Omnicell Annual Report 2014

FY2014 Annual Report · Omnicell

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Table of Contents

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
____________________________________________________________________________

FORM 10-K

(Mark One)

 ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE

ACT OF 1934

For the fiscal year ended December 31, 2014

 TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE

ACT OF 1934

For the transition period from to

Commission File No. 000-33043

OMNICELL, INC.

(Exact name of Registrant as specified in its charter)

Delaware
(State or other jurisdiction of
incorporation or organization)

94-3166458
(IRS Employer
Identification No.)

590 East Middlefield Road
Mountain View, CA 94043
(Address of registrant's principal executive offices, including zip code)

(650) 251-6100
(Registrant's telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Common Stock, $0.001 par value

Name of each exchange on which registered

The NASDAQ Stock Market LLC

Securities registered pursuant to Section 12(g) of the Act: None

Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes  No 

Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act. Yes  No 

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  No 

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Website, if any, every Interactive Data File
required to be submitted and posted 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 and post such files). Yes  No 

Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not be contained, to

the best of registrant's knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to
this Form 10-K. 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company.

See the definitions of "large accelerated filer," "accelerated filer" and "smaller reporting company" in Rule 12b-2 of the Exchange Act. (Check one):

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Large accelerated filer 

Accelerated filer 

Non-accelerated filer 
(Do not check if a
smaller reporting company)

Smaller reporting company 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes  No 

The aggregate market value of the registrant's common stock, $0.001 par value, held by non-affiliates of the registrant as of June 30, 2014 was $1.0

billion (based upon the closing sales price of such stock as reported on The NASDAQ Global Select Market on such date) which excludes an aggregate of
1,214,401 shares of the registrant's common stock held by officers, directors and affiliated stockholders. For purposes of determining whether a stockholder
was an affiliate of the registrant at June 30, 2014, the registrant has assumed that a stockholder was an affiliate of the registrant at June 30, 2014 if such
stockholder (i) beneficially owned 10% or more of the registrant's common stock and/or (ii) was affiliated with an executive officer or director of the registrant
at June 30, 2014. Exclusion of such shares should not be construed to indicate that any such person possesses the power, direct or indirect, to direct or cause the
direction of the management or policies of the registrant or that such person is controlled by or under common control with the registrant.

As of February 20, 2015 there were 36,166,305 shares of the registrant's common stock, $0.001 par value, outstanding.

DOCUMENTS INCORPORATED BY REFERENCE

Portions of the registrant's definitive Proxy Statement for the 2015 Annual Meeting of Stockholders to be filed with the Securities and Exchange
Commission pursuant to Regulation 14A not later than 120 days after the end of the fiscal year covered by this Form 10-K are incorporated by reference in
Part III, Items 10-14 of this Form 10-K.

Table of Contents

PART I
Item 1.

Item 1A.

Item 1B.

Item 2.

Item 3.

Item 4.

PART II
Item 5.

Item 6.

Item 7.

OMNICELL, INC.

2014 Form 10-K Annual Report

TABLE OF CONTENTS

Page No.

Business

Risk Factors

Unresolved Staff Comments

Properties

Legal Proceedings

Mine Safety Disclosures

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

Item 7A.

Quantitative and Qualitative Disclosures About Market Risk

Item 8.

Item 9.

Item 9A.

Item 9B.

PART III
Item 10.

Item 11.

Item 12.

Item 13.

Item 14.

PART IV
Item 15.

Signatures

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

Executive Compensation

Security Ownership of Certain Beneficial Owners and Management and Related
Stockholder Matters
Certain Relationships, Related Transactions and Director Independence

Principal Accountant Fees and Services

Exhibits and Financial Statement Schedules

Reports of Independent Registered Public Accounting Firms

OTHER

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FORWARD-LOOKING STATEMENTS AND FACTORS THAT MAY AFFECT FUTURE RESULTS

This annual report on Form 10-K contains forward-looking statements. The forward-looking statements are contained

principally in the sections entitled “Risk Factors” and “Management's Discussion and Analysis of Financial Condition and
Results of Operations.” These statements involve known and unknown risks, uncertainties and other factors which may cause
our actual results, performance or achievements to be materially different from any future results, performances or
achievements expressed or implied by the forward-looking statements. Forward-looking statements include, but are not limited
to, statements about:

• our expectations regarding our future product bookings, which consist of all firm orders, as evidenced by a

•

contract and purchase order for equipment and software and, generally, by a purchase order for consumables.
Equipment and software bookings are installable within 12 months and consumables are generally recorded as
revenue within one month;
the extent and timing of future revenues, including the amounts of our current backlog, which represents firm
orders that have not completed installation and therefore have not been recognized as revenue;
•
the size or growth of our market or market share;
•
the opportunity presented by new products, emerging markets and international markets;
• our ability to align our cost structure and headcount with our current business expectations;
•
• our ability to protect our intellectual property and operate our business without infringing upon the intellectual

the operating margins or earnings per share goals we may set;

property rights of others;

• our ability to generate cash from operations and our estimates regarding the sufficiency of our cash resources;

and

• our ability to acquire companies, businesses, products or technologies on commercially reasonable terms and

integrate such acquisitions effectively.

In some cases, you can identify forward-looking statements by terms such as "anticipates," "believes," "could," "estimates,"

"expects," "intends," "may," "plans," "potential," "predicts," "projects," "should," "will," "would" and similar expressions intended to identify
forward-looking statements. Forward-looking statements reflect our current views with respect to future events, are based on
assumptions and are subject to risks and uncertainties. We discuss many of these risks in this annual report in greater detail in
Part II - Section 1A. “Risk Factors” below. Given these uncertainties, you should not place undue reliance on these forward-
looking statements. Also, forward-looking statements represent our estimates and assumptions only as of the date of this annual
report. You should also read this annual report and the documents that we reference in this annual report and have filed as
exhibits, completely and with the understanding that our actual future results may be materially different from what we
expect. All references in this report to "Omnicell," "our," "us," "we," or the "Company" collectively refer to Omnicell, Inc., a Delaware
corporation, and its subsidiaries. The term "Omnicell, Inc.," refers only to Omnicell, Inc., excluding its subsidiaries.

Except as required by law, we assume no obligation to update any forward-looking statements publicly, or to update

the reasons actual results could differ materially from those anticipated in any forward-looking statements, even if new
information becomes available in the future.

We own various trademarks, copyrights and trade names used in our business, including the following: Omnicell®, the

Omnicell logo, OmniRx®, OmniCenter®, OmniSupplier®, OmniBuyer®, SafetyStock®, WorkflowRx™, OmniLinkRx™,
SecureVault™, Optiflex™, SinglePointe™, AnywhereRN™, Anesthesia Workstation™ , Savvy™, MTS Medication
Technologies®, the MTS Medication Technologies logo, Medlocker®, AccuFlex®, Autobond ™, AutoGen ™, easyBLIST™,
Pandora®, OnDemand®, Multi-Med™, RxMap®, MTS-350 ™, MTS-400 ™, MTS-500 ™ and SureMed. This report also
includes other trademarks, service marks and trade names of other companies. All other trademarks used in this report are
trademarks of their respective holders.

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ITEM 1. BUSINESS

Overview

PART I

We are a leading provider of automation and business information solutions designed to enable healthcare systems to
streamline the medication administration process and manage costly medical supplies for increased operational efficiency and
enhanced patient safety.

More than 3,000 customers worldwide have utilized Omnicell Automation and Analytics solutions to help increase

operational efficiency, reduce errors, deliver actionable intelligence and improve patient safety. Omnicell Medication
Adherence solutions, including its MTS Medication Technologies brand, provide innovative medication adherence packaging
solutions designed to help reduce costly hospital readmissions. In addition, these solutions help enable approximately 6,000
institutional and retail pharmacies worldwide to maintain high accuracy and quality standards in medication dispensing and
administration while optimizing productivity and controlling costs.

The medical industry has become increasingly aware that human factors inevitably create the risk of medication

administration errors in the course of patient care.

The Institute of Medicine, a non-profit, non-governmental arm of the National Academies, published a report in 2006

that estimated that 1.5 million medication errors are made each year in the United States. Acute care facilities are required to
adhere to medication regulatory controls that we believe cannot be adequately supported by manual tracking systems or
partially automated systems. Any nursing shortages would add an additional challenge to acute care facilities to meet regulatory
controls and improve patient safety while still providing adequate patient care. Non-acute care facilities face similar safety
challenges. In its 2003 "Adherence to Long-Term Therapies-Evidence for Action," the World Health Organization stated,
“Across diseases, adherence is the single most important modifiable factor that compromises treatment outcome.” U.S. health
system thought leaders see medication adherence as a key requirement for closing the medication loop and delivering better
clinical outcomes and financial results. Medication non-adherence is described as a critical problem creating approximately
$290 billion in extra costs per year resulting in approximately 125,000 deaths per year, according to the New England
Healthcare Institute. In addition, the Centers for Medicare & Medicaid Services stated in 2012 that 11% of all hospital
admissions were related to medication non-adherence.

We provide solutions to help healthcare systems and caregivers address these aforementioned needs. We believe our
solutions align us with the long-term trends of the healthcare market to manage the health of patients across the continuum of
care, and that our patient-centric medication and supply management solutions help improve workflow efficiencies and patient
outcomes.

Operating Segments and Products

Our business is organized into two operating segments distinguished by products based on customer needs. In the first

quarter of 2014, we modified our segment reporting structure to match our new operating structure. The two operating
segments are Automation and Analytics and Medication Adherence.

Automation and Analytics

The Automation and Analytics segment is organized around the design, manufacturing, selling and servicing of

medication and supply dispensing systems, pharmacy inventory management systems, and related software. Our Automation
and Analytics products are designed to enable our customers to enhance and improve the effectiveness of the medication-use
process, the efficiency of the medical-surgical supply chain, overall patient care and clinical and financial outcomes of medical
facilities. Through modular configuration and upgrades, our systems can be tailored to specific customer needs.

Medication Adherence

The Medication Adherence segment primarily includes the manufacturing and selling of consumable medication

blister cards, packaging equipment and ancillary products and services. These products are used to manage medication

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administration outside of the hospital setting and include medication adherence products sold under the brand name MTS
Medication Technologies ("MTS"), Surgichem Limited ("Surgichem") and the Omnicell brand. MTS products consist of
proprietary medication packaging systems and related products for use by institutional pharmacies servicing long-term care,
and correctional facilities or retail pharmacies serving patients in their local communities. Similarly, Surgichem is a provider of
medication adherence packaging systems and solutions to the U.K. community and home care markets.

Financial Information by Segment

For information regarding our revenues, cost of revenues, gross profit and income from operations by segment, see
Note 17, Segment Information, of the Notes to Consolidated Financial Statements and Item 7, Management’s Discussion and
Analysis of Financial Condition and Results of Operations in this annual report.

Business Strategy

Our key business strategies include:

• Further penetrating existing markets through technological leadership by:

• Consistently innovating our product and service offerings; and

• Maintaining our customer-oriented product installation process.

•

Increasing penetration of new markets, such as non-acute care and international markets by:

• Launching new products and technologies that are specific to the needs of those markets;

• Building and establishing direct sales, distribution or other capabilities when and where it is appropriate;

• Partnering with companies that have sales, distribution or other capabilities that we do not possess; and

•

Increasing customer awareness of safety issues in the administration of medications;

• Expanding our product offering through acquisitions and partnerships.

Our solutions are designed to provide everything the customer requires for installation and maintenance of medication,

medical and surgical supply control. Our vision of improving healthcare for everyone has led us to take certain steps in the
development of our business and our long term approach to our market, such as:

• Providing a full service, positive experience for our hospital customers in the solution sales process, the timing

and implementation of our product installations and the responsiveness of our support services;

• Delivering solutions that are designed to provide our customers with the best experience in the healthcare

industry, as measured by customer input and third party surveys;

•

Innovating products to address patient safety and cost-containment pressures facing healthcare facilities while
improving clinician workflow and overall operating efficiency;

Incorporating a broad range of clinical input into our product solution development to accommodate needs
ranging from those of institutional pharmacies and stand-alone community hospitals to multi-hospital entities and
integrated delivery networks ("IDNs");

• Developing new solutions to enhance our customers' existing systems and protect our customers' investments by
preserving, leveraging and upgrading their existing information systems, as well as striving to provide integration
of our products with the other healthcare information systems used by our customers; and

• Providing flexibility in our systems that can be tailored to specific customer needs through modular upgrades,

thereby protecting our customers' investments.

We have developed or acquired numerous technologies that provide long-term solutions for our customers. Our own

product development activities have brought a number of innovative and proprietary products to the market. Our most recently

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announced solutions include the fourth generation Omnicell G4 platform with the Unity database across the automated
medication dispensing system. The Unity database is designed to decrease the risk of human error and save significant
pharmacy time by eliminating the need for repetitive entry of drug formularies in multiple locations. The Unity G4 platform is
designed to help our customers closely manage medication and supply inventory to reduce costs, comply with increasingly
stringent regulatory requirements and safeguard the patient.

In addition to our own development, we have acquired products that extend patient safety controls to a wider range of

applications and departments in the hospital. These include products for the central pharmacy, the operating room, the
catheterization lab, the nursing areas and the patient point of care. Our most recent acquisitions include MTS Medication
Technologies in 2012, which extended our product line to include solutions for Medication Adherence customers, and
Surgichem in 2014, which further extends our Medication Adherence solutions in Europe. Through continued internal
development and acquisitions, we intend to improve our current product offerings and expect to expand future product
offerings to enable healthcare facility clinicians to automate and control more of the medication, and medical and surgical
supply distribution processes, while providing an even greater ability to improve patient safety.

Industry Background

The delivery of healthcare in the United States still relies on a significant number of manual and paper-based

processes. Most hospitals have deployed at least some automation solutions, but few have deployed them throughout the
institution. The use of manual and paper-based systems in many hospital departments today results in highly complex and
inefficient processes for tracking and delivering medications and supplies. In addition, many existing healthcare information
systems are unable to support the modernization of healthcare delivery processes or address mandated patient safety initiatives.
These factors have contributed to medical errors and unnecessary process costs across the healthcare sector.

Healthcare providers and facilities are also affected by significant economic pressures. Rising costs of labor,

prescription drugs and new medical technology all contribute to increased spending. Governmental pressures surrounding
healthcare reform have led to increased scrutiny of the cost and efficiency with which healthcare providers deliver their
services. These factors, combined with the continuing consolidation in the healthcare industry, have significantly increased the
need to improve the efficiency of healthcare professionals and to control costs.

Our Automation and Analytics products are sold worldwide to a wide variety of healthcare institutions, but most of our

sales occur to acute care hospital customers in the United States. The United States acute care hospital market is comprised of
approximately 6,500 hospitals and other facilities with a total capacity of approximately 950,000 acute care beds. Our
customers include single location community hospitals, government hospitals and regional and national entities.

We also sell our Automation and Analytics products directly to non-acute care providers, which includes all healthcare

facilities that are not hospitals, and organizations that supply non-acute care providers. We estimate there are approximately
49,000 facilities in the United States that could utilize our Automation and Analytics products and very few of them are using
our solutions at this time.

Outside the United States, healthcare providers are becoming increasingly aware of the benefits of automation. Many
governmental and private entities look to the progress made over the last several years in the United States and are starting to
invest significantly in information technology and automation. BCC Research reports that worldwide inpatient pharmacy
automation revenue growth in our industry is expected to be 8.5% between 2013 and 2018. We sell our Automation and
Analytics products in a variety of countries, but to date we have focused our sales efforts on Canada, the United Kingdom, the
countries of the Middle East region, and China.

Our Medication Adherence products are also sold to a variety of healthcare providers, but most of our revenue in this

segment is from institutional and retail pharmacies. In the United States, where approximately 73% of our Medication
Adherence business occurs, the market is comprised of approximately 4,000 institutional pharmacies operated by 1,500
companies that service over 15,000 long-term care facilities. According to IMS Healthcare, Inc. ("IMS"), an independent third
party provider of information to the pharmaceutical and healthcare industry, pharmaceutical sales are expected to grow
approximately 1% to 4% annually through 2016. IMS expects that certain sectors of the market, such as biotechnology and
other specialty and generic pharmaceuticals, will grow faster than the overall market which suggests opportunities for the

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market in which we operate. In addition to medication control at long-term care facilities, our Multi-medication products
provide packaging that simplifies the process for individuals providing self-care to track and administer medications.

Key Industry Events and Reports

Reports by the Institute of Medicine, the Food and Drug Administration ("FDA"), and The Joint Commission have

increased awareness of the adverse impacts of medication errors. Regulatory standards and industry guidelines, such as those
published by the Institute for Safe Medication Practices, as well as the desire of healthcare organizations to improve quality and
avoid liability, have driven acute care facilities to prioritize investment in capital equipment, including automated medication
dispensing cabinets, which are a standard of care, to improve patient safety. Such reports and regulatory standards include the
following:

•

In 2012, The Joint Commission updated its medication management standards which include MM.03.01.01
requiring that medication storage is designed to assist in maintaining medication integrity, promote the availability
of medications when needed, minimize the risk of medication diversion, and reduce potential dispensing errors.

In 2010, the FDA updated its guidance that requires linear bar codes on most prescription drugs. Drug
manufacturers, re-packagers, re-labelers and private label distributors are subject to the rule. The FDA estimated
that the bar code rule, once implemented, would result in a 50% reduction in medication errors, 500,000 fewer
adverse drug events over the subsequent 20 years, $93 billion in cost savings and other economic benefits.

In 2002, The Joint Commission established the National Patient Safety Goals ("NPSG") program. In 2010, NPSG
03.04.01, National Patient Safety Goal on Labeling Medications, required the labeling of all medications,
medication containers (syringes, medicine cups, basins, etc.) and other solutions on and off the sterile field in
perioperative and other procedural settings.

Leading academic medical centers are among those customers benefiting from our technologies, and our customers

include 10 of the 18 U.S. News & World Report Honor Roll of Best Hospitals 2013-2014.

Medication errors can occur in post-acute settings as well. Medication non-adherence is extremely common.
According to research by Osterberg and Blaschke published in the New England Journal of Medicine in 2005, more than half
of the 3.2 billion prescriptions dispensed annually in the United States are not taken as prescribed, and according to numerous
studies, the same non-adherence rate exists for chronic disease medications. Poor adherence results in significant morbidity,
mortality and avoidable healthcare costs. The New England Healthcare Institute estimated in 2009 that medication non-
adherence was the major driver of $290 billion per year in avoidable healthcare costs, equivalent to 13% of total national health
expenditures.

Medication adherence can be improved through attitudinal and behavioral changes, which pharmacists can encourage

and help facilitate by providing interventional support, including adherence tools, such as blister cards, which are commonly
used in post-acute settings. A 2011 study by CVS Caremark published in Health Affairs concluded that the medical cost per
patient with chronic vascular disease was $13,000 to $39,000, annually, and patients who take medications as directed by
physicians experienced medical savings ranging from $1,900 to $8,900, annually. The study also found that these patients
experienced fewer emergency room visits and inpatient hospital stays.

Healthcare Reform

In 2009, the U.S. government passed the American Reinvestment and Recovery Act ("ARRA") which provides for,

among other things, the funding of incentives for healthcare organizations to implement Electronic Healthcare Records
("EHR"). ARRA establishes minimal requirements for electronic healthcare record usage and provides incentives for electronic
healthcare record adoption through 2015 and penalties for non-adoption after 2015. In 2010, the U.S. Congress passed the
Patient Protection and Affordable Care Act ("PPACA"), which prescribes broad-based measures designed to provide healthcare
to a greater percentage of the population. We believe that both the ARRA and the PPACA will drive the need for increased
efficiency in providing healthcare without reducing healthcare standards.

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We believe our products assist healthcare organizations in achieving the goals of the new laws by allowing them to
reduce process steps, eliminate manual tracking and waste, enable population-level performance insights, track quality levels
and reduce errors that result in unnecessary cost. Our Unity G4 platform includes an automated dispensing system that is
Modular EHR stage 2 certified and works with all "hospital information system vendors," as defined by the U.S. Department of
Health and Human Services Office of National Coordinator for Health Information Technology. Our Pandora Healthcare Data
Analytics solution provides enterprise-level insights that can assist in monitoring hospital performance and quality of care. Our
Unity platform solutions help decrease the risk of human error and save significant pharmacy time by eliminating the need for
repetitive entry of drug formularies in multiple locations. Our Unity platform is designed to help hospitals closely manage
medication and supply inventory to reduce costs, comply with increasingly stringent regulatory pressures and safeguard the
patient.

Automation and Analytics Products and Services

Our Automation and Analytics products are designed to enable our customers to enhance and improve the

effectiveness of the medication-use process, the efficiency of the medical-surgical supply chain, overall patient care and clinical
and financial outcomes of medical facilities. Through modular configuration and upgrades, our systems can be tailored to
specific customer needs. From the point at which a medication arrives at the hospital receiving dock until the time it is
administered to the patient, our systems are capable of storing, packaging, bar coding, ordering and issuing the medication, as
well as providing information and controls on its use and reorder. Our medication-use product line includes systems for
medication dispensing in acute care nursing departments, central pharmacy automation, physician order management and
nursing workflow automation at the bedside. Our supply product lines provide healthcare facilities with cost data that enables
detailed quantification of charges for payer reimbursement, inventory management, implant monitoring and the timely
reordering of supplies. These products range from industrial-grade software-driven carousels for managing large amounts of
inventory in the central pharmacy to high-security closed-cabinet systems and software to open-shelf and combination solutions
in the nursing unit, catheterization lab and operating room. We also provide services, including customer education and
training, to help customers to optimize their use of our technology.

Our analytics solution allows pharmacists and materials managers to more easily manage inventory flow, tracking and

optimization, and aids in the identification of those engaged in narcotics diversion within the acute care facility.

Medication-Use Products

Our medication-use product line includes our OmniRx, SinglePointe, AnywhereRN, Pandora Data Analytics, Savvy

Mobile Medication System, OmniLinkRx, WorkflowRx, Central Pharmacy and Satellite Pharmacy Manager, Controlled
Substance Management and Anesthesia Workstation products. To provide our customers with end-to-end medication control,
our product line incorporates bar code technology throughout. Our solutions incorporate advanced software technology, which
we believe is the most advanced on the market today, and our G4 platform integrates disparate systems onto a single database.
Each of the products in our medication-use solution suite is summarized in the table below.

