15d-15(f)) for the registrant and have:
a) designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed
under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries,
is made known to us by others within those entities, particularly during the period in which this report is being prepared;
b) designed such internal control over financial reporting, or caused such internal control over financial reporting to be
designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the
preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
c) evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our
conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this
report based on such evaluation; and
d) disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the
registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has
materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over
financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons
performing the equivalent functions):
a) all significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting
which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial
information; and
b) any fraud, whether or not material, that involves management or other employees who have a significant role in the
registrant’s internal control over financial reporting.
Date: February 25, 2021
By: /s/ GLENN A. EISENBERG
Glenn A. Eisenberg
Chief Financial Officer
(Principal Financial Officer)
Exhibit 32
Written Statement of
Chief Executive Officer and Chief Financial Officer
Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 (18 U.S.C. Section 1350)
The undersigned, the Chief Executive Officer and the Chief Financial Officer of Laboratory Corporation of America
Holdings (Company), each hereby certifies that, to his knowledge on the date hereof:
(a) the Form 10-K of the Company for the Period Ended December 31, 2020, filed on the date hereof with the
Securities and Exchange Commission (Report) fully complies with the requirements of Section 13(a) or 15(d) of the Securities
Exchange Act of 1934; and
(b) information contained in the Report fairly presents, in all material respects, the financial condition and results of
operations of the Company.
By:
By:
/s/ ADAM H. SCHECHTER
Adam H. Schechter
Chief Executive Officer
February 25, 2021
/s/ GLENN A. EISENBERG
Glenn A. Eisenberg
Chief Financial Officer
February 25, 2021
A signed original of this written statement required by Section 906, or other document authenticating, acknowledging, or
otherwise adopting the signature that appears in typed form within the electronic version of this written statement required by
Section 906, has been provided to Laboratory Corporation of America Holdings and will be retained by Laboratory Corporation
of America Holdings and furnished to the Securities and Exchange Commission or its staff upon request.