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Product

OmniRx

SinglePointe

AnywhereRN

Pandora Analytics

Savvy Mobile System

Use in Hospital

Any nursing area in a
hospital department that
administers medications

Description

Secure dispensing system that automates the
management and dispensing of medications at the point
of use
Software product for use in conjunction with the
OmniRx product that controls medications on a patient-
specific basis, allowing automated control of up to
100% of the medications used in a hospital

Any nursing area in a
hospital department that
administers medications

Software that allows nurses to remotely operate
automated dispensing cabinets from virtually any
workstation in the hospital

Hospital central pharmacy
and general hospital
management

Any nursing area in a
hospital department that
administers medications

OmniLinkRx

Hospital central pharmacy

WorkflowRx

Hospital central pharmacy

Central Pharmacy and Satellite
Pharmacy Manager
Controlled Substance Management

Hospital central pharmacy

Anesthesia Workstation

Operating room

Nursing Floor Solutions

Advanced reporting and data analytics tools

Mobile wireless computer and dispensing system that
provides a platform for hospital information systems and
a convenient and secure method for nurses to move
medication and supplies

Prescription routing system that allows nurses and
doctors to scan handwritten prescription orders for
electronic delivery to pharmacists for approval and
filling

Automated pharmacy storage, retrieval and packaging
systems
Software for managing inventory in central and satellite
pharmacy locations
Controlled substance inventory management system
Secure dispensing system for the management of
anesthesia supplies and medications

The OmniRx solution is the core of our medication control solutions. The OmniRx solution is a dispensing cabinet

that automates the management and dispensing of medications at the point of use. The OmniRx features biometric fingerprint
identification, advanced single-dose dispensing, bar code confirmation, integrated medication label printing and a wide range
of drawer modules enabling the establishment of various security levels. Software features of the OmniRx include patient
profiling, notification of medications due, a variety of security features, waste management, clinical pharmacology and
integration with an Internet browser for clinical reference information. OmniRx has met meaningful use criteria by obtaining
modular EHR certification, as defined by the Office of the National Coordinator. OmniRx is highly configurable to allow the
pharmacist the capability to tailor the usage of the system to specific regulatory controls and workflows.

The SinglePointe solution is a software extension to the OmniRx solution that allows pharmacists to automate the

distribution of patient-specific medications, enabling control of up to 100% of all medications through the automated
dispensing system. Controlling patient-specific medications through the OmniRx extends the benefits of automated medication
distribution, including increased patient safety, consistency in tracking and inventory control, simplification of procedures and
improved monitoring of controlled substances to a broader range of the medication distribution process in the hospital.

The AnywhereRN solution is a software solution that allows nurses to operate the automated dispensing cabinets

from virtually any remote workstation within the hospital. This software enables enhanced workflow for nurses such that they
are no longer limited to being directly in front of the cabinet to perform certain medication administration functions.
AnywhereRN is intended to reduce nurse distractions in the medication administration process, allowing cabinet operations to
be done in private or quieter areas. AnywhereRN is also intended to eliminate congestion at the cabinet by minimizing nurse
queuing to withdraw medications.

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The Pandora Analytics solution is comprised of reports and analytical software for medication diversion detection,
customizable user options, hospital inventory management controls, point-of-care data analytics and financial optimization.
Pandora Analytics is designed to assist hospitals in their efforts to improve patient safety, regulatory compliance and reduce
costs.

The Savvy Mobile Medication solution provides a mobile workstation for nurses, equipped with locking drawers for
secure transportation of medications and patient supply items. Savvy allows both tracking and physical control of medications
to be extended to the patient bedside. The Savvy Mobile Medication solution is designed to provide efficient workflow support,
allowing nurses to remotely access the automated dispensing cabinet using AnywhereRN, saving nursing time and minimizing
the risk of interruptions to enhance patient safety. This same mobile solution can be used to access hospital applications,
including electronic medical records and electronic medication administration records.

Central Pharmacy Solutions

The OmniLinkRx solution is a physician order software product that automates communication between nurses and
the pharmacy. Used in the central pharmacy, the OmniLinkRx solution simplifies the communication of handwritten physician
orders from remote nursing stations to the pharmacy.

The WorkflowRx solution is an automated storage, retrieval, inventory management and repackaging solution for the

central pharmacy. It is designed to help pharmacists ensure that the right medications are stored in and retrieved from proper
locations, both in the central pharmacy and in automated dispensing cabinets. The WorkflowRx solution is deployed on a
storage and retrieval carousel, on a repackaging system, or on both. The system may also be deployed only using bar code
scanners for hospitals that do not use carousels or packagers. Bar code administration through the WorkflowRx solution is
designed to help ensure that medications are stocked correctly from their point of entry into the healthcare facility. Labeling
medications with bar codes using a repackaging system enables bedside medication administration solutions, such as the Savvy
solution, to perform bar code checking at the patient bedside.

Central Pharmacy Manager and Satellite Pharmacy Manager are integrated software systems that automate

management of pharmacy inventory. Central Pharmacy Manager automates inventory management in the central pharmacy,
helping to reduce inventory costs and save staff time on ordering and receiving processes. Satellite Pharmacy Manager gives
pharmacists managing satellite locations visibility into inventory levels and costs at the remote sites within their health system.

The Controlled Substance Management solution provides perpetual inventory management and an automated audit
trail to help the pharmacy comply with regulatory standards for controlled substances while increasing efficiency. The shared
database between the pharmacy, the operating room and nursing cabinets tracks and monitors controlled substance movement
throughout the hospital, providing a true closed-loop solution. The Controlled Substance Management software, coupled with
our automated dispensing technology, enables healthcare facilities to track, monitor and control the movement of controlled
substances from the point of initial receipt from the wholesaler throughout internal distribution. The Controlled Substance
Management solution maintains a perpetual item inventory and complete audit using integrated bar code technology with both
fixed and portable scanners. Bar coded forms and labels may also be generated directly from the Controlled Substance
Management system.

Operating Room Solutions

The Anesthesia Workstation solution is a system for the management of anesthesia supplies and medications. The

system is tailored for the workflow of the clinician working in the operating room. The Anesthesia TT solution is a
fixed-position tabletop unit designed as a medication-only system. The Anesthesia Workstation incorporates ergonomics to
enhance the particular workflows inherent to the operating room and unique software to better handle case management in the
procedural areas.

Medical and Surgical Supply Products

Our medical and surgical supply products provide acute care hospitals control over consumable supplies critical to

providing quality healthcare. These solutions provide inventory control software that is designed to ensure that critical supplies

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are always stocked in the right locations. At the same time, usage tracking helps hospital administrators to ensure that money is
not wasted on excessive stores of supplies and helps optimize reimbursement by improving charge capture.

Implantable tissue and bone grafts can also be monitored and tracked for additional patient safety and regulatory

compliance. The bone and tissue features are integrated with our overall medical and surgical supply chain inventory
management and charge capture systems. These solutions are designed for use in the materials management department, the
nursing unit and specialty areas such as the catheterization lab and the operating room. They integrate with other information
management systems and use bar code technology extensively.

Our supply product line includes the Omnicell Supply Cabinet, Omnicell Open Supply Solution, Supply/Rx
Combination Cabinet, Omnicell Tissue Center, OptiFlex MS, OptiFlex SS, OptiFlex CL. Each of these products is summarized
in the table below.

Product

Use in Hospital

Description

Omnicell Supply Solution

Any nursing area in a hospital
department that uses patient care
supplies

Secure dispensing system that automates the
management and dispensing of medical and
surgical supplies at the point of use

Omnicell Open Supply Solution

Supply/Rx Combination Solution

Areas that require the management
of high volume/low dollar
inventory as well as areas where
space restrictions limit the ability
to install closed cabinets and other
areas such as off-site clinics

Ability to expand inventory management
capabilities by providing efficient workflow and
flexibility to enable either remote inventory
management from closed supply cabinets or
completely open shelf inventory management
from a touchscreen PC and Scanner

Any nursing area in a hospital
department that uses patient care
supplies and administers
medications

Secure dispensing system that manages both
supplies and medications from the same cabinets,
using the same user interface screens, in medical
and surgical units and specialty areas

Omnicell Tissue Center

Perioperative areas of the hospital

OptiFlex MS

Any nursing area in a hospital
department that administers
supplies

Manages the chain of custody for bone and tissue
specimens from the donor to the patient in the
operating room

System for the management of medical and
surgical supplies that provides the flexibility of
using bar code control in an open shelf
environment

OptiFlex SS

Perioperative areas of the hospital

Specialty modules for the perioperative areas

OptiFlex CL

Procedure areas in the hospital
including the cardiac
catheterization lab

Specialty modules for the cardiac catheterization
lab and other procedure areas

The Omnicell Supply Solution is a secure dispensing system that dispenses and tracks medical and surgical supplies
at the point of use. Specialty modules are available for a variety of solutions to manage implants and medications used across
the hospital as described below.

The Omnicell Open Supply Solution provides an efficient workflow solution that allows for expanded inventory

management from a closed supply cabinet or completely open shelf solution from a touchscreen PC and scanner.

Supply/Rx Combination Solution is designed to manage medications and supplies in one versatile cabinet or group

of cabinets. This solution allows each department to manage supplies and medications independently, while tracking
transaction data, inventory, expenses and treatment costs through a single system.

Omnicell Tissue Center allows the operating room staff to manage the chain of custody for bone and tissue
specimens from the donor to the patient in the operating room. This solution enables compliance with The Joint Commission
requirements and Association of Operating Room Nurses guidelines regarding the handling of tissue specimens.

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OptiFlex MS solution provides control over general medical and surgical supplies stored in open shelves or in

automated dispensing cabinets.

OptiFlex SS manages supplies and preference cards in the perioperative areas whether the supplies are stored on open
shelves or in automated dispensing cabinets. The preference-list system creates a unique bar code for each surgical case, based
on physician, procedure and patient and provides information on the case for data analysis, reporting and charge capture. The
Suture Module is designed to be integrated into the Omnicell Supply Solution to secure, dispense and automatically track
suture usage.

OptiFlex CL manages supplies and creates cases in the cardiac catheterization lab, interventional radiology suite and

other procedure areas. This solution allows real-time point-of-use data collection and accurate supply tracking regardless of
whether supplies are stored on open shelves or in automated dispensing cabinets. It also improves cost management through
automated charge capture and case profiling by the physician. The Catheter Module is designed to be integrated into the
Omnicell supply cabinet and allows hospitals to secure, dispense and electronically track accurate catheter usage. The Implant
Tracking Module records expiration date, lot and serial number information to help enable compliance with Joint Commission
and FDA requirements regarding surgical implants in the event of a recall.

Other Automation and Analytics Products and Services

Omnicell Interface Software provides interface and integration between our medication-use products or our supply

products and a healthcare facility's in-house information management systems. Interface software is designed to provide
integration and communication of patient data, logistical data, inventory information, charge capture and billing information
and other healthcare database information.

Services include customer education and training and maintenance and support services, provided on a time-and-
material basis. We also provide fixed period service contracts to our customers for post-installation technical support with
phone support, on-site service, parts and access to software upgrades. On-site service is provided by our field service team.

Medication Adherence Products and Services

We offer solutions to assist institutional and retail pharmacies in packaging medication for patient use in care

environments where there is a caregiver present and for environments where the patient is caring for themselves.

For environments where a caregiver is present, institutional and retail pharmacies use our solutions for packaging

medications into adherence packages that contain a 7- to 90-day supply of a specific single medication. The blister cards may
be pre-packaged ahead of time and placed into inventory until needed to fill a specific patient order, or on-demand, where
individual patient medication orders are packaged and labeled by an automated robotic system. Our solutions range from
manual sealers to fully automated packaging machines, the software that runs these machines, and the consumable packages
used in these machines. We have packaging solutions for any size pharmacy operation which are designed to increase pharmacy
output and improve dispensing accuracy, enabling improved patient safety and economics.

For environments where a patient cares for themselves, institutional and retail pharmacies use our solutions for

packaging medications into adherence packages that contain all the medications a single patient is prescribed into one seven-
day package. These products are primarily used in community-based pharmacies to assist in organizing complex medication
regimes into a simple to use solution that enhances medication adherence. Multi-medication packages are arranged so that all
the medications for a single dosing period are contained in one blister, eliminating confusion for the patient and providing the
caregivers increased assurance that medications are taken in the right sequence. Our solutions include automated packaging
machines that package specific patients medications on-demand, the software that runs these machines and the consumable
packages used in these machines.

In addition to packaging solutions, we sell specially configured versions of our OmniRx medication dispensing
machines to institutional pharmacies, which they place in long-term care facilities to manage narcotics and medications needed
quickly.

Single Medication Products For Use Where A Caregiver Is Present

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Pharmacy Sealers for Medication Packaging

Our heat-sealed blister cards require a sealer to create an impermeable barrier. By using specially designed equipment
to control heat, time and pressure, the institutional pharmacy serving the long-term care patients is able to create a quality seal
on every package, providing a secure barrier to moisture and gases. Within this range of equipment is a sealing solution suited
for almost any pharmacy, from a low volume manual blister card sealer to a high volume, all electric heat sealer with
programmable computer logic.

• The SureSeal is a programmable, manual sealer using heat and pressure. It is designed as a cost effective, entry

level sealer for low volume sealing of medication blister cards.

• The Autobond is a programmable, semi-automated heat and pressure sealer operating off of electricity and

compressed air. Autobond provides temperature and time controls for a consistent quality sealing.

• The AutoGen is a programmable, semi-automated heat and pressure sealer operating off of electricity only.

• The Gemini is a compact all-electric heat and pressure sealer.

Automated Fillers

Our semi-automated filling equipment is designed specifically for the long-term care institutional pharmacy with

enough order volume to warrant pre-packaging frequently-used medications into blister packs to keep in inventory awaiting a
patient order. This packaging equipment elevates pre-packaging to a higher level of efficiency, resulting in higher accuracy and
increased production levels. The systems combine both automated filling and sealing capabilities into one machine.

• The MTS-350 is a tabletop machine capable of filling a wide range of medications and features an ergonomic

design and easy-to-use controls. The MTS-350 provides a semi-automated mechanism for filling blister cards and
a sealer using compressed air and heat.

• The MTS-400 is ergonomically designed for high pre-pack volume for the medium to large pharmacy. The MTS-
400 provides a portable workstation with built-in compressor and storage so as not to take up valuable counter
space. Fully configured, the MTS-400 allows a single operator to perform the functions of filling, inspection,
sealing and labeling simultaneously.

• The MTS-500 is designed to automate pre-packaging in the pharmacy and is capable of producing up to 960 pre-
packaged blister cards per hour. It includes an integrated label applicator and conveyor to optimize output.

Pharmacy Automation Systems

Our OnDemand automated solutions are designed to meet the broad needs of pharmacies to package individual patient

medication orders accurately and efficiently. These machines interface with pharmacy information systems to obtain patient-
specific prescription information which enables on-demand packaging capabilities for our larger institutional pharmacy
customers. Our current line of OnDemand machines includes the following products:

• AccuFlex uses robotic technology to accurately and efficiently fill a variety of single-dose medication dispensing

systems.

• OnDemand Express II optimizes robotic technology for very high-speed and accurate fulfillment of single-dose

blister cards and reclaimable packaging.

Single Medication Blister Cards

We offer a wide variety of heat seal and cold seal blister cards. Heat Seal Blister Cards come in a variety of formats

that will fit various packaging requirements and require a heat sealer such as the MTS Autobond. Blister cards come in a
variety of configurations, from 14- to 90-day doses. Heat seal cards provide a stronger seal than cold seal cards, helping
pharmacists ensure consistency of the medication under nearly any environmental condition. Cold Seal Cards, also known as
pressure sensitive cards, are both efficient and reliable and do not require heat sealing equipment to be sealed. They are ideal

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for emergency orders, for heat sensitive medications or when the use of a heat sealer is not practical. Cold seal blister cards
come in a variety of configurations, from 14- to 90-day doses.

Pharmacy Printing and Labeling Solutions

Pharmacy labeling is an important part of the packaging process to ensure the right medication is packaged and

delivered to the right facility and, ultimately, the right patient. Drug specific, bar code scannable labels are affixed on many
different types of packages prior to them being dispensed.

We provide a Windows-based computer program that uses an extensive drug image database to produce a wide variety

of medication labels on multiple printers. We also provide printers and related consumables.

Multi-Medication Solutions For Use Where Patients Care For Themselves

Pharmacy Automation Systems

Our OnDemand and M-series automated solutions are designed to meet the broad needs of pharmacies to package

individual patient medication orders accurately and efficiently. These machines interface with pharmacy information systems to
obtain patient-specific prescription information which enables on-demand packaging capabilities for our larger institutional
pharmacy customers. Our current line of automation for multi-medication includes the following products:

• OnDemand 400 is an automation system for multi-medication adherence packaging. The OnDemand 400

receives patient prescriptions, constructs a filling map, fills multiple medication prescriptions into a single blister
card from an on-line array of 40 medications stored in specially calibrated dispensing canisters, prints a label and
provides an operator a sealing station.

• M5000 is a fully automated system designed specifically for multi-medication adherence packaging. The M5000
receives patient prescriptions, constructs a filling map, then uses robotic technology that fills, seals, labels and
checks the package. The M5000 minimizes human intervention in the multi-medication packaging process.

Multi-Medication Blister Cards

We offer a wide variety of heat seal and cold seal multi-medication blister cards, including products from our

acquisition of Surgichem in August 2014. Multi-medication cards allow the packaging of multiple drugs into a single blister
cavity representing a specific dosing time. Multi-medication cards are sold in a variety of formats to fit the needs of
pharmacists and patients, with the most common format providing four dosing times for each of seven days in one package.
Multi-medication adherence packages may be assembled by pharmacists by hand, or by using our pharmacy automation
systems described above.

Medication Management Solutions

Medication management systems are becoming an integral part of long-term care facilities to manage narcotics,

emergency medications and medications that are needed in a short period of time. Currently, most facilities rely on manual
systems that do not provide the level of security, accountability and efficiencies that are attainable with the use of automation.
When automation is implemented, pharmacies benefit by helping their customer facilities meet regulatory requirements and
improve the response time. Patients benefit by having access to medications immediately with minimized medication
errors. We offer specialized versions of the OmniRx medication control solution that is used by institutional pharmacies to
provide their customers with secure medication management of narcotics, emergency medication, and first doses.

Sales and Distribution

We sell our Automation and Analytics and Medication Adherence solutions primarily in the United States and Canada.

Approximately 91% of our product revenue was generated in those markets for the year ended December 31, 2014. No single
customer accounted for greater than 10% of our revenues for the years ended December 31, 2014, December 31, 2013 and
December 31, 2012. Our sales force is organized by geographic region in the United States and Canada where our sales are
primarily made direct to end user customers with the exception of some distribution of Medication Adherence consumables.
Outside the United States and Canada, we field a direct sales force for Medication Adherence products in the United Kingdom

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and Germany. For other geographies where we sell Medication Adherence products, and for all Automation and Analytics
products sold outside the United States and Canada, we sell through distributors and resellers. Our foreign operations are
discussed in Note 17, Segment Information, of the Notes to Consolidated Financial Statements and Item 7, Management’s
Discussion and Analysis of Financial Condition and Results of Operations in this annual report. Our combined direct, corporate
and international distribution sales teams consisted of approximately 206 staff members as of December 31, 2014. Nearly all of
our direct sales team members have hospital capital equipment or clinical systems experience. Our sales representatives are
generally organized to sell either the Automation and Analytics or Medication Adherence product lines. Our corporate sales
team focuses on large IDNs, group purchasing organizations ("GPOs"), and the U.S. government.

The sales cycle for our automation systems is long and can take in excess of 24 months. This is due in part to the cost

of our systems and the number of people within each healthcare facility involved in the purchasing decision. To initiate the
selling process, the sales representative generally targets the director of pharmacy, the director of materials management or
other decision makers and is responsible for educating each group within the healthcare facility about the benefits of our
solutions relative to competing methods of managing medications or medical and surgical supplies.

We have contracts with GPOs that enable us to sell our automation systems to GPO-member healthcare facilities. The

primary advantage to customers who buy our products pursuant to a GPO agreement is that they benefit from pre-negotiated
contract terms and pricing. The benefit to the GPO is the fee earned as a percentage of sales, which is paid by us. These GPO
contracts are typically for multiple years with options to renew or extend for up to two years and some of which can be
terminated by either party at any time. Our current GPO contracts include Amerinet, Inc., Federal Supply Schedule, First
Choice Management Services, Healthcare Purchasing Alliance, LLC, HealthTrust Purchasing Group, L.P., Magnet, MedAssets
Performance Management Solutions, Novation LLC, Premier Healthcare Alliance, L.P. and Resource Optimization &
Innovation, LLC. We have also contracted with the U.S. General Services Administration, allowing the Department of Veteran
Affairs, the Department of Defense and other Federal Government customers to purchase or lease our products.

We offer multi-year, non-cancelable lease payment terms to assist healthcare organizations in purchasing our systems
by reducing their cash flow requirements. We sell the majority of our multi-year lease receivables to third-party leasing finance
companies, but we also maintain a certain portion of our leases in-house.

Our field operations representatives support our sales force by providing operational and clinical expertise prior to the

close of a sale and during installation of our automation systems. This group assists the customer with the technical
implementation of our automation systems, including configuring our systems to address the specific needs of each individual
customer. After the systems are installed, on-site support is provided by our field service team and technical support group.

We offer telephone technical support through our technical support centers in Illinois and Florida. Our support centers

are staffed 24 hours a day, 365 days a year. We have found that a majority of our customers' service issues can be addressed
either over the phone or by our support center personnel utilizing their on-hand remote diagnostics tools. In addition, we utilize
remote dial-in software that monitors customer conditions on a daily basis. We offer a suite of remote monitoring features,
which proactively monitors system status and alerts service personnel to potential problems before they lead to system failure.

In addition, our international sales team handles direct sales to non-acute healthcare facilities in the United Kingdom

and Germany, and handles sales, installation and service to non-acute healthcare facilities through distribution partners in other
parts of Europe, Asia, Australia, the Middle East, South Africa, and South America. Our international sales team handles sales,
installation and service to all Automation and Analytics customers outside the U.S. and Canada through distribution partners.
Our products are available in a variety of languages including Mandarin, French, Spanish and German.

We have not sold and have no future plans to sell our products either directly or indirectly to customers located in

countries that are identified as state sponsors of terrorism by the U.S. Department of State, or those subject to economic
sanctions and export controls.

Manufacturing and Inventory

The manufacturing process for our Automation and Analytics products allows us to configure hardware and software

in unique combinations to meet a wide variety of individual customer needs. The Automation and Analytics product
manufacturing process primarily consists of the final assembly of components and testing of the completed product. Many of

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the subassemblies and components we use are provided by third-party contract manufacturers or other suppliers. We and our
partners test these subassemblies and perform inspections to assure the quality and reliability of our products. While many
components of our systems are standardized and available from multiple sources, certain components or subsystems are
fabricated by a sole supplier according to our specifications and schedule requirements. Our Medication Adherence product
manufacturing process consists of fabrication and assembly of equipment and mechanized process manufacturing of
consumables.

Our arrangements with our contract manufacturers generally set forth quality, cost and delivery requirements, as well

as manufacturing process terms, such as continuity of supply, inventory management, capacity flexibility, quality and cost
management, oversight of manufacturing and conditions for the use of our intellectual property.

Our manufacturing organization procures components and schedules production based on the backlog of customer

orders. Installation of equipment and software typically occurs between two weeks and twelve months after the initial order is
received, depending upon the customer's particular needs. We deploy a key operational strategy of operating with backlog
levels that approximate the average installation cycle of our customers, which allows us to more efficiently manage our
installation teams, improve production efficiencies, reduce inventory scrap and lower shipping costs. Shipment of consumables
typically occurs between one and fourteen days after an order is received.

Competition

The medication management and supply chain solutions market is intensely competitive. We compete directly with a
number of companies and are affected by evolving and new technologies, changes in industry standards and dynamic customer
requirements.

Our current direct competitors in the medication management and supply chain solutions market include CareFusion

Corporation (which includes Pyxis, Rowa, and PhACTs), which has entered into an agreement to be acquired by Becton
Dickenson Corporation, Aesynt Inc. (through the acquisition of McKesson Hospital Automation, Inc. by Francisco Partners),
AmerisourceBergen Corporation (through its acquisition of MedSelect, Inc. and Automed), Cerner Corporation, Talyst, Inc.,
Emerson Electronic Co. (through its acquisition of medDispense, L.P.), Swisslog Holding AG, which has entered into an
agreement to be acquired by KUKA, WaveMark Inc., ParExcellence Systems, Inc., Vanas n.v., Lawson Software, Inc. and
MACH4 Automatisierungstechnik GmbH. Our current direct competitors in the medication packaging solutions market include
Drug Package, Inc., AutoMed Technologies, Inc. (a subsidiary of AmerisourceBergen Corporation), Manchac Technologies,
LLC (through its Dosis product line) and RX Systems, Inc. in the United States and Jones Packaging Ltd., Synergy Medical
Systems, Manrex Ltd, and WebsterCare outside the United States.

We believe our products and services compare favorably with the offerings of our competitors, particularly with

respect to proprietary technological advancements, system performance, system reliability, installation, applications training,
service response time and service repair quality.

Intellectual Property and Proprietary Technology

We rely on a combination of patents, trademarks, copyright and trade secret laws, confidentiality procedures and

licensing arrangements to protect our intellectual property rights.

We pursue patent protection in the United States and foreign jurisdictions for technology that we believe to be
proprietary and that offers a potential competitive advantage for our products. Our issued patents relate to, among other things,
the use of locking and sensing lids with pharmacy drawers and the methods of restocking these drawers, and the use of guiding
lights in the open matrix, locking lid and sensing lid pharmacy drawers. These patents also apply to our unit-dose mechanism
and methods, the single-dose dispensing mechanism, the methods for restocking the single-dose drawers using exchange liners,
certain methods for loading and unloading mobile carts, the method of use of scanners with a mobile cart, and certain methods
for using radio frequency tags with storage items. Our patents expire at various times between 2015 and 2032.

All of our product system software is copyrighted and subject to the protection of applicable copyright laws. We

intend to seek additional international and U.S. patents on our technology and to seek registration of our trademarks. We have
obtained registration of Omnicell, the Omnicell logo, OmniRx, OmniCenter, OmniSupplier, OmniBuyer, SafetyStock, eMTS

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Medication Technologies, the MTS Medication Technologies logo, easy Blist, Medlocker, AccuFlex, Pandora, OnDemand,
RxMap, Suremed and OnDemand400 for RxMap. Trade secrets and other confidential information are also important to our
business. We protect our trade secrets through a combination of contractual restrictions and confidentiality and licensing
agreements.

Research and Development

We utilize industry-standard operating systems and databases, but generally develop our own application and interface
software in our research and development facilities. New product development projects are prioritized based on customer input.
Research and development takes place in Mountain View, California, Nashville, Tennessee and St. Petersburg, Florida.
Research and development expenditures were $27.8 million, $29.1 million and $23.7 million for the years ended December 31,
2014, December 31, 2013 and December 31, 2012, respectively.

Employees

We had a total of 1,236 employees as of December 31, 2014. We have rebalanced our staff as needed, at times
eliminating some functional positions and at other times adding new functional-specific positions to meet the evolving needs of
our marketplace while controlling costs. To our knowledge, none of our employees are represented by a collective bargaining
agreement, nor have we experienced any work stoppage. We believe that our employee relations are good.

Business Under Government Contracts

A number of our U.S. government-owned or government-run hospital customers sign five-year leases, with payment

terms that are subject to one-year government budget funding cycles. Failure of any of our U.S. government customers to
receive their annual funding could impair our ability to sell to these customers, or to collect payments on our existing unsold
leases. For additional information regarding these leases, see the section entitled "Risk Factors" under Part I, Item 1A below.

Financing Practices Relating to Working Capital

We assist healthcare facilities in financing their cash outlay requirements for the purchase of our systems by offering

multi-year, non-cancelable sales contracts. For additional information regarding these financing activities, see Note 1,
Summary of Significant Accounting Policies, of the Notes to Consolidated Financial Statements in this annual report.

Product Backlog

Product backlog is the dollar amount of medication and supply dispensing systems for which we have purchase orders

from our customers and for which we believe we will install, bill and gain customer acceptance within one year. Due to
industry practice that allows customers to change order configurations with limited advance notice prior to shipment and
occasional customer changes in installation schedules, we do not believe that backlog as of any particular date is necessarily
indicative of future sales. However, we do believe that backlog is an indication of a customer's willingness to install our
solutions. Our backlog was $187.7 million and $180.0 million as of December 31, 2014 and December 31, 2013, respectively.

Company Information

We were incorporated in California in 1992 under the name of Omnicell Technologies, Inc. and reincorporated in

Delaware in 2001 as Omnicell, Inc.

Available Information

We file reports and other information with the Securities and Exchange Commission ("SEC") including annual reports

on Form 10-K, quarterly reports on Form 10-Q, current reports on Form 8-K and proxy or information statements. Those
reports and statements as well as all amendments to those documents filed or furnished pursuant to Section 13(a) or 15(d) of the
Securities and Exchange Act (1) are available at the SEC's Public Reference Room at 100 F Street, N.E., Room 1580,
Washington, DC 20549, (2) are available at the SEC's internet site (www.sec.gov), which contains reports, proxy and
information statements and other information regarding issuers that file electronically with the SEC and (3) are available free of
charge through our website as soon as reasonably practicable after electronic filing with, or furnishing to, the SEC. You may

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obtain information on the operation of the Public Reference Room by calling the SEC at 1-800-SEC-0330. Our website address
is www.omnicell.com. Information on our website is not incorporated by reference nor otherwise included in this report.

Executive Officers of the Registrant

The following table sets forth certain information about our executive officers as of the date of this annual report:

Name

Randall A. Lipps
J. Christopher Drew

Robin G. Seim

Dan S. Johnston

Nhat H. Ngo

Jorge R. Taborga

Age
57
49

Position

President, Chief Executive Officer, and Chairman of the Board of Directors
Executive Vice President, Sales and Marketing

Executive Vice President Finance, International and Manufacturing, Chief
Financial Officer

Executive Vice President and Chief Legal and Administrative Officer

Executive Vice President, Strategy and Business Development

Executive Vice President, Engineering

Randall A. Lipps was named Chief Executive Officer and President of Omnicell in October 2002. Mr. Lipps has

served as Chairman of the Board and a Director of Omnicell since founding Omnicell in September 1992. Mr. Lipps received
both a B.S. in economics and a B.B.A. from Southern Methodist University.

J. Christopher Drew joined Omnicell in April 1994 and was named Senior Vice President, Operations in January 2005.

In January 2009, Mr. Drew was named Senior Vice President, Field Operations. In March 2012, Mr. Drew was named
Executive Vice President, Field Operations. In February 2015, Mr. Drew was named Executive Vice President, Sales and
Marketing. From April 1994 to January 2005, Mr. Drew served in various management positions with Omnicell, including Vice
President of Branded Solutions and Director of Corporate Development. Mr. Drew received a B.A. in economics from Amherst
College and an M.B.A. from the Stanford Graduate School of Business.

Robin G. Seim joined Omnicell in February 2006 as Vice President and was named Chief Financial Officer in March

2006. In January 2009, Mr. Seim was named Chief Financial Officer and Vice President Finance, Administration and
Manufacturing. In March 2012, Mr. Seim was named Chief Financial Officer and Executive Vice President Finance,
Administration and Manufacturing. In February 2015, Mr. Seim was named Chief Financial Officer and Executive Vice
President, Finance, International and Manufacturing. Prior to joining Omnicell, Mr. Seim served as Chief Financial Officer of
several technology companies, including Villa Montage Systems, Inc. from 1999 to 2001, Candera, Inc. from 2001 to 2004 and
Mirra, Inc., in 2005. Prior to 1999, Mr. Seim held a number of management positions with Nortel Networks, Bay Networks,
and IBM. Mr. Seim received a B.S. in accounting from California State University, Sacramento.

Dan S. Johnston joined Omnicell in November 2003 as Vice President and General Counsel. In March 2012, Mr.

Johnston was named Executive Vice President and General Counsel. In February 2015, Mr. Johnston was named Executive
Vice President and Chief Legal and Administrative Officer. From April 1999 to November 2003, Mr. Johnston was Vice
President and General Counsel at Be, Inc., a software company. From September 1994 to March 1999, Mr. Johnston was an
attorney with the law firm Cooley LLP. Mr. Johnston received a B.S. in computer information systems from Humboldt State
University and a J.D. from the Santa Clara University School of Law.

Nhat H. Ngo joined Omnicell in November 2008 as Vice President of Strategy and Business Development. In March

2012, Mr. Ngo was named Executive Vice President, Strategy and Business Development. From January 2007 to October 2008,
Mr. Ngo served as Vice President of Business Development and Licensing for a business unit of Covidien, a global healthcare
products company. From June 1999 to April 2006, Mr. Ngo worked at BriteSmile, Inc., a direct-to-consumer aesthetic
technology company and served in a variety of senior leadership positions in marketing, sales, operations, strategic planning
and corporate development. From September 1997 to June 1999, Mr. Ngo practiced corporate law at Shaw Pittman, LLP.
Mr. Ngo received a B.S. in commerce, with a concentration in finance, from the University of Virginia McIntire School of
Commerce and a J.D. from the University of Virginia School of Law.

Jorge R. Taborga joined Omnicell in July 2007 as Vice President and Chief Information Officer. In February of 2013,

Mr. Taborga was named Executive Vice President, Engineering. From January 2009 to February 2013, Mr. Taborga was Vice

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President of Manufacturing, Quality and Information Technology. Prior to joining Omnicell, Mr. Taborga held a number of
executive positions with Bay Networks and Quantum, and ran his own management consulting company. He also held
executive roles in two cloud computing companies, fusionOne and Terrasping. Mr. Taborga's earlier career includes senior roles
in product development with ROLM Systems and Thomas-Conrad. Mr. Taborga received B.S. and M.S. degrees in Computer
Science from Texas A&M University. He is currently pursuing a Ph.D. in Organizational Systems at Saybrook University.

ITEM 1A. RISK FACTORS

We have identified the following risks and uncertainties that may have a material adverse effect on our business,

financial condition or results of operations. Our business faces significant risks and the risks described below may not be the
only risks we face. Additional risks not presently known to us or that we currently believe are immaterial may also significantly
impair our business operations. If any of these risks occur, our business, results of operations or financial condition could suffer
and the market price of our common stock could decline.

Unfavorable economic and market conditions, a decreased demand in the capital equipment market and uncertainty
regarding the rollout of government legislation in the healthcare industry could adversely affect our operating results.

Customer demand for our products is significantly linked to the strength of the economy. If decreases in demand for

capital equipment caused by weak economic conditions and decreased corporate and government spending, including any
effects of fiscal budget balancing at the federal level, deferrals or delays of capital equipment projects, longer time frames for
capital equipment purchasing decisions or generally reduced expenditures for capital solutions occurs, we will experience
decreased revenues and lower revenue growth rates and our operating results could be materially and adversely affected.

Additionally, as the U.S. Federal government implements healthcare reform legislation, and as Congress, regulatory

agencies and other state governing organizations continue to review and assess additional healthcare legislation and regulations,
there may be an impact on our business. Healthcare facilities may decide to postpone or reduce spending until the implications
of such healthcare enactments are more clearly understood, which may affect the demand for our products and harm our
business.

The medication management and supply chain solutions market is highly competitive and we may be unable to compete
successfully against new entrants and established companies with greater resources and/or existing business relationships
with our current and potential customers.

The medication management and supply chain solutions market is intensely competitive. We expect continued and

increased competition from current and future competitors, many of which have significantly greater financial, technical,
marketing and other resources than we do. Our current direct competitors in the medication management and supply chain
solutions market include CareFusion Corporation (which includes Pyxis, Rowa, and PhACTs), which has entered into an
agreement to be acquired by Becton Dickenson Corporation, Aesynt Inc. (through the acquisition of McKesson Hospital
Automation, Inc. by Francisco Partners), AmerisourceBergen Corporation (through its acquisition of MedSelect, Inc. and
Automed), Cerner Corporation, Talyst, Inc., Emerson Electronic Co. (through its acquisition of medDispense, L.P.), Swisslog
Holding AG, which has entered into an agreement to be acquired by KUKA, WaveMark Inc., ParExcellence Systems, Inc.,
Vanas n.v., Lawson Software, Inc. and MACH4 Automatisierungstechnik GmbH. Our current direct competitors in the
medication packaging solutions market include Drug Package, Inc., AutoMed Technologies, Inc. (a subsidiary of
AmerisourceBergen Corporation), Manchac Technologies, LLC (through its Dosis product line) and RX Systems, Inc. in the
United States, Jones Packaging Ltd., Synergy Medical Systems, Manrex Ltd, and WebsterCare outside the United States.

The competitive challenges we face in the medication management and supply chain solutions market include, but are

not limited to, the following:

•

certain competitors may offer or have the ability to offer a broader range of solutions in the marketplace that we
are unable to match;

certain competitors may develop alternative solutions to the customer problems our products are designed to solve
that may provide a better customer outcome or a lower cost of operation;

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•

certain competitors may develop new features or capabilities for their products not previously offered that could
compete directly with our products;

competitive pressures could result in increased price competition for our products and services, fewer customer
orders and reduced gross margins, any of which could harm our business;

current and potential competitors may make strategic acquisitions or establish cooperative relationships among
themselves or with third parties, including larger, more established healthcare supply companies, such as the
pending acquisition of CareFusion Corporation by Becton Dickenson Corporation, thereby increasing their ability
to develop and offer a broader suite of products and services to address the needs of our prospective customers;

• our competitive environment is currently experiencing a significant degree of consolidation which could lead to
competitors developing new business models that require us to adapt how we market, sell or distribute our
products;

• other established or emerging companies may enter the medication management and supply chain solutions

market with products and services that are preferred by our current and potential customers based on factors such
as features, capabilities or cost;

• our competitors may develop, license or incorporate new or emerging technologies or devote greater resources to

the development, promotion and sale of their products and services than we do;

•

certain competitors have greater brand name recognition and a more extensive installed base of medication and
supply dispensing systems or other products and services than we do, and such advantages could be used to
increase their market share;

certain competitors may have existing business relationships with our current and potential customers, which may
cause these customers to purchase medication and supply dispensing systems or automation solutions from these
competitors; and

• our competitors may secure products and services from suppliers on more favorable terms or secure exclusive

arrangements with suppliers or buyers that may impede the sales of our products and services.

Any reduction in the demand for or adoption of our medication and supply systems, related services, or consumables would
reduce our revenues.

Our medication and supply dispensing systems represent only one approach to managing the distribution of
pharmaceuticals and supplies at acute healthcare facilities and our medication packaging systems represent only one way of
managing medication distribution at non-acute care facilities. A significant portion of domestic and international healthcare
facilities still use traditional approaches in some form that do not include fully automated methods of medication and supply
management. As a result, we must continuously educate existing and prospective customers about the advantages of our
products, which requires significant sales efforts and can cause longer sales cycles. Despite our significant efforts and extensive
time commitments in sales to healthcare facilities, we cannot be assured that our efforts will result in sales to these customers.

In addition, our medication and supply dispensing systems and our more complex automated packaging systems

typically represent a sizable initial capital expenditure for healthcare organizations. Changes in the budgets of these
organizations and the timing of spending under these budgets can have a significant effect on the demand for our medication
and supply dispensing systems and related services. These budgets are often supported by cash flows that can be negatively
affected by declining investment income and influenced by limited resources, increased operational and financing costs,
macroeconomic conditions such as unemployment rates and conflicting spending priorities among different departments. Any
decrease in expenditures by healthcare facilities or increased financing costs could decrease demand for our medication and
supply dispensing systems and related services and reduce our revenues.

Changing customer requirements could decrease the demand for our products and services and our new product solutions
may not achieve market acceptance.

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The medication management and supply chain solutions market is characterized by evolving technologies and industry

standards, frequent new product introductions and dynamic customer requirements that may render existing products obsolete
or less competitive. The medication management and supply chain solutions market could erode rapidly due to unforeseen
changes in the features and functions of competing products, as well as the pricing models for such products. Our future
success will depend in part upon our ability to enhance our existing products and services and to develop and introduce new
products and services to meet changing customer requirements. The process of developing products and services such as those
we offer is extremely complex and is expected to become increasingly more complex and expensive in the future as new
technologies are introduced. If we are unable to enhance our existing products or develop new products to meet changing
customer requirements, and bring such enhancements and products to market in a timely manner, demand for our products
could decrease.

We cannot provide assurance that we will be successful in marketing any new products or services that we introduce,

that new products or services will compete effectively with similar products or services sold by our competitors, or that the
level of market acceptance of such products or services will be sufficient to generate expected revenues and synergies with our
other products or services. Deployment of new products or services often requires interoperability with other Omnicell products
or services as well as with healthcare facilities' existing information management systems. If these products or services fail to
satisfy these demanding technological objectives, our customers may be dissatisfied and we may be unable to generate future
sales.

The healthcare industry faces financial constraints and consolidation that could adversely affect the demand for our
products and services.

The healthcare industry has faced, and will likely continue to face, significant financial constraints. U.S. government

legislation such as the American Recovery and Reinvestment Act of 2009, the Patient Protection and Affordable Care Act of
2010, the Budget Control Act of 2011, and other health reform legislation may cause customers to postpone purchases of our
products due to reductions in federal healthcare program reimbursement rates and/or needed changes to their operations in
order to meet the requirements of legislation. Our automation solutions often involve a significant financial commitment from
our customers and, as a result, our ability to grow our business is largely dependent on our customers' capital and operating
budgets. To the extent legislation promotes spending on other initiatives or healthcare providers spending declines or increases
more slowly than we anticipate, demand for our products and services could decline.

Many healthcare providers have consolidated to create larger healthcare delivery organizations in order to achieve

greater market power. If this consolidation continues, it would increase the size of certain target customers, which could
increase the cost, effort and difficulty in selling our products to such target customers, or could cause our existing customers or
potential new customers to begin utilizing our competitors' products if such customers are acquired by healthcare providers that
prefer our competitors' products to ours. In addition, the resulting organizations could have greater bargaining power, which
may lead to price erosion.

We may not be able to successfully integrate acquired businesses or technologies into our existing business, which could
negatively impact our operating results.

As a part of our business strategy we may seek to acquire businesses, technologies or products in the future. For

example, on August 22, 2014, we acquired Surgichem Limited from Bupa. We cannot provide assurance that any acquisition or
any future transaction we complete will result in long-term benefits to us or our stockholders, or that our management will be
able to integrate or manage the acquired business effectively. Acquisitions entail numerous risks, including difficulties
associated with the integration of operations, technologies, products and personnel that, if realized, could harm our operating
results. Risks related to potential acquisitions include, but are not limited to:

• difficulties in combining previously separate businesses into a single unit and the complexity of managing a more

dispersed organization as sites are acquired;

•

complying with international labor laws that may restrict our ability to right-size organizations and gain synergies
across acquired operations;

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•

the substantial costs that may be incurred and the substantial diversion of management's attention from day-to-day
business when evaluating and negotiating such transactions and then integrating an acquired business;

• discovery, after completion of the acquisition, of liabilities assumed from the acquired business or of assets
acquired that are broader in scope and magnitude or are more difficult to manage than originally assumed;

•

failure to achieve anticipated benefits such as cost savings and revenue enhancements;

• difficulties related to assimilating the products or key personnel of an acquired business;

•

failure to understand and compete effectively in markets in which we have limited previous experience; and

• difficulties in integrating newly acquired products and solutions into a logical offering that our customers

understand and embrace.

Successful integration of acquired operations, products and personnel into Omnicell may place a significant burden on

the combined company's management and internal resources. We may also experience difficulty in effectively integrating the
different cultures and practices of any acquired entity. The challenges of integrating acquired entities could disrupt the
combined company's ongoing business, distract its management focus from other opportunities and challenges, and increase
expenses and working capital requirements. The diversion of management attention and any difficulties encountered in the
transition and integration process could harm our business, financial condition and operating results.

Demand for our consumable medication packages is time-sensitive and if we are not able to supply the demand from our
institutional and retail pharmacy customers on schedule and with quality packaging products, they may utilize alternative
means to distribute medications to their customers.

Approximately 17% of our revenue is generated from the sale of consumable medication packages, which are

produced in our St. Petersburg, Florida facilities on a continuous basis and shipped to our institutional pharmacy and retail
pharmacy customers shortly before they are required by those customers. The demands placed on institutional pharmacies and
retail pharmacies by their customers represent real time requirements of those customers. Our customer agreements for the sale
of consumable medication packages are typically short-term in nature and typically do not include any volume commitments on
the part of the customer. Although our packaging may be considered the preferred method of maintaining control of
medications during the medication distribution and administration process, institutional and retail pharmacies have alternative
methods of distributing medications, including bulk and alternative packaging, and medication adherence packaging may be
supplied by our competitors. To the extent that we are unable to supply quality packaging to our customers in a timely manner,
that demand will be met via alternative distribution methods, including consumable medication packaging sold by our
competitors, and our revenue will decline. Any disruption in the production capabilities of our St. Petersburg facilities will
adversely affect our ability to ship our consumable medication packages and would reduce our revenue.

Our international operations may subject us to additional risks that can adversely affect our operating results.

We currently have operations outside of the United States, including sales efforts centered in Canada, Europe, the

Middle East and Asia-Pacific regions and supply chain efforts in Asia. We intend to continue to expand our international
operations, particularly in certain markets that we view as strategic, including China and the Middle East. Our international
operations subject us to a variety of risks, including:

• our reliance on distributors for the sale and post-sale support of our automated dispensing systems outside the

United States and Canada;
the difficulty of managing an organization operating in various countries;

•
• political sentiment against international outsourcing of production;
•

reduced protection for intellectual property rights, particularly in jurisdictions that have less developed intellectual
property regimes;
changes in foreign regulatory requirements;
the requirement to comply with a variety of international laws and regulations, including privacy, labor, import,
export, environmental standards, tax, anti-bribery and employment laws and changes in tariff rates;

•
•

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•
•

fluctuations in currency exchange rates and difficulties in repatriating funds from certain countries;
additional investment, coordination and lead-time necessary to successfully interface our automation solutions
with the existing information systems of our customers or potential customers outside of the United States; and

• political unrest, terrorism and the potential for other hostilities in areas in which we have facilities.

If we are unable to anticipate and address these risks properly, our business or operating results will be harmed.

If we experience delays in installations of our medication and supply dispensing systems or our more complex medication
packaging systems, resulting in delays in our ability to recognize revenue, our competitive position, results of operations and
financial condition could be harmed.

The purchase of our medication and supply dispensing systems or our more complex medication packaging systems is
often part of a customer's larger initiative to re-engineer its pharmacy and their distribution and materials management systems.
As a result, our sales cycles are often lengthy. The purchase of our systems often entail larger strategic purchases by customers
that frequently require more complex and stringent contractual requirements and generally involve a significant commitment of
management attention and resources by prospective customers. These larger and more complex transactions often require the
input and approval of many decision-makers, including pharmacy directors, materials managers, nurse managers, financial
managers, information systems managers, administrators, lawyers and boards of directors. For these and other reasons, the sales
cycle associated with the sale of our medication and supply dispensing systems is often lengthy and subject to a number of
delays over which we have little or no control. A delay in, or loss of, sales of our medication and supply dispensing systems
could have an adverse effect upon our operating results and could harm our business.

In addition, and in part as a result of the complexities inherent in larger transactions, the time between the purchase

and installation of our systems can range from two weeks to one year. Delays in installation can occur for reasons that are often
outside of our control. We have also experienced fluctuations in our customer and transaction size mix, which makes our ability
to forecast our product bookings more difficult. Because we recognize revenue for our medication and supply dispensing
systems and our more complex medication packaging systems only upon installation at a customer's site, any delay in
installation by our customers will also cause a delay in the recognition of the revenue for that system.

Government regulation of the healthcare industry could reduce demand for our products, or substantially increase the cost
to produce our products.

The manufacture and sale of our current products are not regulated by the United States Food and Drug

Administration, or the Drug Enforcement Administration ("DEA"). However, our current products, and any future products,
may be regulated in the future by these or other federal agencies due to future legislative and regulatory initiatives or reforms.
Direct regulation of our business and products by the FDA, DEA or other federal agencies could substantially increase the cost
to produce our products and increase the time required to bring those products to market, reduce the demand for our products
and reduce our revenues. In addition, healthcare providers and facilities that use our equipment and dispense controlled
substances are subject to regulation by the DEA. The failure of these providers and facilities to comply with DEA requirements,
including the Controlled Substances Act and its implementing regulations, could reduce demand for our products and harm our
competitive position, results of operations and financial condition. Pharmacies are regulated by individual state boards of
pharmacy that issue rules for pharmacy licensure in their respective jurisdictions. State boards of pharmacy do not license or
approve our medication and supply dispensing systems; however, pharmacies using our equipment are subject to state board
approval. The failure of such pharmacies to meet differing requirements from a significant number of state boards of pharmacy
could decrease demand for our products and harm our competitive position, results of operations and financial condition.
Similarly, hospitals must be accredited by The Joint Commission in order to be eligible for Medicaid and Medicare funds. The
Joint Commission does not approve or accredit medication and supply dispensing systems; however, disapproval of our
customers' medication and supply dispensing management methods and their failure to meet The Joint Commission
requirements could decrease demand for our products and harm our competitive position, results of operations and financial
condition.

While we have implemented a Privacy and Use of Information Policy and adhere to established privacy principles, use

of customer information guidelines and related federal and state statutes, we cannot assure you that we will be in compliance
with all federal and state healthcare information privacy and security laws that we are directly or indirectly subject to,

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including, without limitation, the Health Insurance Portability and Accountability Act of 1996. Among other things, this
legislation required the Secretary of Health and Human Services to adopt national standards governing the conduct of certain
electronic health information transactions and protecting the privacy and security of personally identifiable health information
maintained or transmitted by "covered entities," which include pharmacies and other healthcare providers with which we do
business.

The standards adopted to date include, among others, the "Standards for Privacy of Individually Identifiable Health
Information," which restrict the use and disclosure of personally identifiable health information by covered entities, and the
"Security Standards," which require covered entities to implement administrative, physical and technical safeguards to protect
the integrity and security of certain electronic health information. Under HIPAA, we are considered a "business associate" in
relation to many of our customers that are covered entities, and as such, most of these customers have required that we enter
into written agreements governing the way we handle and safeguard certain patient health information we may encounter in
providing our products and services and may impose liability on us for failure to meet our contractual obligations. Further,
pursuant to changes in HIPAA under the American Recovery and Reinvestment Act of 2009 ("ARRA"), we are now also
covered under HIPAA similar to other covered entities and in some cases, subject to the same civil and criminal penalties as a
covered entity. A number of states have also enacted privacy and security statutes and regulations that, in some cases, are more
stringent than HIPAA and may also apply directly to us. If our past or present operations are found to violate any of these laws,
we may be subject to fines, penalties and other sanctions.

During November 2012, an Omnicell electronic device containing medication dispensing cabinet log files from three

health system customers was stolen from an Omnicell employee's locked vehicle. The files on this device contained certain
protected patient health information related to medication dispensing transactions from our medication dispensing cabinets over
a one to three-week period, downloaded by the employee while troubleshooting software for the hospitals. This loss resulted in
a putative class action complaint being filed against us and certain of our customers in the United States District Court for the
District of New Jersey in March 2013 alleging breach of state security notification laws, violations of state consumer fraud
laws, fraud, negligence and conspiracy relating to the theft of an Omnicell electronic device containing medication dispensing
cabinet log files, including certain patient health information, described above and subsequent notification of this unauthorized
disclosure of personal health information. In December 2013, the court issued an order dismissing the plaintiff's complaint
without prejudice. The plaintiff failed to file an appeal of the court's decision by the January 27, 2014 deadline. There is no
guarantee that, if we are involved in any similar litigation in the future, such an outcome will result. Any similar unauthorized
disclosure of personal health information could cause us to experience contractual indemnification obligations under business
associate agreements with certain customers, litigation against us, reputational harm and a reduction in demand from our
customers. To the extent that this disclosure is deemed to be a violation of HIPAA or other privacy or security laws, we may be
subject to significant fines, penalties and other sanctions. As of the date of this Form 10-K filing, the Company has not received
correspondence from the Office for Civil Rights of the U.S. Department of Health & Human Services with respect to this
matter.

In addition, we cannot predict the potential impact of future HIPAA standards and other federal and state privacy and

security laws that may be enacted at any time on our customers or on Omnicell. These laws could restrict the ability of our
customers to obtain, use or disseminate patient information, which could reduce the demand for our products or force us to
redesign our products in order to meet regulatory requirements.

Covenants in our credit agreement restrict our business and operations in many ways and if we do not effectively manage
our compliance with these covenants, our financial conditions and results of operations could be adversely affected.

In September 2013, we entered into a $75 million revolving credit facility pursuant to a Credit Agreement, by and
among Omnicell, Wells Fargo Bank, National Association, as administrative agent, and the lenders from time to time party
thereto (“Credit Agreement”). In November 2014, we amended the Credit Agreement to increase the number of shares of
common stock that may be repurchased pursuant to stock repurchase programs authorized by our Board of Directors. The
Credit Agreement contains various customary covenants that limit our ability and/or our subsidiaries’ ability to, among other
things:

•

incur or assume liens or additional debt or provide guarantees in respect of obligations or other persons;

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issue redeemable preferred stock;

•
• pay dividends or distributions or redeem or repurchase capital stock;
• prepay, redeem or repurchase certain debt;
• make loans, investments, acquisitions (including acquisitions of exclusive licenses) and capital expenditures;
•
•
•
•

enter into agreements that restrict distributions from our subsidiaries;
sell assets and capital stock of our subsidiaries;
enter into certain transactions with affiliates; and
consolidate or merge with or into, or sell substantially all of our assets to, another person.

The Credit Agreement also includes, among other financial covenants, financial covenants that require us to maintain a

maximum total leverage ratio and minimum fixed charge coverage ratio. Our ability to comply with these financial covenants
may be affected by events beyond our control. Our failure to comply with any of the covenants could result in a default under
the Credit Agreement, which could permit the administrative agent or the lenders to declare all or part of any outstanding
borrowings to be immediately due and payable, or to refuse to permit additional borrowings under the revolving credit facility,
which could restrict our operations, particularly our ability to respond to changes in our business or to take specified actions to
take advantage of certain business opportunities that may be presented to us. In addition, if we are unable to repay those
amounts, the administrative agent and the lenders under the Credit Agreement could proceed against the collateral granted to
them to secure that debt, which would seriously harm our business.

If we are unable to recruit and retain skilled and motivated personnel, our competitive position, results of operations and
financial condition could be harmed.

Our success is highly dependent upon the continuing contributions of our key management, sales, technical and

engineering staff. We believe that our future success will depend upon our ability to attract, train and retain highly skilled and
motivated personnel. As more of our products are installed in increasingly complex environments, greater technical expertise
will be required. As our installed base of customers increases, we will also face additional demands on our customer service
and support personnel, requiring additional resources to meet these demands. We may experience difficulty in recruiting
qualified personnel. Competition for qualified technical, engineering, managerial, sales, marketing, financial reporting and
other personnel can be intense and may not be successful in attracting and retaining qualified personnel. Competitors have in
the past attempted, and may in the future attempt, to recruit our employees.

In addition, we have historically used stock options, restricted stock units and other forms of equity compensation as

key components of our employee compensation program in order to align employees' interests with the interests of our
stockholders, encourage employee retention and provide competitive compensation packages. The effect of managing share-
based compensation expense and minimizing shareholder dilution from the issuance of new shares may make it less favorable
for us to grant stock options, restricted stock units or other forms of equity compensation, to employees in the future. In order
to continue granting equity compensation at competitive levels, we must seek stockholder approval for any increases to the
number of shares reserved for issuance under our equity incentive plans, such as the share increase for which we obtained
approval at our 2013 Annual Meeting of Stockholders, and we cannot assure you that we will receive such approvals in the
future. Any failure to receive approval for current or future proposed increases could prevent us from granting equity
compensation at competitive levels and make it more difficult to attract, retain and motivate employees. Further, to the extent
that we expand our business or product lines through the acquisition of other businesses, any failure to receive any such
approvals could prevent us from securing employment commitments from such newly acquired employees. Failure to attract
and retain key personnel could harm our competitive position, results of operations and financial condition.

In the past, we have experienced substantial fluctuations in customer demand, and we cannot be sure that we will be able to
respond proactively to future changes in customer demand.

Our ability to adjust to fluctuations in our revenue while still achieving or sustaining profitability is dependent upon
our ability to manage costs and control expenses. If our revenue increases or decreases rapidly, we may not be able to manage
these changes effectively. Future growth is dependent on the continued demand for our products, the volume of installations we
are able to complete, our ability to continue to meet our customers' needs and provide a quality installation experience and our
flexibility in manpower allocations among customers to complete installations on a timely basis.

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Regarding our expenses, our ability to control expense is dependent on our ability to continue to develop and leverage
effective and efficient human and information technology systems, our ability to gain efficiencies in our workforce through the
local and worldwide labor markets and our ability to grow our outsourced vendor supply model. Our expense growth rate may
equal or exceed our revenue growth rate if we are unable to streamline our operations, or fail to reduce the costs or increase the
margins of our products. In addition, we may not be able to reduce our expenses to keep pace with any reduction in our
revenue, which could harm our results of operations and financial position.

If we are unable to successfully interface our automation solutions with the existing information systems of our customers,
they may choose not to use our products and services.

For healthcare facilities to fully benefit from our automation solutions, our systems must interface with their existing

information systems. This may require substantial cooperation, incremental investment and coordination on the part of our
customers and may require coordination with third-party suppliers of the existing information systems. There is little
uniformity in the systems currently used by our customers, which complicates the interfacing process. If these systems are not
successfully interfaced, our customers could choose not to use or to reduce their use of our automation solutions, which would
harm our business. Also, these information systems are impacted by regulatory forces, such as the HITECH Act,
Meaningful Use Stages, and HIPAA Omnibus Rules, and may evolve their interoperability functionality accordingly. We expect
to comply with the mandatory standards and certifications that enable us to continuously interoperate with partner information
system, but such symbiotic evolution in a changing regulatory environment can at times create an execution risk.

Additionally, our competitors may enter into agreements with providers of hospital information management systems
that are designed to increase the interoperability of their respective products. To the extent our competitors are able to increase
the interoperability of their products with those of the major hospital information systems providers, customers who utilize
such information systems may choose not to use our products and services. In addition, hospital information systems providers
may choose to develop their own solutions that could compete with ours. Furthermore, we expect the importance of
interoperability to increase in the next few years. Regulations such as the HITECH Act Meaningful Use Stage 3 are expected to
heavily focus on evidence and outcomes. Given our role in care delivery process, the data generated by our products may be a
key input for assessing and reporting on clinical outcomes. This may elevate interoperability with information systems to a
relative importance to our customers creating a business opportunity and risk.

Our failure to protect our intellectual property rights could negatively affect our ability to compete.

Our success depends in part on our ability to obtain patent protection for technology and processes and our ability to

preserve our trademarks, copyrights and trade secrets. We have pursued patent protection in the United States and foreign
jurisdictions for technology that we believe to be proprietary and for technology that offers us a potential competitive
advantage for our products. We intend to continue to pursue such protection in the future. Our issued patents relate to various
features of our medication and supply dispensing systems and our packaging systems. We cannot assure you that we will file
any patent applications in the future, and that any of our patent applications will result in issued patents or that, if issued, such
patents will provide significant protection for our technology and processes. As an example, in September 2014, an action was
brought against us, to, among other matters, correct the inventorship of certain patents owned by us. For additional details, see
Note 13, Contingencies, in this annual report. Furthermore, we cannot assure you that others will not develop technologies that
are similar or superior to our technology or that others will not design around the patents we own. All of our system software is
copyrighted and subject to the protection of applicable copyright laws. Despite our efforts to protect our proprietary rights,
unauthorized parties may attempt to copy aspects of our products or obtain and use information that we regard as proprietary,
which could harm our competitive position.

Our quarterly operating results may fluctuate and may cause our stock price to decline.

Our quarterly operating results may vary in the future depending on many factors that include, but are not limited to,

the following:

• our ability to successfully install our products on a timely basis and meet other contractual obligations necessary

to recognize revenue;

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•

•
•
•

•

the size, product mix and timing of orders for our medication and supply dispensing systems, and our medication
packaging systems, and their installation and integration;
the overall demand for healthcare medication management and supply chain solutions;
changes in pricing policies by us or our competitors;
the number, timing and significance of product enhancements and new product announcements by us or our
competitors;
the timing and significance of any acquisition or business development transactions that we may consider or
negotiate and the revenues, costs and earnings that may be associated with these transactions;
the relative proportions of revenues we derive from products and services;
fluctuations in the percentage of sales attributable to our international business;

•
•
• our customers' budget cycles;
•
•
• our ability to generate cash from our accounts receivable on a timely basis;
•
•
• macroeconomic and political conditions, including fluctuations in interest rates, tax increases and availability of

changes in our operating expenses and our ability to stabilize expenses;
expenses incurred to remediate product quality or safety issues;

the performance of our products;
changes in our business strategy;

credit markets; and

• volatility in our stock price and its effect on equity-based compensation expense.

Due to all of these factors, our quarterly revenues and operating results are difficult to predict and may fluctuate,

which in turn may cause the market price of our stock to decline.

If we are unable to maintain our relationships with group purchasing organizations or other similar organizations, we may
have difficulty selling our products and services to customers represented by these organizations.

A number of group purchasing organizations, including Amerinet, Inc., Federal Supply Schedule, First Choice
Management Services, Healthcare Purchasing Alliance, LLC, HealthTrust Purchasing Group, L.P., Magnet, MedAssets
Performance Management Solutions, Novation LLC, Premier Healthcare Alliance, L.P. and Resource Optimization &
Innovation, LLC have negotiated standard contracts for our products on behalf of their member healthcare organizations.
Members of these group purchasing organizations may purchase under the terms of these contracts, which obligate us to pay
the group purchasing organization a fee. We have also contracted with the United States General Services Administration,
allowing the Department of Veteran Affairs, the Department of Defense and other Federal Government customers to purchase
our products. These contracts enable us to more readily sell our products and services to customers represented by these
organizations. Some of our contracts with these organizations are terminable at the convenience of either party. The loss of any
of these relationships could impact the breadth of our customer base and could impair our ability to meet our revenue targets or
increase our revenues. These organizations may not renew our contracts on similar terms, if at all, and they may choose to
terminate our contracts before they expire, any of which could cause our revenues to decline.

If we are unable to maintain our relationships with major institutional pharmacies, we may experience a decline in the sales
of blister cards and other consumables sold to these customers.

The institutional pharmacy market consists of significant national suppliers of medications to non-acute care facilities,

smaller regional suppliers, and very small local suppliers. Although none of these customers comprised more than 10% of our
total revenues for the year ended December 31, 2014, they may, in some periods, comprise up to 16% of our consumables
revenues. If these larger national suppliers were to purchase consumable blister card components from alternative sources, or if
alternatives to blister cards were used for medication control, our revenues would decline.

Our failure to maintain effective internal control over financial reporting in accordance with Section 404 of the Sarbanes-
Oxley Act of 2002 could cause our stock price to decline.

Section 404 of the Sarbanes-Oxley Act of 2002 and the related rules and regulations of the SEC require annual

management assessments of the effectiveness of our internal control over financial reporting and a report by our independent
registered public accounting firm attesting to the effectiveness of internal control. If we fail to maintain effective internal

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control over financial reporting, as such standards are modified, supplemented or amended from time to time, we may not be
able to ensure that we can conclude on an ongoing basis that we have effective internal control over financial reporting.

If the market price of our common stock continues to be highly volatile, the investment value of our common stock may
decline.

Our common stock traded between $24.85 and $34.00 per share during the year ended December 31, 2014. The

market price for shares of our common stock has been and may continue to be highly volatile. In addition, our announcements
or external events may have a significant impact on the market price of our common stock. These announcements or external
events may include:

changes in our operating results;

•
• developments in our relationships with corporate customers;
•
•
•
• general economic and market conditions.

changes in the ratings of our common stock by securities analysts;
announcements by us or our competitors of technological innovations or new products;
announcements by us or our competitors of acquisitions of businesses, products or technologies; or

Furthermore, the stock market as a whole from time to time has experienced extreme price and volume fluctuations,
which have particularly affected the market prices for technology companies. These broad market fluctuations may cause the
market price of our common stock to decline irrespective of our performance. Also, sales of substantial amounts of our
common stock in the public market could lower the market price of our common stock.

In addition, stockholders have initiated class action lawsuits against companies following periods of volatility in the

market prices of these companies’ stock. On March 19, 2015, a putative class action lawsuit was filed against Omnicell and two
of our executive officers (the “Defendants”) in the U.S. District Court for the Northern District of California. The complaint
purports to assert claims on behalf of a class of purchasers of Omnicell stock between May 2, 2014 and March 2, 2015. The
complaint alleges that Defendants violated Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 by purportedly
making false and misleading statements regarding the existence of a “side letter” arrangement and the adequacy of internal
controls that allegedly resulted in false and misleading financial statements. While we believe that the claims have no merit and
will defend the lawsuit vigorously, such litigation could cause us to incur substantial costs and divert management’s attention
and resources.

Circumstances may arise that could prevent the timely reporting of our financial information, which could harm our stock
price and quotation on the NASDAQ Global Select Market.

On March 17, 2015, we announced that we were delaying the filing of this Annual Report on Form 10-K for the year

ended December 31, 2014 beyond the automatic 15-day extension period permitted under the rules of the Securities and
Exchange Commission because of the internal investigation that we commenced following receipt of a notice from an Omnicell
employee on February 27, 2015 alleging, among other matters, the existence of a “side letter” arrangement with an Omnicell
customer for certain discounts and Omnicell products that were to be provided at no cost, but which were not reflected in the
final invoices paid by such customer.

Because we were unable to timely file this Annual Report on Form 10-K, on March 18, 2015, we received an expected

written notification (the “Notice”) from the NASDAQ OMX Group, Inc. (“Nasdaq”) indicating that Omnicell was not in
compliance with Nasdaq Listing Rule 5250(c)(1) for continued listing, due to the delay in filing this Annual Report on Form
10-K for the period ended December 31, 2014 beyond the extended filing due date. Under the Nasdaq continued listing rules,
we had 60 calendar days from the date of the letter to either file this Annual Report on Form 10-K or submit a plan to regain
compliance.

During the period between the date this Annual Report on Form 10-K was due and the date of this filing, our stock

price has experienced some volatility. We have concluded the investigation causing the delay of the filing of this Annual Report
on Form 10-K. Even though the results of the investigation led the Company to determine that effective internal control over
financial reporting was maintained in all material respects and that there are no changes required to be made to the Company’s
Consolidated Financial Statements, we cannot assure you that similar circumstances will not arise in the future that will cause

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us to delay the filing of our periodic financial reports, which could harm our stock price and, if such delay were to continue for
a period of time, impact our continued listing on the NASDAQ Global Select Market.

We depend on a limited number of suppliers for our products and our business may suffer if we were required to change
suppliers to obtain an adequate supply of components, equipment and raw materials on a timely basis.

Although we generally use parts and components for our products with a high degree of modularity, certain
components are presently available only from a single source or limited sources. We rely on a limited number of suppliers for
the raw materials that are necessary in the production of our consumable medication packages. We have generally been able to
obtain adequate supplies of all components and raw materials in a timely manner from existing sources, or where necessary,
from alternative sources of supply. We engage multiple single source third-party manufacturers to build several of our sub-
assemblies. The risk associated with changing to alternative vendors, if necessary, for any of the numerous components used to
manufacture our products could limit our ability to manufacture our products and harm our business. Due to our reliance on a
few single source partners to build our hardware sub-assemblies and on a limited number of suppliers for the raw materials that
are necessary in the production of our consumable medication packages, a reduction or interruption in supply from our partners
or suppliers, or a significant increase in the price of one or more components could have an adverse impact on our business,
operating results and financial condition. In certain circumstances, the failure of any of our suppliers or us to perform
adequately could result in quality control issues affecting end users' acceptance of our products. These impacts could damage
customer relationships and could harm our business.

The conflict minerals provision of the Dodd-Frank Wall Street Reform and Consumer Protection Act could result in
additional costs and liabilities.

In accordance with the Dodd-Frank Wall Street Reform and Consumer Protection Act, the SEC established new

disclosure and reporting requirements for those companies that use "conflict minerals" mined from the Democratic Republic of
Congo and adjoining countries, whether or not these products are manufactured by third parties. These new requirements could
affect the sourcing of materials used in our products as well as the companies we use to manufacture our products. In
circumstances where conflict minerals in our products are found to be sourced from the Democratic Republic of the Congo or
surrounding countries, we may take actions to change materials or designs to reduce the possibility that our purchase of conflict
minerals may fund armed groups in the region. These actions could add engineering and other costs to the manufacture of our
products.

We expect to incur costs to design and implement a process to discover the origin of the tantalum, tin, tungsten and

gold used in our products, including components we purchase from third parties, and to audit our conflict minerals disclosures.
Our reputation may also suffer if we have included conflict minerals originating in the Democratic Republic of the Congo or
surrounding countries in our products.

Our U.S. government lease agreements are subject to annual budget funding cycles and mandated unilateral changes,
which may affect our ability to enter into such leases or to recognize revenue and sell receivables based on these leases.

U.S. government customers that lease our equipment typically sign contracts with five-year payment terms that are

subject to one-year government budget funding cycles. Further, the government has in certain circumstances mandated
unilateral changes in its Federal Supply Services contract that could render our lease terms with the government less attractive.
In our judgment and based on our history with these accounts, we believe these receivables are collectible. However, in the
future, the failure of any of our U.S. government customers to receive their annual funding, or the government mandating
changes to the Federal Supply Services contract could impair our ability to sell lease equipment to these customers or to sell
our U.S. government receivables to third-party leasing companies. In addition, the ability to collect payments on unsold
receivables could be impaired and may result in a write-down of our unsold receivables from U.S. government customers. The
balance of our unsold leases to U.S. government customers was $12.9 million as of December 31, 2014.

If we fail to manage our inventory properly, our revenue, gross margin and profitability could suffer.

Managing our inventory of components and finished products is a complex task. A number of factors, including, but

not limited to, the need to maintain a significant inventory of certain components that are in short supply or that must be
purchased in bulk to obtain favorable pricing, the general unpredictability of demand for specific products and customer

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requests for quick delivery schedules, may result in us maintaining large amounts of inventory. Other factors, including changes
in market demand, customer requirements and technology, may cause our inventory to become obsolete. Any excess or obsolete
inventory could result in inventory write-downs, which in turn could harm our business and results of operations.

Intellectual property claims against us could harm our competitive position, results of operations and financial condition.

We expect that developers of medication and supply dispensing systems and medication packaging systems, will be

increasingly subject to infringement claims as the number of products and competitors in our industry grows and the
functionality of products in different industry segments overlaps. In the future, third parties may claim that we have infringed
upon their intellectual property rights with respect to current or future products. We do not carry special insurance that covers
intellectual property infringement claims; however, such claims may be covered under our traditional insurance policies. These
policies contain terms, conditions and exclusions that make recovery for intellectual property infringement claims difficult to
guarantee. Any infringement claims, with or without merit, could be time-consuming to defend, result in costly litigation, divert
management's attention and resources, cause product shipment delays or require us to enter into royalty or licensing
agreements. These royalty or licensing agreements, if required, may not be available on terms acceptable to us, or at all, which
could harm our competitive position, results of operations and financial condition.

Our software products are complex and may contain defects, which could harm our reputation, results of operations and
financial condition.

We market products that contain software and products that are software only. Although we perform extensive testing
prior to releasing software products, these products may contain undetected errors or bugs when first released. These may not
be discovered until the product has been used by customers in different application environments. Failure to discover product
deficiencies or bugs could require design modifications to previously shipped products or cause delays in the installation of our
products and unfavorable publicity or negatively impact system shipments, any of which could harm our business, financial
condition and results of operations.

Product liability claims against us could harm our competitive position, results of operations and financial condition.

Our products provide medication management and supply chain management solutions for the healthcare industry.
Despite the presence of healthcare professionals as intermediaries between our products and patients, if our products fail to
provide accurate and timely information or operate as designed, customers, patients or their family members could assert
claims against us for product liability. Moreover, failure of health-care facility employees to use our products for their intended
purposes could result in product liability claims against us. Litigation with respect to product liability claims, regardless of any
outcome, could result in substantial cost to us, divert management's attention from operations and decrease market acceptance
of our products. We possess a variety of insurance policies that include coverage for general commercial liability and
technology errors and omissions liability. We attempt to mitigate these risks through contractual terms negotiated with our
customers. However, these policies and protective contractual terms may not be adequate against product liability claims. A
successful claim brought against us, or any claim or product recall that results in negative publicity about us, could harm our
competitive position, results of operations and financial condition. Also, in the event that any of our products is defective, we
may be required to recall or redesign those products.

We are dependent on technologies provided by third-party vendors, the loss of which could negatively and materially affect
our ability to market, sell, or distribute our products.

Some of our products incorporate technologies owned by third parties that are licensed to us for use, modification, and

distribution. If we lose access to third-party technologies, or we lose the ongoing rights to modify and distribute these
technologies with our products, we will have to devote resources to independently develop, maintain and support the
technologies ourselves, pay increased license costs, or transition to another vendor. Any independent development,
maintenance or support of these technologies by us or the transition to alternative technologies could be costly, time consuming
and could delay our product releases and upgrade schedules. These factors could negatively and materially affect our ability to
market, sell or distribute our products.

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Complications in connection with our ongoing business information system upgrades, including those required to transition
acquired entities onto information systems already utilized, and those implemented to adopt new accounting standards, may
impact our results of operations, financial condition and cash flows.

We continue to upgrade our enterprise-level business information system with new capabilities and transition acquired

entities onto information systems already utilized in the company. In 2014, we replaced legacy Enterprise Requirements
Planning systems utilized in the acquired MTS business with systems currently in use in other parts of Omnicell. In 2015, we
intend to replace the legacy enterprise Requirements Planning systems utilized in Surgichem with systems currently in use in
other parts of Omnicell. Based upon the complexity of some of the upgrades, there is risk that we will not see the expected
benefit from the implementation of these upgrades in accordance with their anticipated timeline and will incur costs in addition
to those we have already planned for. In addition, in future years, we may need to begin efforts to comply with final converged
accounting standards to be established by the Financial Accounting Standards Board ("FASB") and the International
Accounting Standards Board ("IASB") for revenues, leases and other components of our financial reporting. These new
standards could require us to modify our accounting policies. We further anticipate that integration of these and possibly other
new standards may require a substantial amount of management's time and attention and require integration with our enterprise
resource planning system. The implementation of the system and the adoption of future new standards, in isolation as well as
together, could result in operating inefficiencies and financial reporting delays, and could impact our ability to record certain
business transactions timely. All of these potential results could adversely impact our results of operations, financial condition
and cash flows.

Outstanding employee stock options have the potential to dilute stockholder value and cause our stock price to decline.

We grant stock options to certain of our employees as incentives to join Omnicell or as an on-going reward and

retention vehicle. We had options outstanding to purchase approximately 2.7 million shares of our common stock, at a
weighted-average exercise price of $19.02 per share as of December 31, 2014. If some or all of these shares are sold into the
public market over a short time period, the price of our common stock may decline, as the market may not be able to absorb
those shares at the prevailing market prices. Such sales may also make it more difficult for us to sell equity securities in the
future on terms that we deem acceptable.

Changes in our tax rates, the adoption of new tax legislation or exposure to additional tax liabilities could affect our future
results.

We are subject to taxes in the United States and other foreign jurisdictions. Our future effective tax rates could be

affected by several factors, many of which are outside of our control, including: changes in the mix of earnings with differing
statutory tax rates, changes in the valuation of deferred tax assets and liabilities, or changes in tax laws or their interpretation.
We regularly assess the likelihood of adverse outcomes to determine the adequacy of our provision for taxes. We are also
subject to examination of our income tax returns by the Internal Revenue Service and other tax authorities. There can be no
assurance that the outcomes from these examinations will not materially adversely affect our financial condition and operating
results.

Catastrophic events may disrupt our business and harm our operating results.

We rely on our network infrastructure, data centers, enterprise applications, and technology systems for the
development, marketing, support and sales of our products, and for the internal operation of our business. These systems are
susceptible to disruption or failure in the event of a major earthquake, fire, flood, cyber-attack, terrorist attack,
telecommunications failure, or other catastrophic event. Many of these systems are housed or supported in or around our
corporate headquarters located in Northern California, near major earthquake faults, and where a significant portion of our
research and development activities and other critical business operations take place. Other critical systems, including our
manufacturing facilities for our consumable medication packages, are housed in St. Petersburg, Florida in communities that
have been subject to significant tropical storms. Disruptions to or the failure of any of these systems, and the resulting loss of
critical data, which is not quickly recoverable by the effective execution of disaster recovery plans designed to reduce such
disruption, could cause delays in our product development, prevent us from fulfilling our customers' orders, and could severely
affect our ability to conduct normal business operations, the result of which would adversely affect our operating results.

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Anti-takeover provisions in our charter documents and under Delaware law, and any stockholders' rights plan we may
adopt in the future, make an acquisition of us, which may be beneficial to our stockholders, more difficult.

We are incorporated in Delaware. Certain anti-takeover provisions of Delaware law and our charter documents as

currently in effect may make a change in control of our company more difficult, even if a change in control would be beneficial
to the stockholders. Our anti-takeover provisions include provisions in our certificate of incorporation providing that
stockholders' meetings may only be called by our Board of Directors and provisions in our bylaws providing that the
stockholders may not take action by written consent and requiring that stockholders that desire to nominate any person for
election to our Board of Directors or to make any proposal with respect to business to be conducted at a meeting of our
stockholders be submitted in appropriate form to our Secretary within a specified period of time in advance of any such
meeting. Delaware law also prohibits corporations from engaging in a business combination with any holders of 15% or more
of their capital stock until the holder has held the stock for three years unless, among other possibilities, our Board of Directors
approves the transaction. Our Board of Directors may use these provisions to prevent changes in the management and control
of our company. Also, under applicable Delaware law, our board of directors may adopt additional anti-takeover measures in
the future.

The stockholder rights plan adopted by our Board of Directors in February 2003 expired by its terms in February

2013. Our Board of Directors could adopt a similar plan in the future if it determines that such action is in the best interests of
our stockholders. Such a plan may have the effect of discouraging, delaying or preventing a change in control of our company
that may be beneficial to our stockholders.

ITEM 1B. UNRESOLVED STAFF COMMENTS

There are currently no unresolved issues with respect to any Commission staff’s written comments that were received

at least 180 days before the end of our fiscal year to which this report relates and that relate to our periodic or current reports
under the Exchange Act.

ITEM 2. PROPERTIES

Our headquarters is located in leased facilities in Mountain View, California. In addition, we maintain leased office
space in California, Florida, Illinois, Tennessee, and the United Kingdom. The following is a list of our leased facilities and
their primary functions.

Site

Major Activity

Segment

Approximate Square
Footage

St. Petersburg, Florida

Mountain View, California

Administration, marketing, research and
development and manufacturing
Administration, marketing, and research and
development

Milpitas, California

Manufacturing

Waukegan, Illinois

Technical support and training

Nashville, Tennessee

Research and development and marketing

Medication Adherence

132,500

Automation and
Analytics
Automation and
Analytics
Automation and
Analytics
Automation and
Analytics

100,000

46,000

38,000

25,000

Stockport, United
Kingdom (1)

Administration, sales, marketing and
distribution center

Medication Adherence

19,500

Leeds, United Kingdom

Sales, marketing and distribution center

_________________________________________________

Automation and
Analytics
and Medication
Adherence

16,500

(1)

Leased facilities as a result of our acquisition of Surgichem in August 2014.

We also have smaller rented offices in Strongsville, Ohio, the United Arab Emirates, the People's Republic of China,

Hong Kong and the Federal Republic of Germany.

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We believe that these facilities are sufficient for our current operational needs and that suitable additional space will

be available on commercially reasonable terms to accommodate expansion of our operations, if necessary.

For additional information regarding our obligations pursuant to operating leases, see Note 12, Commitments, of the

Notes to Consolidated Financial Statements in this annual report.

ITEM 3. LEGAL PROCEEDINGS

The information set forth under "Legal Proceedings" in Note 13, Contingencies, of the Notes to Consolidated

Financial Statements in this annual report is incorporated herein by reference.

On March 19, 2015, a putative class action lawsuit was filed against the Company and two executive officers in the
U.S. District Court for the Northern District of California, captioned Nelson v. Omnicell, Inc., et al., Case No. 3:15-cv-01280-
HSG. The complaint purports to assert claims on behalf of a class of purchasers of the Company’s stock between May 2, 2014
and March 2, 2015. It alleges that defendants violated Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 by
purportedly making false and misleading statements regarding the existence of a “side letter” arrangement and the adequacy of
internal controls that allegedly resulted in false and misleading financial statements. The Company and the individual
defendants have not yet been served with the Complaint. The Company believes that the claims have no merit and will defend
the lawsuit vigorously.

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 for Our Common Stock

Our common stock is traded on The NASDAQ Global Select Market under the symbol "OMCL." The following table

sets forth the high and low sales prices per share of our common stock for the periods indicated.

Year Ended December 31, 2014

Fourth Quarter
Third Quarter

Second Quarter

First Quarter

Year Ended December 31, 2013

Fourth Quarter
Third Quarter

Second Quarter

First Quarter

Stockholders

High

34.00 $
29.73 $
29.49 $
30.33 $

High

25.89 $
25.22 $
20.88 $
20.00 $

$
$

Low
26.05
26.00
25.00
24.85

Low
20.88
19.29
17.01
14.68

There were 124 registered stockholders of record as of December 31, 2014. A substantially greater number of
stockholders are beneficial holders, whose shares of record are held by banks, brokers and other financial institutions.

Dividend Policy

We have never declared or paid any cash dividends on our common stock. We currently expect to retain any future

earnings for use in the operation and expansion of our business and do not anticipate paying any cash dividends on our common
stock in the foreseeable future.

Performance Graph

The following graph compares total stockholder returns for Omnicell's common stock for the past five years to two

indexes: The NASDAQ Composite Index and the NASDAQ Health Services Index. The graph assumes $100 was invested in
each of the Company’s common stock, the NASDAQ Composite Index, and the NASDAQ Health Services Index as of the
market close on December 31, 2009. The total return for Omnicell's common stock and for each index assumes the
reinvestment of all dividends, although cash dividends have never been declared on Omnicell's common stock, and is based on
the returns of the component companies weighted according to their capitalization as of the end of each annual period.

The NASDAQ Composite Index tracks the aggregate price performance of equity securities traded on The NASDAQ
Stock Market. The NASDAQ Health Services Index tracks the aggregate price performance of health services equity securities.
Omnicell's common stock is traded on The NASDAQ Global Select Market and is a component of both indexes. The stock
price performance shown on the graph is not necessarily indicative of future price performance.

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COMPARISON OF 5 YEAR CUMULATIVE TOTAL RETURN (1)

Among Omnicell, Inc., the NASDAQ Composite Index, and the NASDAQ Health Services Index (2)

_________________________________________________

(1)

(2)

$100 invested on December 31, 2009 in stock or index, including reinvestment of dividends.

This section is not deemed "soliciting material" or to be "filed" with the SEC and is not to be incorporated by reference
into any filing of Omnicell, Inc. under the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934,
as amended, whether made before or after the date hereof and irrespective of any general incorporation language in
any such filing.

Omnicell, Inc.
NASDAQ Composite

NASDAQ Health Services

Stock Repurchase Programs

Year Ended December 31,

2009
100.00
100.00
100.00

2010
123.61
117.61
100.48

2011
141.32
118.70
82.48

2012
127.20
139.00
93.99

2013
218.39
196.83
134.74

2014
283.32
223.74
161.37

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The following table presents a summary of our stock repurchase activity in the fourth quarter of 2014:

Total
Number of
Shares
Purchased (1)

Average
Price
Paid per
Share

Total
Number of
Shares
Purchased
Under
Publicly
Announced
Programs (1)

Maximum Dollar
Value of Shares That
May Yet Be Purchased
Under Plans or
Programs(2)

(In thousands, except per share data)

October 1, 2014 to October 31, 2014

November 1, 2014 to November 30, 2014

December 1, 2014 to December 31, 2014

Total

_________________________________________________

163,196 $

—
—
163,196

27.29
—
—

163,196 $

—
—

163,196 $

54,947
—
—
54,947

(1)

(2)

Shares purchased under the 2012 Stock Repurchase Program.

In August 2012, our Board of Directors authorized a program to repurchase up to $50.0 million of common stock
beginning in 2012, of which approximately $45.1 million has been repurchased as of December 31, 2014. In
November 2014, our Board of Directors authorized a program to repurchase up to $50.0 million of common stock. We
expect to begin repurchasing shares under the 2014 Stock Repurchase Program upon the completion of the 2012 Stock
Repurchase Program. Our stock repurchase programs do not obligate us to acquire any specific number of shares, and
shares may be repurchased in privately negotiated and/or open market transactions, including plans complying with
Rule 10b5-1 of the Exchange Act. Our stock repurchase programs have a total of $54.9 million remaining for future
repurchases as of December 31, 2014, and neither program has an expiration date.

Refer to Note 15, Stock Repurchases, of the Notes to Consolidated Financial Statements in this annual report for

information regarding our authorized Stock Repurchase Programs.

ITEM 6. SELECTED FINANCIAL DATA

The following selected consolidated financial data is derived from our Consolidated Financial Statements. This data

should be read in conjunction with our Consolidated Financial Statements and related Notes included in this annual report and
with Item 7, Management’s Discussion and Analysis of Financial Condition and Results of Operations. Historical results may
not be indicative of future results.

Consolidated Statements of Operations Data:

Total revenue

Gross profit
Income from operations (1)
Net income

Net income per share:

Basic

Diluted

Shares used in per shares calculations:

Basic

Diluted

Cash dividends declared per share

Year Ended December 31,

2014 (2)

2013

2012 (3)

2011

2010 (4)

(In thousands, except per share amounts)

440,900 $
233,860 $
49,583 $
30,518 $

380,585 $
203,399 $
35,299 $
23,979 $

314,027 $
170,588 $
27,126 $
16,178 $

245,535 $
135,784 $
16,222 $
10,389 $

222,407
117,917
9,526
4,892

0.86 $
0.83 $

0.69 $
0.67 $

0.49 $
0.47 $

0.31 $
0.30 $

35,650
36,622

34,736
35,777

33,307
34,213

33,123
34,103

— $

0.15
0.15

32,651
33,513
—

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Consolidated Balance Sheet Data:

Total assets

Total liabilities

$
Total stockholders' equity
__________________________________________________

December 31,

2014 (2)

2013

2012 (3)

2011

2010 (4)

(In thousands)

560,214 $
170,116 $
390,098 $

492,501 $
143,504 $
348,997 $

441,819 $
134,269 $
307,550 $

363,849 $
80,935 $
282,914 $

343,224
78,010
265,214

(1)

Income from operations includes the following items:

Share-based compensation expense

12,785 $

11,151 $

9,214 $

9,499 $

9,015

2014 (2)

2013

2012 (3)

2011

2010 (4)

Year Ended December 31,

(In thousands)

(2)
(3)
(4)

Includes Surgichem results as of August 2014.
Includes MTS results as of May 2012.
Includes Pandora results as of September 2010.

SUPPLEMENTARY CONSOLIDATED FINANCIAL DATA

2014 Consolidated Statements of Operations Data:

December 31, 2014 September 30, 2014 (2)

June 30, 2014

March 31, 2014

Quarter Ended

(In thousands, except per share data)
(Unaudited)

Total revenue

Gross profit

Income from operations

Net income

Net income per share:
Basic (1)
Diluted (1)

121,541 $
63,779
13,474
9,235 $

0.26 $
0.25 $

112,543 $
59,546
13,597
7,300 $

105,052 $
56,040
12,558
7,789 $

0.20 $
0.20 $

0.22 $
0.21 $

Quarter Ended

101,764
54,495
9,954
6,194

0.18
0.17

December 31, 2013

September 30, 2013

June 30, 2013

March 31, 2013

(In thousands, except per share data)
(Unaudited)

2013 Consolidated Statements of Operations Data:
Total revenue

Gross profit

Income from operations

Net income

Net income per share:
Basic (1)
Diluted (1)

105,750 $
56,624
11,055
6,823 $

0.19 $
0.19 $

94,039 $
52,040
10,717
7,755 $

0.22 $
0.21 $

93,686 $
49,368
9,359
6,016 $

0.17 $
0.17 $

87,110
45,367
4,169
3,385

0.10
0.10

_________________________________________________

(1)

Quarterly net income per share figures may not total to annual net income per share, due to rounding and immaterial
fluctuations in the number of options included or omitted from diluted calculations based on the stock price or option
exercise prices and/or net losses recorded in quarterly periods.

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(2)

Includes Surgichem results as of August 2014.

ITEM 7. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF
OPERATIONS

The following discussion and analysis should be read in conjunction with our Consolidated Financial Statements and

related notes in this annual report. This discussion may contain forward-looking statements based upon current expectations
that involve risks and uncertainties. Our actual results and the timing of selected events could differ materially from those
anticipated in these forward-looking statements as a result of several factors, including those set forth under Item 1A "Risk
Factors" and elsewhere in this annual report. Unless otherwise stated, references in this report to particular years or quarters
refer to our fiscal year and the associated quarters of those fiscal years.

Our Business

OVERVIEW

We are a leading provider of comprehensive automation and business analytics software solutions for patient-centric
medication and supply management across the entire healthcare continuum, from the acute care hospital setting to post-acute
skilled nursing and long-term care facilities to the home. Our Omnicell Automation and Analytic customers worldwide utilize
our medication automation, supply chain and analytics solutions to help enable them to increase operational efficiency, reduce
errors, deliver actionable intelligence and improve patient safety.

Omnicell Medication Adherence solutions, including the MTS and Surgichem brands, provide innovative medication
adherence packaging solutions that can help reduce costly hospital readmissions and enable institutional and retail pharmacies
worldwide to maintain high accuracy and quality standards in medication dispensing and administration while optimizing
productivity and controlling costs.

We sell our product and consumable solutions together with related service offerings. Revenue generated in the United

States represented 89% of our total revenues in 2014 and we expect our revenues from international operations to increase in
future periods as we continue to grow our international business. We have not sold in the past, and have no future plans to sell
our products either directly or indirectly, to customers located in countries that are identified as state sponsors of terrorism by
the U.S. Department of State, and are subject to economic sanctions and export controls.

Operating Segments

In the first quarter of 2014, we began to manage our business according to two product segments as many of our Acute

Care and Non-Acute Care customers are converging to provide services across the continuum of care. These customers seek
Automation and Analytics products that function across the various facilities they manage, and we find ourselves providing
solutions across multiple types of care environments. These customers are also interested in obtaining higher levels of
adherence to prescribed medication regimens that our blister card products can help provide. Our business has evolved to be
managed more on a product basis and it has become more difficult to determine whether a customer is a hospital or a blend of
hospitals and non-acute care facilities.

We modified our segment reporting structure to match our new operating structure in the first quarter of 2014. The two
operating segments which are the same as our reporting segments are Automation and Analytics and Medication Adherence. As
our business evolves, we will continue to assess our operating units which could result in future modifications to our current
operating segments. For further description of our operating segments, Note 17, Segment Information, of the Notes to
Consolidated Financial Statements in this annual report.

Strategy

The healthcare market is experiencing a period of substantive change. The adoption of electronic healthcare records,
new regulatory constraints, and changes in the reimbursement structure have caused healthcare institutions to re-examine their
operating structures, re-prioritize their investments, and seek efficiencies. We believe our customers’ evolving operating
environment creates challenges for any supplier, but also affords opportunities for suppliers that are able to partner with
customers to help them meet the changing demands. We have and intend to continue to invest in the strategies which we

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believe have generated and will continue to generate our revenue and earnings growth, while supporting our customers’
initiatives and needs. These strategies include:

• Development of differentiated products. We invest in the development of products that we believe bring patient
safety and workflow efficiency to our customers’ operations that they cannot get from other competing solutions.
These differentiators may be as small as how a transaction operates or information provided on a report or as large
as the entire automation of a workflow that would otherwise be completed manually. We intend to continue our
focus on differentiating our products, and we carefully assess our investments regularly as we strive to ensure
those investments provide the solutions most valuable to our customers.

• Deliver our solutions to new markets. Areas of healthcare where work is done manually may benefit from our

existing solutions. These areas include hospitals that continue to utilize manual operations, healthcare segments of
the U.S. market outside hospitals and markets outside the United States. We weigh the cost of entering these new
markets against the expected benefits and focus on the markets that we believe are most likely to adopt our
products.

• Expansion of our solutions through acquisitions and partnerships. Our acquisitions have generally been
focused on automation of manual workflows or data analytics, which is the enhancement of data for our
customers’ decision-making processes. We believe that expansion of our product lines through acquisition and
partnerships to meet our customers changing and evolving expectations is a key component to our historical and
future success.

Our investments have been consistent with the strategies outlined above. To differentiate our solutions from others

available in the market, we began shipping a refresh of our product line in 2011, which we market as G4. The G4 refresh
included multiple new products and an upgrade product that allowed existing customers to augment their installations to obtain
the most current technology that we provide. The G4 product refresh has been a key contributor to our growth, with 61% of our
automation and analytics installed base ordering upgrades to their existing systems since the announcement of G4. In addition
to enhanced capabilities, we have focused on attaining the highest quality and service measurements for G4 in the industry,
while marketing the solution to new and existing customers. Our research and development efforts today are designed to bring
new products to market beyond the G4 product line that we believe will meet customer needs in years to come.

Consistent with our strategy to enter new markets, we have made investments in our selling, general and

administrative expenses to expand our sales team and market to new customers. Our international efforts have focused
primarily on four markets: the United Kingdom where we sell medication adherence products through a direct sales team and
automation and analytics products through a distributor, Germany where we sell medication adherence products through a
direct sales team, Middle Eastern countries of the Arabian Peninsula where new healthcare facility construction is taking place,
and in China, where we launched a Mandarin version of our automated dispensing systems in 2011. In the third quarter of
2012, we purchased 15% of our United Kingdom automation and analytics products distributor’s outstanding equity for
approximately $0.9 million in cash to accelerate the adoption of medication and supply automation. In connection with the
investment, we have the right, under certain circumstances, to appoint a member to this company's board of directors as well as
certain other voting rights and, therefore, we believe we have the ability to exert significant influence over this distributor's
operations. Our proportionate equity share of the income of this distributor, recognized in interest and other income, net, was
immaterial for the years ended December 31, 2014, December 31, 2013 and December 31, 2012. We have also expanded our
sales efforts to medication adherence customers in the United States which has allowed us to sell our automated dispensing
solutions and other products to this market.

Expansion of our solutions through acquisitions and partnerships include our acquisition of MTS in 2012 and our

acquisition of Surgichem in August 2014. Surgichem is a provider of medication adherence products in the United Kingdom.
We have also developed relationships with major providers of hospital information management systems with the goal of
enhancing the interoperability of our products with their systems. We believe that enhanced interoperability will help reduce
implementation costs, time, and maintenance for shared clients, while providing new clinical workflows designed to enhance
efficiency and patient safety.

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We believe that the success of our three leg strategy of differentiated products, expansion into new markets, and

acquisition and partnership in future periods will be based on, among other factors:

• Our expectation that the overall market demand for healthcare services will increase as the population grows, life

expectancies continue to increase and the quality and availability of healthcare services increases;

• Our expectation that the environment of increased patient safety awareness, increased regulatory control,

increased demand for innovative products that improve the care experience and increased need for workflow
efficiency through the adoption of technology in the healthcare industry will make our solutions a priority in the
capital budgets of healthcare facilities; and

• Our belief that healthcare customers will continue to value a consultative customer experience from their

suppliers.

Among other financial measures, we utilize product bookings to assess the current success of our strategies. Product

bookings consist of all firm orders, as evidenced by a contract and purchase order for equipment and software, and by a
purchase order for consumables. Equipment and software bookings are installable within twelve months and generally recorded
as revenue upon customer acceptance of the installation. Consumables are recorded as revenue upon shipment to a customer or
receipt by the customer, depending upon contract terms. Consumable bookings are generally recorded as revenue within one
month. Product bookings increased 11%, from $327.8 million in 2013 to $364.0 million in 2014, driven by the success of our
growth strategies in differentiated products and new markets and, to a lesser extent, by the partial year of contribution from the
acquisition of Surgichem.

In addition to product solution sales, we provide services to our customers. Our healthcare customers expect a high

degree of partnership involvement from their technology suppliers throughout their ownership of the products. We provide
extensive installation planning and consulting as part of every product sale and included in the initial price of the solution. Our
customers' medication control systems are mission critical to their success and our customers require these systems to be
functional at all times. To help assure the maximum availability of our systems, our customers typically purchase maintenance
and support contracts in one, two or five year increments. As a result of the growth of our installed base of customers, our
service revenues have also grown. We strive to provide the best service possible, as measured by third-party rating agencies and
by our own surveys, to assure our customers continue to seek service maintenance from us. Our liabilities include current and
long-term deferred service revenue of $45.5 million and $40.4 million as of December 31, 2014 and December 31, 2013,
respectively. Our deferred service revenue will be amortized to service revenue as the service contracts are executed.

The growth in our Automation and Analytics revenue was driven primarily by our success in consistently growing the
number of our customer installations for the year ended December 31, 2014. Installed customers in the United States grew from
1,806 hospitals as of December 31, 2013 to 1,935 hospitals as of December 31, 2014. To a lesser extent, but of equal
importance, revenue growth was also driven by our success in upgrading installed customers to newer G4 technology, which is
in line with our strategy of striving to deliver differentiated innovation in our solutions. Our larger installed base has provided
growth opportunities and, as a result, our service revenues have also grown for the year ended December 31, 2014.

The growth in our Medication Adherence revenue was driven primarily by increased sales of our OnDemand

medication packaging systems in the United States market and increased adoption of multi-medication adherence solutions
used by patients in assisted living or home care in Europe for the year ended December 31, 2014. This growth is in line with
our strategy to deliver solutions to markets outside the United States. On a geographic basis, the United States market did not
contribute to, nor erode, the growth in our Medication Adherence business as the population of patients living in nursing homes
in the United States has remained relatively constant over the past year.

In the future, we expect our strategies to evolve as the business environment of our customers evolves, but for our

focus to remain on improving healthcare with solutions that help change the practices in ways that improve patient and provider
outcomes. We expect our investment in differentiated products, new markets, and acquisitions and partnerships to continue. In
2015, we also intend to manage our business to operating profit margins similar to those achieved in 2014. Our full-time
headcount of 1,236 on December 31, 2014, which is an increase of 102 from December 31, 2013, is dedicated to bringing our
strategies to bear in all the markets we participate in.

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CRITICAL ACCOUNTING POLICIES AND ESTIMATES

Our discussion and analysis of our financial condition and results of operations are based on our Consolidated

Financial Statements, which have been prepared in accordance with United States Generally Accepted Accounting Principles
("U.S. GAAP"). The preparation of these financial statements requires us to make certain estimates and assumptions that affect
the reported amounts of assets and liabilities, disclosure of any contingent assets and liabilities at the date of the financial
statements and the reported amounts of revenues and expenses during the reporting periods. We regularly review our estimates
and assumptions, which are based on historical experience and various other factors that are believed to be reasonable under the
circumstances, the results of which form the basis for making judgments about the carrying values of certain assets and
liabilities that are not readily apparent from other sources. Actual results may differ from these estimates and assumptions. We
believe the following critical accounting policies are affected by significant judgments and estimates used in the preparation of
our Consolidated Financial Statements:

Revenue recognition

We earn revenues from sales of our medication and medical and surgical supply automation systems along with
consumables and related services that are sold in the healthcare industry, our principal market. Revenues related to consumable
products are reported net of discounts provided to our customers. Our customer arrangements typically include one or more of
the following deliverables:

Products. Software-enabled equipment that manages and regulates the storage and dispensing of pharmaceuticals,

consumable blister cards and packaging equipment and other medical supplies.

Software. Additional software applications that enable incremental functionality of our equipment.

Installation. Installation of equipment as integrated systems at customers' sites.

Post-installation technical support. Phone support, on-site service, parts and access to unspecified software upgrades

and enhancements, if and when available.

Professional services. Other customer services, such as training and consulting.

We recognize revenue when the earnings process is complete, based upon our evaluation of whether the following four

criteria have been met:

Persuasive evidence of an arrangement exists. We use signed customer contracts and signed customer purchase orders

as evidence of an arrangement for leases and sales. For service engagements, we use a signed services agreement and a
statement of work to evidence an arrangement.

Delivery has occurred. Equipment and embedded software product delivery is deemed to occur upon successful
installation and receipt of a signed and dated customer confirmation of installation letter, providing evidence that we have
delivered what a customer ordered. In instances of a customer self-installation, product delivery is deemed to have occurred
upon receipt of a signed and dated customer confirmation letter. If a sale does not require installation, we recognize revenue on
delivery of products to the customer, including transfer of title and risk of loss, assuming all other revenue criteria are met. For
existing distributors, where installation of equipment training has been previously provided and the distributor is certified to
install our equipment at the end-user customer facility, we recognize revenue from sales of products to the distributor upon
shipment assuming all other revenue criteria are met, since we do not allow for rights of return or refund. For new distributors,
where we have not provided installation of equipment training, revenue on the sales of products to the distributor is deferred
until the distributor has completed the Distributor Training Program and has been certified to install our equipment at the end-
user facility. For the sale of consumable blister cards, we recognize revenue when title and risk of loss of the products shipped
have transferred to the customer, which usually occurs upon shipment from our facilities. Assuming all other revenue criteria
are met, we recognize revenue for support services ratably over the related support services contract period. We recognize
revenue on training and professional services as they are performed.

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Fee is fixed or determinable. We assess whether a fee is fixed or determinable at the outset of the arrangement based

on the payment terms associated with the transaction. We have established a history of collecting under the original contract
without providing concessions on payments, products or services.

Collection is probable. We assess the probability of collecting from each customer at the outset of the arrangement
based on a number of factors, including the customer's payment history and its current creditworthiness. If, in our judgment,
collection of a fee is not probable, we defer the revenue until the uncertainty is removed, which generally means revenue is
recognized upon our receipt of cash payment assuming all other revenue criteria are met. Our historical experience has been
that collection from our customers is generally probable.

In arrangements with multiple deliverables, assuming all other revenue criteria are met, we recognize revenue for

individual delivered items if they have value to the customer on a standalone basis. We allocate arrangement consideration at
the inception of the arrangement to all deliverables using the relative selling price method. This method requires us to
determine the selling price at which each deliverable could be sold if it were sold regularly on a standalone basis. When
available, we use vendor-specific objective evidence ("VSOE") of the selling price. VSOE represents the price charged for a
deliverable when it is sold separately, or for a deliverable not yet being sold separately, the price established by management
with the relevant authority. We consider VSOE to exist when approximately 80% or more of our standalone sales of an item are
priced within a reasonably narrow pricing range (plus or minus 15% of the median rates). We have established VSOE of the
selling price for our post-installation technical support services and professional services. When VSOE of selling price is not
available, third-party evidence ("TPE") of selling price for similar products and services is acceptable; however, our offerings
and market strategy differ from those of our competitors, such that we cannot obtain sufficient comparable information about
third parties' prices. If neither VSOE nor TPE are available, we use our best estimates of selling prices ("BESP"). We determine
BESP considering factors such as market conditions, sales channels, internal costs and product margin objectives and pricing
practices. We regularly review and update our VSOE and BESP information.

The relative selling price method allocates total arrangement consideration proportionally to each deliverable (an

"Element") on the basis of its estimated selling price. In addition, the amount recognized for any delivered Elements cannot
exceed that which is contingent upon delivery of any remaining Elements in the arrangement.

We also use the residual method to allocate revenue between the software products that enable incremental equipment
functionality, and thus are not deemed to deliver its essential functionality, and the related post-installation technical support, as
these products and services continue to be accounted for under software revenue recognition rules. Under the residual method,
the amount allocated to the undelivered elements equals VSOE of fair value of these elements. Any remaining amounts are
attributed to the delivered items and are recognized when those items are delivered.

A portion of our sales are made through multi-year lease agreements. Under sales-type leases, we recognize revenue

for our hardware and software products net of lease execution costs such as post-installation product maintenance and technical
support, at the net present value of the lease payment stream once our installation obligations have been met. We optimize cash
flows by selling a majority of our non-U.S. government leases to third-party leasing finance companies on a non-recourse basis.
We have no obligation to the leasing company once the lease has been sold. Some of our sales-type leases, mostly those
relating to U.S. government hospitals, are retained in-house. Interest income on these leases is recognized as a component of
product revenue using the interest method.

Accounts receivable and notes receivable (net investment in sales-type leases)

We actively manage our accounts receivable to minimize credit risk. We typically sell our products to customers for

which there is a history of successful collection. New customers are subject to a credit review process, which evaluates that
customer's financial position and ability to pay. We continually monitor and evaluate the collectability of our trade receivables
based on a combination of factors. We record specific allowances for doubtful accounts when we become aware of a specific
customer's impaired ability to meet its financial obligation to us, such as in the case of bankruptcy filings or deterioration of
financial position.

Uncollectible amounts are charged off against trade receivables and the allowance for doubtful accounts when we

make a final determination that there is no reasonable expectation of recovery. Estimates are used in determining our

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allowances for all other customers based on factors such as current trends, the length of time the receivables are past due and
historical collection experience. While we believe that our allowance for doubtful accounts receivable is adequate and that the
judgment applied is appropriate, such estimated amounts could differ materially from what will actually be uncollectible in the
future.

The retained in-house leases discussed above are considered financing receivables. Our credit policies and evaluation
of credit risk and write-off policies are applied alike to trade receivables and the net investment in sales-type leases. For both,
an account is generally past due after thirty days. The financing receivables also have customer-specific reserves for accounts
identified for specific impairment and a non-specific reserve applied to the remaining population, based on factors such as
current trends, the length of time the receivables are past due and historical collection experience. The retained in-house leases
are not stratified by portfolio or class. Financing receivables which are reserved are generally transferred to cash-basis
accounting so that revenue is recognized only as cash is received. However, the cash basis accounts continue to accrue interest.

Valuation and impairment of goodwill, intangible assets and other long-lived assets

Business combination valuations. When we acquire businesses, we allocate the purchase price to tangible assets and

liabilities and identifiable intangible assets acquired. Any residual purchase price is recorded as goodwill. The allocation of the
purchase price requires management to make significant estimates in determining the fair values of assets acquired and
liabilities assumed, especially with respect to intangible assets. These estimates are based on information obtained from
management of the acquired companies and historical experience. These estimates can include, but are not limited to:

•

cash flows that an asset is expected to generate in the future;

the acquired company’s brand and competitive position, as well as assumptions about the period of time the
acquired brand will continue to be used in the combined company’s product portfolio;

•

cost savings expected to be derived from acquiring an asset; and

• discount rates.

These estimates are inherently uncertain and unpredictable, and if different estimates were used, the purchase price for

the acquisition could be allocated to the acquired assets and liabilities differently from the allocation that we have made. In
addition, unanticipated events and circumstances may occur which may affect the accuracy or validity of such estimates, and if
such events occur we may be required to record a charge against the value ascribed to an acquired asset or an increase in the
amounts recorded for assumed liabilities.

Goodwill impairment. We review goodwill for impairment on an annual basis on the first day of the fourth quarter of

each year at the reporting unit level. Our reporting units are the same as our operating segments, which are Automation and
Analytics and Medication Adherence. A qualitative assessment is initially made to determine whether it is necessary to perform
quantitative testing. This initial assessment includes, among others, consideration of: (i) past, current and projected future
earnings and equity; (ii) recent trends and market conditions; and (iii) valuation metrics involving similar companies that are
publicly-traded and acquisitions of similar companies, if available. If this initial qualitative assessment indicates that it is more
likely than not that impairment exists, or if we decide to bypass this option, we proceed to a two-step impairment test. The first
step ("Step 1") involves a comparison between the estimated fair values of our reporting units with their respective carrying
amounts including goodwill. The methods for estimating reporting unit values include asset and liability fair values and other
valuation techniques, such as discounted cash flows and multiples of earnings or revenues. If the carrying value exceeds
estimated fair value, there is an indication of potential impairment, and the second step is performed to measure the amount of
impairment. The second step involves calculating an implied fair value of goodwill by measuring the excess of the estimated
fair value of the reporting units over the aggregate estimated fair values of the individual assets less liabilities. If the carrying
value of goodwill exceeds the implied fair value of goodwill, an impairment charge is recorded for the excess.

The process of estimating the fair value and carrying value of our reporting units’ equity requires significant judgment

at many points during the analysis. Various assets and liabilities are not specifically allocated to an individual reporting unit,
and therefore, we apply judgment to allocate the assets and liabilities, and this allocation affects the carrying value of the
respective reporting units. Applying the income approach requires that we make a number of important estimates and

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assumptions. We estimate the future cash flows of each reporting unit based on historical and forecasted revenue and operating
costs. This involves further estimates, such as estimates of future revenue and expense growth rates. In addition, we apply a
discount rate to the estimated future cash flows for the purpose of the valuation. This discount rate is based on the estimated
weighted-average cost of capital for each reporting unit and may change from year to year. Changes in these key estimates and
assumptions, or in other assumptions used in this process, could materially affect our impairment analysis for a given year.

Based on a Step 1 impairment analysis performed as of October 1, 2014, we determined that it was more likely than

not that the fair value of each of our reporting units exceeded the carrying value by approximately 25%, and thus no
impairment in our reporting units.

Intangible assets and other long-lived assets. We assess the impairment of identifiable intangible assets and other

long-lived assets whenever events or changes in circumstances indicate that an asset's carrying amount may not be recoverable.
Recoverability of an asset is measured by the comparison of the carrying amount to the sum of the undiscounted estimated
future cash flows the asset is expected to generate, offset by estimated future costs to dispose of the product to which the asset
relates. If an asset is considered to be impaired, the amount of such impairment would be measured as the difference between
the carrying amount of the asset and its fair value. Our cash flow assumptions are based on historical and forecasted future
revenue, operating costs, and other relevant factors. Assumptions and estimates about the remaining useful lives of our
intangible assets and other long-lived assets are subjective and are affected by changes to our business strategies. If
management’s estimates of future operating results change, or if there are changes to other assumptions, the estimate of the fair
value of our assets could change significantly. Such change could result in impairment charges in future periods, which could
have a significant impact on our operating results and financial condition.

Inventory

Inventories are stated at the lower of cost (utilizing standard costs), applying the first-in, first-out method, or market.
We routinely assess our on-hand inventory for timely identification and measurement of obsolete, slow-moving or otherwise
impaired inventory. We write down inventory for estimated obsolescence, excess or unmarketable quantities equal to the
difference between the cost of the inventory and its estimated market value based on assumptions about future demand and
market conditions, or lower of cost or market. If actual future demand or market conditions are less favorable than we
projected, additional inventory write-downs may be required.

Valuation of share-based awards

We account for share-based compensation in accordance with ASC 718, Stock Compensation ("ASC 718"). We
recognize compensation expense related to stock-compensation, including the awarding of employee stock options and
restricted stock units, based on the grant date estimated fair value. We amortize the fair value of the employee stock options on
a straight-line basis over the requisite service period of the award, which is generally the vesting period. We estimate the fair
value of stock-based compensation awards using the Black-Scholes option pricing model, which requires the following inputs:
expected life, expected volatility, risk-free interest rate, expected dividend yield rate, exercise price, and closing price of our
common stock on the date of grant. The expected volatility is based on a combination of historical and market-based implied
volatility, and the expected life of the awards is based on our historical experience of employee stock option exercises,
including forfeitures. The valuation assumptions we use in estimating the fair value of employee share-based awards may
change in future periods. We calculate our pool of excess tax benefits available within additional paid-in capital in accordance
with the provisions of ASC 718.

Accounting for income taxes

We record an income tax provision for the anticipated tax consequences of the reported results of operations. In

accordance with ASC 740, Income Taxes ("ASC 740"), the provision for income taxes is computed using the asset and liability
method, which requires the recognition of deferred tax assets and liabilities for the expected future tax consequences of events
that have been included in the financial statements. Under this method, deferred tax assets and liabilities are determined on the
basis of the differences between the financial statement and tax bases of assets and liabilities, and for operating losses and tax
credit carry forwards. Deferred tax assets and liabilities are measured using the enacted tax rates in effect for the periods in
which those tax assets and liabilities are expected to be realized or settled. In the event that these tax rates change, we will incur
a benefit or detriment on our income tax expense in the period of change. If we were to determine that all or part of the net

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deferred tax assets are not realizable in the future, we will record a valuation allowance that would be charged to earnings in the
period such determination is made.

In accordance with ASC 740, we recognize the tax benefit from an uncertain tax position if it is more likely than not
that the tax position will be sustained on examination by the taxing authorities, based on the technical merits of the position.
The tax benefits recognized in the financial statements from such positions are then measured based on the largest benefit that
has a greater than 50% likelihood of being realized upon ultimate settlement. The calculation of tax liabilities involves
significant judgment in estimating the impact of uncertainties in the application of ASC 740 and complex tax laws. Resolution
of these uncertainties in a manner inconsistent with management’s expectations could have a material impact on our financial
condition and operating results.

Recently issued authoritative guidance

Refer to Note 1, Summary of Significant Accounting Policies, of the Notes to Consolidated Financial Statements in

this annual report for a description of recently issued accounting pronouncements, including the expected dates of adoption and
estimated effects on our results of operations, financial positions and cash flows.

Total Revenues

RESULTS OF OPERATIONS

Change in

2014

2013

2012

(Dollars in thousands)

Product revenues

$ 360,344

$ 53,155

17 % $ 307,189

$ 59,535

24 % $ 247,654

Percentage of total revenues

82 %

81 %

79 %

Service and other revenues

80,556

7,160

10 %

73,396

7,023

11 %

66,373

Percentage of total revenues

18 %

19 %

21 %

Total revenues

$ 440,900

$ 60,315

16 % $ 380,585

$ 66,558

21 % $ 314,027

2014 compared to 2013:

Product revenues represented 82%, 81% and 79% of total revenues for the years ended 2014, 2013 and 2012,
respectively. Product revenues increased due to increased sales for both our Automation and Analytics segment of $44.0 million
and Medication Adherence segment of $9.1 million. Service and other revenues represented 18%, 19% and 21% of total
revenues for the years ended 2014, 2013 and 2012, respectively. Service and other revenues include revenues from service and
maintenance contracts and rentals of automation systems. Service and other revenues primarily increased due to an increase
from our Automation and Analytics segment of $7.1 million.

Our international sales represented 11%, 12% and 8% of total revenues for the years ended 2014, 2013 and 2012,
respectively, and are expected to be affected by foreign currency exchange rates fluctuations. We are unable to predict the
extent to which revenue in future periods will be impacted by changes in foreign currency exchange rates.

We anticipate our revenues will continue to increase in 2015 compared to 2014, as we fulfill our existing orders, and

based on our growth in bookings in 2014, some of which will be recognized as revenue in 2015. Our ability to continue to grow
revenue is dependent on our ability to continue to obtain orders from customers, our ability to produce quality consumables to
fulfill customer demand, the volume of installations we are able to complete, our ability to meet customer needs by providing a
quality installation experience, and our flexibility in manpower allocations among customers to complete installations on a
timely basis. The timing of our product revenues for equipment is primarily dependent on when our customers’ schedules allow
for installations.

2013 compared to 2012:

Product revenues increased due to increased sales for both Automation and Analytics segment of $35.3 million and

Medication Adherence segment of $24.2 million, of which $29.2 million was from our MTS operations. Service and other

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revenues increased primarily as a result of an expansion in our installed base of automation systems and a resulting increase in
the number of support service contracts within our Automation and Analytics segment.

Financial Information by Segment

Revenues

Revenues:

Change in

2014

2013

2012

(Dollars in thousands)

Automation and Analytics

$ 354,095

$ 51,178

17 % $ 302,917

$ 42,757

16 % $ 260,160

Percentage of total revenues

80 %

83 %

Medication Adherence

86,805

9,137

12 %

77,668

23,801

44 %

53,867

Percentage of total revenues

20 %

17 %

Total revenues

$ 440,900

$ 60,315

16 % $ 380,585

$ 66,558

21 % $ 314,027

2014 compared to 2013:

Automation and Analytics revenues increased due to an increase in product revenues of $44.0 million primarily due to

the increase of $40.3 million in Medical Automation Cabinets sales and of $7.4 million in Supply Cabinets and Supply
Management software sales, partially offset by a decrease of $3.7 million in revenue related to our leasing business. Service
and other revenues increased by $7.1 million due to higher service renewal fees driven primarily by an increase in installed
base customers and new customers.

Medication Adherence revenues increased due to an increase in product revenues of $9.1 million primarily as a result
of an increase in sales of OnDemand medication packaging systems in the United States and an increase in the adoption of our
multi-medication consumable products by patients in Europe, and includes $4.6 million in revenue from our Surgichem
operations since its acquisition in August 2014. Service and other revenues remained relatively flat compared to the prior year.

2013 compared to 2012:

Automation and Analytics revenues increased due to an increase in product revenues of $35.3 million primarily as a

result of increased customers' receptivity to our products due to product differentiation and entrance into new markets, coupled
with an increase in service revenues of $7.4 million due to an increase in the number of support service contracts as a result of
the expansion in our installed base customers.

Increased Medication Adherence revenues were primarily driven by an increase of $29.2 million in product revenues
related to the MTS acquisition in May of 2012, partially offset by a slight decline in other product revenues. Service and other
revenues remained relatively flat compared to the prior year.

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Cost of revenues and Gross profit

Change in

2014

2013

2012

Cost of revenues:

Automation and Analytics

$ 151,327

$ 22,013

17 % $ 129,314

$ 17,715

16 % $ 111,599

(Dollars in thousands)

As a percentage of related revenues

43 %

Medication Adherence

55,713

7,841

16 %

47,872

16,032

50 %

31,840

As a percentage of related revenues

64 %

62 %

59 %

Total cost of revenues

$ 207,040

$ 29,854

17 % $ 177,186

$ 33,747

24 % $ 143,439

As a percentage of total revenues

47 %

46 %

Gross profit:

Automation and Analytics

Automation and Analytics gross
margin

Medication Adherence

$ 29,165

202,76
8
57 %

17 % $ 173,603

$ 25,042

17 % $ 148,561

57 %

31,092

1,296

4 %

29,796

7,769

35 %

22,027

Medication Adherence gross margin

36 %

38 %

41 %

Total gross profit

Total gross margin

$ 233,860

$ 30,461

15 % $ 203,399

$ 32,811

19 % $ 170,588

53 %

54 %

2014 compared to 2013:

Cost of revenues is primarily comprised of three general categories: (i) standard product costs which accounts for the
majority of the product cost of revenues that are provided to customers, and are inclusive of purchased material, labor to build
the product and overhead costs associated with production; (ii) installation costs as we install our equipment at the customer
site, and include costs of the field installation personnel, including labor, travel expense, and other expenses; and (iii) other
costs including variances in standard costs and overhead, scrap costs, rework, warranty, provisions for excess and obsolete
inventory and amortization of software development costs.

Automation and Analytics

Cost of revenues increased due to an increase in product costs of $20.8 million as a result of an increase of $16.4
million attributed to a different mixture of customers, products and overall growth in product sales, and an increase of $2.9
million in product installation costs. Cost of service revenues increased by $1.2 million due to an increase in salaries and wages
as support headcount increased, in addition to an increase in expenses related to the refurbishment of returned materials.

Gross profit increased due to an increase in product and service revenues while gross margin remained consistent as

cost of sales as a percentage of revenues remained consistent with the prior year.

Medication Adherence

Cost of revenues increased due to an increase in product costs of $7.6 million primarily driven by an increase in

product sales and the inclusion of costs from our Surgichem operations. Consistent with the related revenues, cost of service
sales remained relatively flat compared to the prior year.

Gross profit increased due to an increase in product revenues and the inclusion of Surgichem operations, and gross

margin slightly decreased as cost of sales as a percentage of revenues slightly increased driven by higher product costs.

We do not anticipate any significant fluctuations in gross profit and gross margin beyond normal fluctuations caused

by changes in product mix for our Automation and Analytics and Medication Adherence segments during 2015.

2013 compared to 2012:

Automation and Analytics

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Cost of revenues increased due to an increase in product costs of $17.8 million as a result of increased revenues and

unfavorable changes in product mix. Cost of service sales remained relatively flat compared to the prior year.

Gross profit increased due to an increase in product and service revenues while gross margin remained consistent as

cost of sales as a percentage of revenues remained overall consistent with the prior year.

Medication Adherence

Cost of revenues increased due to an increase in product costs of $14.9 million and service costs of $1.2 million

primarily driven by an increase in product sales and the inclusion of costs from our MTS operations.

Gross profit increased due to an increase in product revenues and the inclusion of MTS operations, and gross margin

slightly decreased as cost of sales as a percentage of revenues slightly increased driven primarily by higher product costs.

Operating expenses and Income from operations

Change in

2014

2013

2012

Operating expenses:

(Dollars in thousands)

Research and development

$ 27,802

$ (1,303 )

(4 )% $ 29,105

$ 5,379

23 % $ 23,726

As a percentage of total revenues

6 %

8 %

Selling, general and administrative 156,475

17,480

13 % 138,995

19,259

16 % 119,736

As a percentage of total revenues

35 %

37 %

38 %

Total operating expenses

$ 184,277

$ 16,177

10 % $ 168,100

$ 24,638

17 % $ 143,462

As a percentage of total revenues

42 %

44 %

46 %

Income from operations:

Automation and Analytics

$ 47,612

$ 14,096

42 % $ 33,516

$ 12,422

59 % $ 21,094

Operating margin

Medication Adherence

Operating margin

13 %

1,971

2 %

188

11 %

1,783

(4,249 )

(70 )%

11 %

2 %

8 %

6,032

11 %

Total income from operations

$ 49,583

$ 14,284

40 % $ 35,299

$ 8,173

30 % $ 27,126

Total operating margin

11 %

9 %

2014 compared to 2013:

Research and development expenses decreased in our Automation and Analytics and Medication Adherence segments,

primarily due to an increase of $3.2 million in the capitalization of software development costs in 2014 compared to 2013,
partially offset by increased expenses of $2.7 million to further enhance our Pharmacy and Supply automation products. In our
Medication Adherence segment, research and development decreased primarily due to the write-off of $1.8 million of
capitalized software development costs in 2013 which did not recur in 2014, partially offset by an increase of $1.0 million in
expenses to bring new medication adherence products to market, such as our M5000 packaging system.

We expect research and development expenses to increase in 2015 as we continue to invest in new products and

services, and increase as a percentage of total revenues from 6% to approximately 8%. The amount of research and
development expenses can fluctuate based on the amount of prototype expenses for hardware and/or the amount of capitalized
software development costs.

Selling, general and administrative expenses increased due to increases from our Automation and Analytics segment of

$15.6 million and Medication Adherence segment of $1.9 million. The increase from our Automation and Analytics segment
was attributed to increases in salaries and wages of $4.0 million due to an increase in headcount, commission expenses of $1.5
million, facilities and infrastructure costs of $1.5 million, shipping costs of $1.5 million, GPO fees of $1.5 million and bad debt
expense of $1.0 million with the remainder consisting of individually insignificant administrative expenses. The increase from
our Medication Adherence segment was primarily the result of $1.0 million from the inclusion of Surgichem operations, with

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the remainder incurred from clinical studies and an increase in headcount specifically within our marketing and international
businesses.

We anticipate selling, general and administrative expenses as a percentage of total revenues to be stable throughout

2015, however this estimate could be impacted by ongoing business development activities and external macro-economic
factors.

Income from our Automation and Analytics operations increased due to an increase in product and service revenues
while operating margin increased as a result of lower cost of sales and operating expenses compared to the overall growth of
revenues.

Income from our Medication Adherence operations slightly increased due to an increase in product revenues and the

inclusion of Surgichem operations, and operating margin remained consistent with the prior year as product costs increased
which offset the relative growth in product sales.

2013 compared to 2012:

Research and development expenses increased primarily due to an increase from our Medication Adherence segment

of $4.6 million, and includes (i) a write-off of $1.8 million related to capitalized software development costs as discussed in
Note 9, Other Assets, of the Notes to Consolidated Financial Statements included in this annual report; (ii) expenses of $0.3
million related to a management reorganization within our Medication Adherence segment in the first quarter of 2013; and (iii)
the inclusion of MTS headcount, consulting and other related activities for a full year in 2013 as compared to the prior year.
Research and development expenses attributed to our Automation and Analytics segment were relatively flat compared to the
prior year.

Selling, general and administrative expenses increased due to an increase from our Automation and Analytics segment

of $11.8 million driven by headcount-related expenses including commissions of $5.0 million, facility and depreciation
expenses of $2.9 million for our new corporate headquarters and manufacturing buildings occupied in late 2012, and consulting
and professional fees of $1.8 million. Selling, general and administrative expenses increased by $7.4 million from our
Medication Adherence segment due to the inclusion of MTS general and administrative expenses for a full year in 2013 as
compared to the prior year.

Income from our Medication Adherence operations decreased due to higher product costs and operating expenses as

evidenced by the overall decline in operating margin, which was primarily due to the inclusion of MTS operations.

Provision for income taxes

Change in

2014

2013

2012

Provision for income taxes

$ 17,986

6,936

Effective tax rate on earnings

37 %

(Dollars in thousands)
$

63 % $ 11,050

32 %

153

1 % $ 10,897

40 %

Our effective tax rate was approximately 37%, 32% and 40% in 2014, 2013 and 2012, respectively.

2014 compared to 2013:

We recorded a provision for income taxes of $18.0 million and an effective tax rate of 37% for the year ended

December 31, 2014, compared to $11.1 million and an effective tax rate of 32% for the year ended December 31, 2013. The
2014 annual effective tax rate differed from the statutory tax rate of 35%, primarily due to the unfavorable impact of state
income taxes, non-deductible equity charges under ASC 740-718, and other non-deductible expenditures, including non-
deductible acquisition costs, all of which were partially offset by the domestic production activities deduction and the federal

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research tax credit, which was reinstated in December 2014, retroactive to the beginning of the year. The increase in the annual
effective tax rate as compared to 2013 was primarily due to non-deductible transaction costs incurred as a result of the
Surgichem acquisition, combined with the absence of the impact of the 2013 tax rate reduction in the U.K., as well as
reinstatement of the federal research credit in January 2013, retroactive to 2012.

2013 compared to 2012:

We recorded a provision for income taxes of approximately $11.1 million and an effective tax rate of 32% for the year
ended December 31, 2013, compared to $10.9 million and an effective tax rate of 40% for the year ended December 31, 2012.
The 2013 annual effective tax rate differed from the statutory tax rate of 35% primarily due to the favorable impact of Section
199 domestic production activity deduction, as well as the reinstatement of the federal research credit in January 2013,
retroactive to 2012, which included two years of federal research credits within the 2013 results. The decrease in the annual
effective tax rate as compared to 2012 was primarily due to the aforementioned reinstatement of the federal research and
development credit, a favorable mix in our domestic sales which decreased state apportionment factors in certain states, and the
absence of non-deductible transaction costs in 2013 that were incurred in 2012 as a result of the MTS acquisition.

Refer to Note 14, Income Taxes, of the Notes to Consolidated Financial Statements included in this annual report for

further discussion about the factors affecting our ability to realize deferred tax assets.

Sources of Cash

LIQUIDITY AND CAPITAL RESOURCES

We entered into a Credit Agreement with Wells Fargo Bank, National Association, as administrative agent, and the

lenders from time to time which provides for a $75 million revolving credit facility to be used for general corporate purposes,
including future acquisitions. The Credit Agreement permits us to request one or more increases in the aggregate commitment
provided such increases do not exceed $25 million in the aggregate.

On November 5, 2014, we entered into Amendment Number One (the “Amendment”) to the Credit Agreement. The
Amendment increases the amount of our common stock that may be repurchased by us in open market transactions authorized
by our Board of Directors, together with any repurchases of our common stock from any consultants, employees, officers or
directors of the Company or any of our subsidiaries following the death, disability, retirement or termination of employment of
such employees, officers or directors, from $25 million to $50 million per year. The Credit Agreement contains customary
affirmative and negative covenants, and financial covenants that require us to, among other things, maintain a maximum
consolidated total leverage ratio and a minimum consolidated fixed charge coverage ratio, in each case, as of the last day of
each quarter. For additional details, please refer to Note 18, Credit Agreement, of the Notes to Consolidated Financial
Statements included in this annual report.

As of December 31, 2014, we were in full compliance with all covenants, and there was no outstanding balance on the

credit facility.

Uses of Cash

Our future uses of cash are expected to be primarily for working capital, capital expenditures and other contractual

obligations. We also expect a continued use of cash for potential acquisition and acquisition assessment activities.

Our stock repurchase programs have a total of $54.9 million remaining for future repurchases as of December 31,
2014, which may result in additional use of cash. See Note 15, Stock Repurchases, of the Notes to Consolidated Financial
Statements included in this annual report. We had cash and cash equivalents of $125.9 million and $104.5 million as of
December 31, 2014 and December 31, 2013, respectively.

Based on our current business plan and revenue backlog, we believe that our existing cash and cash equivalents, our
anticipated cash flows from operations, cash generated from the exercise of employee stock options and purchases under our
employee stock purchase plan, along with the availability of funds under our $75 million Credit Agreement, will be sufficient
to meet our cash needs for working capital, capital expenditures, potential acquisitions, and other contractual obligations for at

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least the next twelve months. For periods beyond the next twelve months, we also anticipate that our net operating cash flows
plus existing balances of cash and cash equivalents will suffice to fund the continued growth of our business.

Cash Flows

The following table summarizes, for the periods indicated, selected items in our Consolidated Statements of Cash

Flows:

Net cash provided by (used in):

Operating activities

Investing activities

Financing activities

Effect of exchange rate changes on cash and cash equivalents

Net increase (decrease) in cash and cash equivalents

Operating activities

December 31,
2014

Year Ended

December 31,
2013
(In thousands)

December 31,
2012

65,163 $
(43,325 )

(206 )

(275 )
21,357 $

55,263 $
(20,452 )
7,374
33
42,218 $

39,484
(168,711 )

(232 )
10

(129,449 )

We expect cash from our operating activities to fluctuate in future periods as a result of a number of factors, including

the timing of our billings and collections, our operating results and the timing of other liability payments.

Net cash provided by operating activities was $65.2 million for 2014, primarily as a result of $30.5 million in net

income adjusted for non-cash items, including depreciation and amortization expense of $20.3 million and share-based
compensation expense of $12.8 million, an increase in deferred gross profit of $8.6 million, an increase in accrued liabilities of
$5.5 million and an increase in deferred service revenue of $5.1 million. These amounts were partially offset by an increase in
accounts receivable, net of $22.8 million.

Net cash provided by operating activities was $55.3 million for 2013, primarily as a result of $24.0 million in net

income adjusted for non-cash items, including depreciation and amortization expense of $18.4 million and share-based
compensation expense of $11.2 million.

Net cash provided by operating activities was $39.5 million for 2012, primarily as a result of $16.2 million in net

income adjusted for non-cash items, including depreciation and amortization expense of $13.3 million and share-based
compensation expense of $9.2 million.

Investing activities

Net cash used in investing activities was $43.3 million for 2014, primarily due to payments of $20.7 million for the
acquisition of Surgichem, $11.9 million for property and equipment and $10.4 million to develop software for external use.

Net cash used in investing activities was $20.5 million for 2013 and was due to payments of $12.3 million for property

and equipment and $7.8 million to develop software for external use.

Net cash used in investing activities was $168.7 million for 2012 and was primarily due to payments of $156.3 million

for the acquisition of MTS Medication Technologies, Inc. and $15.1 million for property and equipment.

Financing activities

Net cash used in financing activities was $0.2 million for 2014 as a result of $24.1 million in repurchases of our

common stock, partially offset by $21.8 million in net proceeds from sales of common stock through employee stock plans.

Net cash provided by financing activities was $7.4 million for 2013 as a result of $26.9 million in net proceeds from
sales of common stock through employee stock plans, partially offset by $21.0 million in repurchases of our common stock.

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Net cash used in financing activities was $0.2 million for 2012 as a result of $12.4 million in repurchases of our

common stock, partially offset by $10.2 million in net proceeds from sales of common stock through employee stock plans.

Contractual Obligations

We had $48.0 million in contractual commitments to third parties for non-cancelable operating leases, commitments to

contract manufacturers and suppliers and other purchase commitments as of December 31, 2014 as follows:

Operating leases (1)
Purchase obligations (2)

Total (3)

_________________________________________________

Payments Due by Period

Total

2015

2016 and 2017

2018 and 2019

2020 and
Thereafter

38,638 $
9,325
47,963 $

(In thousands)

5,637 $
9,325
14,962 $

10,463 $
—
10,463 $

9,547 $
—
9,547 $

12,991
—
12,991

(1)

(2)

(3)

Commitments under operating leases relate primarily to leasehold property and office equipment. Rent expense was
$6.8 million, $6.9 million and $5.7 million for the years ended December 31, 2014, December 31, 2013 and
December 31, 2012, respectively.

We purchase components from a variety of suppliers and use contract manufacturers to provide manufacturing
services for our products. During the normal course of business, we issue purchase orders with estimates of our
requirements several months ahead of the delivery dates. These amounts are associated with agreements that are
enforceable and legally binding. The amounts under such contracts are included in the table above because we believe
that cancellation of these contracts is unlikely and we expect to make future cash payments according to the contract
terms or in similar amounts for similar materials.

We have recorded $5.9 million for uncertain tax positions under long-term liabilities as of December 31, 2014 in
accordance with the authoritative guidance summarized in the section entitled "Critical Accounting Policies and
Estimates" above. As these liabilities do not reflect actual tax assessments, the timing and amount of payments we
might be required to make will depend upon a number of factors. Accordingly, as the timing and amount of payment
cannot be estimated, $5.9 million in uncertain tax position liabilities have not been included in the table above. See
Note 14, Income Taxes, of the Notes to Consolidated Financial Statements included in this annual report.

See Note 12, Commitments, of the Notes to Consolidated Financial Statements included in this annual report.

Off-Balance Sheet Arrangements

As of December 31, 2014, we had no off-balance sheet arrangements as defined under Regulation S-K 303(a)(4) of the

Securities Exchange Act of 1934, as amended, and the instructions thereto.

ITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

We are exposed to market risks related to fluctuations in foreign currency exchange rates and interest rates.

Foreign Currency Exchange Rate Risk

We conduct business through our worldwide operations, and therefore we are exposed to foreign currency risk for
transactions denominated in the Euro, British pound, Canadian dollar, Australian dollar and Chinese renminbi, which may
adversely impact our financial results. Our cash flow, results of operations and certain intercompany balances that are exposed
to foreign exchange rate fluctuations may differ from expectations, and we may record gains or losses due to foreign currency
fluctuations.

Interest Rate Risk

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We had $125.9 million of cash and cash equivalents as of December 31, 2014. We invest our cash in cash investments

with original or remaining maturities of three months or less and whose principal is not subject to market rate fluctuations.
Accordingly, interest rate declines would adversely affect our interest income but would not affect the carrying value of our
cash investments. The effective weighted interest rate was less than 1% for the year ended December 31, 2014. Management
considers this interest rate exposure to be immaterial.

ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

The Consolidated Financial Statements and related disclosures included in Part IV, Item 15 of this annual report are

incorporated by reference into this Item 8.

ITEM 9. CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL
DISCLOSURE

Change in Independent Registered Public Accounting Firm

In April 2014, the Audit Committee of our Board of Directors dismissed Ernst & Young LLP ("E&Y"), as our
independent registered public accounting firm and engaged Deloitte & Touche LLP ("Deloitte"). E&Y’s reports on our
consolidated financial statements for 2012 and 2013 did not contain an adverse opinion or disclaimer of opinion and were not
qualified or modified as to uncertainty, audit scope, or accounting principles. In connection with the audits of our financial
statements for the years ended December 31, 2013 and December 31, 2012, and in the subsequent interim period through April
7, 2014, there were no disagreements with E&Y on any matter of accounting principles or practices, financial statement
disclosure, or auditing scope or procedures, which if not resolved to the satisfaction of E&Y, would have caused E&Y to make
reference to the subject matter in connection with its reports. There were no "reportable events" as that term is described in
Item 304(a)(1)(v) of Regulation S-K issued by the SEC.

During the fiscal years ended December 31, 2013 and December 31, 2012, and the subsequent interim period through

April 7, 2014, neither the Company nor anyone acting on its behalf has consulted with Deloitte with respect to (i) the
application of accounting principles to a specified transaction, either completed or proposed, or the type of audit opinion that
might be rendered on the Company’s financial statements, and neither a written report nor oral advice was provided to the
Company that Deloitte concluded was an important factor considered by the Company in reaching a decision as to any
accounting, auditing, or financial reporting issue or (ii) any matter that was either the subject of a “disagreement” or “reportable
event” as those terms are defined in Item 304(a)(1) of Regulation S-K.

ITEM 9A. CONTROLS AND PROCEDURES

Evaluation of Disclosure Controls and Procedures

Our management, with the participation of our principal executive officer and principal financial officer, evaluated the

effectiveness of our disclosure controls and procedures (as such term is defined in Rules 13a-15(e) and 15d-15(e) under the
Securities Exchange Act of 1934, as amended, or the Exchange Act) as of the end of the period covered by this annual report.
These disclosure controls and procedures are designed to ensure that the information required to be disclosed by us in this
annual report was (i) recorded, processed, summarized and reported within the time periods specified in the SEC's rules and
regulations and (ii) accumulated and communicated to our management, including our principal executive officer and principal
financial officer, to allow timely decisions regarding required disclosure.

Based on such evaluation, our principal executive officer and principal financial officer have concluded that our

disclosure controls and procedures were effective at the reasonable assurance level as of December 31, 2014.

Management's Report on Internal Control Over Financial Reporting

Our management is responsible for establishing and maintaining adequate internal control over financial reporting (as

such term is defined in Rules 13a-15(f) and 15d-15(f) under the Exchange Act). Our internal control system is designed to
provide reasonable assurance regarding the preparation and fair presentation of financial statements for external purposes in

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accordance with U.S. generally accepted accounting principles. All internal control systems, no matter how well designed, have
inherent limitations and can provide only reasonable assurance that the objectives of the internal control system are met.

Under the supervision and with the participation of our management, including our principal executive officer and

principal financial officer, we conducted an evaluation of the effectiveness of our internal control over financial reporting as of
December 31, 2014 using the criteria for effective internal control over financial reporting as described in "Internal Control—
Integrated Framework," issued by the Committee of Sponsoring Organization of the Treadway Commission (2013 framework)
(the COSO Criteria). Based on this assessment, management concluded that our internal control over financial reporting was
effective as of December 31, 2014.

Our independent registered public accounting firm, Deloitte & Touche LLP, has issued its attestation report on our

internal control over financial reporting as of December 31, 2014, which is included in Part IV, Item 15 of this annual report.

Changes in Internal Control Over Financial Reporting

There have been no changes in our internal control over financial reporting (as such term is defined in Rules 13a-15(f)

and 15d-15(f) under the Exchange Act) that have materially affected, or are reasonably likely to materially affect, our internal
control over financial reporting during the year ended December 31, 2014.

ITEM 9B. OTHER INFORMATION

None.

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PART III

Certain information required by Part III is omitted from this annual report because the registrant will file with the
U.S. Securities and Exchange Commission a definitive proxy statement pursuant to Regulation 14A in connection with the
solicitation of proxies for the Company's Annual Meeting of Stockholders expected to be held in May 2015 (the "Proxy
Statement") not later than 120 days after the end of the fiscal year covered by this annual report, and certain information
included therein is incorporated herein by reference.

ITEM 10. DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE

The information required by this Item with respect to directors and executive officers may be found under the heading
"Executive Officers of the Registrant" in Part I, Item 1 of this annual report, and in the section entitled "Election of Directors"
appearing in the Proxy Statement. Such information is incorporated herein by reference.

The information required by this Item with respect to our audit committee and audit committee financial expert may

be found in the section entitled "Information Regarding the Board of Directors and Corporation Governance—Audit
Committee" appearing in the Proxy Statement. Such information is incorporated herein by reference.

The information required by this Item with respect to compliance with Section 16(a) of the Securities Exchange Act of
1934 may be found in the sections entitled "Section 16(a) Beneficial Ownership Reporting Compliance" appearing in the Proxy
Statement. Such information is incorporated herein by reference.

Our written Code of Conduct applies to all of our directors and employees, including executive officers, including

without limitation our principal executive officer, principal financial officer, principal accounting officer or controller or
persons performing similar functions. The Code of Conduct is available on our website at www.omnicell.com under the
hyperlink titled "Corporate Governance." Changes to or waivers of the Code of Conduct will be disclosed on the same website.
We intend to satisfy the disclosure requirement under Item 5.05 of Form 8-K regarding any amendment to, or waiver of, any
provision of the Code of Conduct by disclosing such information on the same website.

ITEM 11. EXECUTIVE COMPENSATION

The information required by this Item with respect to director and executive officer compensation is incorporated by

reference to the section of our Proxy Statement under the section entitled "Executive Compensation—Compensation
Discussion and Analysis."

The information required by this Item with respect to Compensation Committee interlocks and insider participation is

incorporated herein by reference to the information from the Proxy Statement under the section entitled "Information
Regarding the Board of Directors and Corporate Governance—Compensation Committee Interlocks and Insider Participation."

The information required by this Item with respect to our Compensation Committee's review and discussion of the

Compensation Discussion and Analysis included in the Proxy Statement is incorporated herein by reference to the information
from the Proxy Statement under the section entitled "Executive Compensation—Compensation Discussion and Analysis—
Compensation Committee Report."

ITEM 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED
STOCKHOLDERS MATTERS

The information required by this Item with respect to security ownership of certain beneficial owners and management
is incorporated herein by reference to the information from the Proxy Statement under the section entitled "Security Ownership
of Certain Beneficial Owners and Management."

The information required by this Item with respect to securities authorized for issuance under our equity compensation

plans is incorporated herein by reference to the information from the Proxy Statement under the section entitled "Equity
Compensation Plan Information."

ITEM 13. CERTAIN RELATIONSHIPS, RELATED TRANSACTIONS AND DIRECTOR INDEPENDENCE

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The information required by this Item with respect to related party transactions is incorporated herein by reference to

the information from the Proxy Statement under the section entitled "Certain Relationships and Related Transactions."

The information required by this Item with respect to director independence is incorporated herein by reference to the
information from the Proxy Statement under the section entitled "Information Regarding the Board of Directors and Corporate
Governance—Independence of the Board of Directors."

ITEM 14. PRINCIPAL ACCOUNTANT FEES AND SERVICES

The information required by this Item is incorporated herein by reference to the section from the Proxy Statement

under the section entitled "Ratification of Selection of Independent Registered Public Accounting Firm—Principal Accountant
Fees and Services."

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PART IV

ITEM 15. EXHIBITS AND FINANCIAL STATEMENT SCHEDULES

The following documents are included as part of this annual report:

(1)

Consolidated Financial Statements:

Index to Financial Statements

Page Number

Reports of Independent Registered Public Accounting Firms

Consolidated Balance Sheets as of December 31, 2014 and December 31, 2013

Consolidated Statements of Operations for the years ended December 31, 2014, December 31, 2013 and
December 31, 2012
Consolidated Statements of Comprehensive Income for the years ended December 31, 2014, December 31,
2013 and December 31, 2012
Consolidated Statements of Stockholders' Equity for the years ended December 31, 2014, December 31, 2013
and December 31, 2012
Consolidated Statements of Cash Flows for the years ended December 31, 2014, December 31, 2013 and
December 31, 2012
Notes to Consolidated Financial Statements

The foregoing additional financial statement schedule should be considered in conjunction with our
Consolidated Financial Statements. All other schedules have been omitted because the required information is
either not applicable or not sufficiently material to require submission of the schedule.
Financial Statement Schedule II: Valuation and Qualifying Accounts

(2)

Exhibits: The information required by this item is set forth on the exhibit index which follows the signature page of
this report.

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REPORTS OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRMS

To the Board of Directors and Stockholders of
Omnicell, Inc.
Mountain View, California

We have audited the accompanying consolidated balance sheet of Omnicell, Inc. and subsidiaries (the "Company") as
of December 31, 2014, and the related consolidated statements of operations, comprehensive income, stockholders' equity, and
cash flows for the year then ended. Our audit also included the financial statement schedule for the year ended December 31,
2014 listed in the Index at Item 15. These financial statements and the financial statement schedule are the responsibility of the
Company's management. Our responsibility is to express an opinion on these financial statements based on our audit.

We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United

States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial
statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the amounts and
disclosures in the financial statements. An audit also includes assessing the accounting principles used and significant estimates
made by management, as well as evaluating the overall financial statement presentation. We believe that our audit provides a
reasonable basis for our opinion.

In our opinion, such 2014 consolidated financial statements present fairly, in all material respects, the financial
position of Omnicell, Inc. and subsidiaries as of December 31, 2014, and the results of their operations and their cash flows for
the year then ended in conformity with accounting principles generally accepted in the United States of America. Also, in our
opinion, such financial statement schedule for the year ended December 31, 2014, when considered in relation to the basic
consolidated financial statements taken as a whole, presents fairly, in all material respects, the information set forth therein.

We have also audited, in accordance with the standards of the Public Company Accounting Oversight Board (United
States), the Company's internal control over financial reporting as of December 31, 2014, based on the criteria established in
Internal Control - Integrated Framework (2013) issued by the Committee of Sponsoring Organizations of the Treadway
Commission and our report dated March 30, 2015 expressed an unqualified opinion on the Company's internal control over
financial reporting.

/s/ DELOITTE & TOUCHE LLP

San Jose, California
March 30, 2015

F-1

Table of Contents

To the Board of Directors and Stockholders of
Omnicell, Inc.
Mountain View, California

We have audited the internal control over financial reporting of Omnicell, Inc. and subsidiaries (the "Company") as of
December 31, 2014, based on criteria established in Internal Control - Integrated Framework (2013) issued by the Committee
of Sponsoring Organizations of the Treadway Commission. The Company's management is responsible for maintaining
effective internal control over financial reporting and for its assessment of the effectiveness of internal control over financial
reporting, included in the accompanying Management’s Report on Internal Control over Financial Reporting. Our
responsibility is to express an opinion on the Company's internal control over financial reporting based on our audit.

We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United

States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether effective
internal control over financial reporting was maintained in all material respects. Our audit included obtaining an understanding
of internal control over financial reporting, assessing the risk that a material weakness exists, testing and evaluating the design
and operating effectiveness of internal control based on the assessed risk, and performing such other procedures as we
considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion.

A company's internal control over financial reporting is a process designed by, or under the supervision of, the

company's principal executive and principal financial officers, or persons performing similar functions, and effected by the
company's board of directors, management, and other personnel 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 (1)
pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of
the assets of the company; (2) 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 expenditures of the
company are being made only in accordance with authorizations of management and directors of the company; and (3) 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 the inherent limitations of internal control over financial reporting, including the possibility of collusion or
improper management override of controls, material misstatements due to error or fraud may not be prevented or detected on a
timely basis. Also, projections of any evaluation of the effectiveness of the internal control over financial reporting to future
periods are subject to the risk that the controls may become inadequate because of changes in conditions, or that the degree of
compliance with the policies or procedures may deteriorate.

In our opinion, the Company maintained, in all material respects, effective internal control over financial reporting as

of December 31, 2014, based on the criteria established in Internal Control - Integrated Framework (2013) issued by the
Committee of Sponsoring Organizations of the Treadway Commission.

We have also audited, in accordance with the standards of the Public Company Accounting Oversight Board (United

States), the consolidated financial statements and financial statement schedule as of and for the year ended December 31, 2014
of the Company and our report dated March 30, 2015 expressed an unqualified opinion on those financial statements and
financial statement schedule.

/s/ DELOITTE & TOUCHE LLP

San Jose, California
March 30, 2015

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Table of Contents

To the Board of Directors and Stockholders of Omnicell, Inc.

We have audited the accompanying consolidated balance sheets of Omnicell, Inc. as of December 31, 2013, and the

related consolidated statements of operations, comprehensive income, stockholders' equity, and cash flows for each of the two
years in the period ended December 31, 2013. Our audits also included the financial statement schedule as of December 31,
2013 and 2012 listed in the index at 15(a)(1). These financial statements and schedule are the responsibility of the Company's
management. Our responsibility is to express an opinion on these financial statements and schedule based on our audits.

We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board

(United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the
financial statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the
amounts and disclosures in the financial statements. An audit also includes assessing the accounting principles used and
significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that
our audits provide a reasonable basis for our opinion.

In our opinion, the financial statements referred to above present fairly, in all material respects, the consolidated

financial position of Omnicell, Inc. at December 31, 2013, and the consolidated results of its operations and its cash flows for
each of the two years in the period ended December 31, 2013, in conformity with U.S. generally accepted accounting
principles. Also, in our opinion, the related financial statement schedule as of December 31, 2013 and 2012, when considered
in relation to the basic financial statements as a whole, presents fairly in all material respects the information set forth therein.

/s/ Ernst & Young LLP

San Jose, California
March 17, 2014,
except for Note 8 and 17, as to which the date is
March 30, 2015

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Table of Contents

OMNICELL, INC.

CONSOLIDATED BALANCE SHEETS

Current assets:

Cash and cash equivalents

Accounts receivable, net of allowances of $1,206 and $490, respectively

ASSETS

Inventories, net

Prepaid expenses

Deferred tax assets

Other current assets

Total current assets
Property and equipment, net

Long-term net investment in sales-type leases

Goodwill

Intangible assets, net

Long-term deferred tax assets

Other long-term assets

Total assets

Current liabilities:

Accounts payable

Accrued compensation

Accrued liabilities

Deferred service revenue

Deferred gross profit

Total current liabilities

LIABILITIES AND STOCKHOLDERS’ EQUITY

Long-term deferred service revenue

Long-term deferred tax liabilities

Other long-term liabilities

Total liabilities

Commitments and contingencies (Notes 12 & 13)

Stockholders’ equity:

Common stock, $0.001 par value, 100,000 shares authorized; 43,540 and 41,840 shares
issued; 35,816 and 35,004 shares outstanding, respectively
Treasury stock at cost, 7,721 and 6,837 shares outstanding, respectively

Additional paid-in capital

Retained earnings

Accumulated other comprehensive income

Total stockholders’ equity

Total liabilities and stockholders’ equity

December 31,
2014

December 31,
2013

(In thousands, except par value)

125,888 $
82,763
31,554
23,518
12,446
7,215
283,384
36,178
10,848
122,720
82,667
1,144
23,273
560,214 $

19,432 $
19,874
19,299
25,167
28,558
112,330
20,308
30,454
7,024
170,116

104,531
58,597
31,457
18,883
12,635
7,675
233,778
35,254
11,485
111,343
81,602
1,102
17,937
492,501

16,471
19,604
13,746
22,626
19,957
92,404
17,763
28,162
5,175
143,504

(135,053 )
457,436
69,033
(1,361 )
390,098
560,214 $

(110,962 )
421,232
38,515
171
348,997
492,501

The accompanying Notes to Consolidated Financial Statements are an integral part of these statements.

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Table of Contents

OMNICELL, INC.

CONSOLIDATED STATEMENTS OF OPERATIONS

Year Ended

December 31,
2014

December 31,
2013
(In thousands, except per share data)

December 31,
2012

Revenues:

Product

Services and other revenues

Total revenues

Cost of revenues:

Cost of product revenues

Cost of services and other revenues

Total cost of revenues

Gross profit

Operating expenses:

Research and development

Selling, general and administrative

Total operating expenses

Income from operations

Interest and other (expense), net

Income before provision for income taxes

Provision for income taxes

Net income

Net income per share:

Basic

Diluted

Weighted-average shares:

Basic

Diluted

360,344 $
80,556
440,900

307,189 $
73,396
380,585

173,419
33,621
207,040
233,860

27,802
156,475
184,277
49,583
(1,079 )
48,504
17,986
30,518 $

144,997
32,189
177,186
203,399

29,105
138,995
168,100
35,299
(270 )
35,029
11,050
23,979 $

0.86 $
0.83 $

0.69 $
0.67 $

35,650
36,622

34,736
35,777

247,654
66,373
314,027

112,369
31,070
143,439
170,588

23,726
119,736
143,462
27,126
(51 )
27,075
10,897
16,178

0.49
0.47

33,307
34,213

The accompanying Notes to Consolidated Financial Statements are an integral part of these statements.

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Table of Contents

OMNICELL, INC.

CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME

Net income

Other comprehensive income (loss), net of reclassification adjustments:

Unrealized losses on securities

Unrealized gains (losses) on foreign currency forward contracts

Foreign currency translation adjustments

Other comprehensive income (loss), net of tax:

Comprehensive income

December 31,
2014

Year Ended

December 31,
2013
(In thousands)

December 31,
2012

30,518 $

23,979 $

16,178

—
—
(1,532 )

(1,532 )
28,986 $

—
(65 )
105
40
24,019 $

(1 )
65
66
130
16,308

The accompanying Notes to Consolidated Financial Statements are an integral part of these statements.

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Table of Contents

OMNICELL, INC.

CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY

Common Stock

Treasury Stock

Amount

Additional
Paid-In
Capital

Accumulated
Earnings
(Deficit)

(In thousands)

Accumulated
Other
Comprehensive
Income

Stockholders'
Equity

Balances as of
December 31, 2011

Net income

38,236
—

Other comprehensive
income
Stock repurchases

Share-based
compensation
Issuance of common
stock under employee
stock plans
Tax payments related to
restricted stock units
Income tax benefits
from employee stock
plans

Balances as of
December 31, 2012

Net income

Other comprehensive
income
Stock repurchases

Share-based
compensation
Issuance of common
stock under employee
stock plans
Tax payments related to
restricted stock units
Income tax benefits
from employee stock
plans

Balances as of
December 31, 2013

Net income

Other comprehensive
income
Stock repurchases

Share-based
compensation
Issuance of common
stock under employee
stock plans
Tax payments related to
restricted stock units
Income tax benefits
from employee stock
plans

—
—

—

1,258

—

39,493
—

—
—

—

2,349

—

41,842
—

—
—

—

1,695

—

Balances as of
December 31, 2014

43,537

38
—

—
—

—

39
—

—
—

—

41
—

—
—

—

(5,054 ) $ (77,637 ) $ 362,154
—

—

(1,642 ) $
16,178

1
—

282,914
16,178

—

(898 )

(12,363 )

—
—

—

9,214

—

10,190

(1,241 )

—

2,527

—
—

—

130
—

—

130

(12,363 )

9,214

10,191

(1,241 )

2,527

(5,952 ) $ (90,000 ) $ 382,844
—

—

14,536
23,979

131
—

307,550
23,979

—

(885 )

(20,962 )

—
—

—

11,151

—

26,884

(2,223 )

—

2,576

—
—

—

40
—

—

(20,962 )

11,151

26,886

(2,223 )

2,576

(6,837 ) $ (110,962 ) $ 421,232
—

—

38,515
30,518

171
—

348,997
30,518

—

(884 )

(24,091 )

—
—

(1,532 )
—

—

12,785

—

21,793

(3,744 )

—

5,370

—

(1,532 )

(24,091 )

12,785

21,795

(3,744 )

5,370

(7,721 ) $ (135,053 ) $ 457,436

69,033

(1,361 ) $

390,098

The accompanying Notes to Consolidated Financial Statements are an integral part of these statements.

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Table of Contents

OMNICELL, INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS

Operating Activities
Net income

Adjustments to reconcile net income to net cash provided by operating
activities:

Depreciation and amortization

Loss on disposal of fixed assets

Impairment of software development costs and equity investments

Provision for receivable allowance

Share-based compensation expense

Income tax benefits from employee stock plans

Excess tax benefits from employee stock plans

Provision for excess and obsolete inventories

Deferred income taxes

Changes in operating assets and liabilities, net of business acquisitions:

Accounts receivable, net

Inventories

Prepaid expenses

Other current assets

Net investment in sales-type leases

Other assets

Accounts payable

Accrued compensation

Accrued liabilities

Deferred service revenue

Deferred gross profit

Other long-term liabilities

Net cash provided by operating activities

Investing Activities

Maturities of short-term investments

Acquisition of intangible assets and intellectual property

Software development for external use

Purchases of property and equipment

Business acquisition, net of cash acquired

Net cash used in investing activities

Financing Activities

Proceeds from issuances under stock-based compensation plans

Employees' taxes paid related to restricted stock units

Common stock repurchases

Excess tax benefits from employee stock plans

Net cash provided by (used in) financing activities

Effect of exchange rate changes on cash and cash equivalents

F-8

December 31,
2014

Year Ended

December 31,
2013
(In thousands)

December 31,
2012

30,518 $

23,979 $

16,178

20,272
167
350
941
12,785
5,370
(5,834 )
542
1,402

(22,799 )
1,418
(4,296 )
53
1,048
297
1,611
270
5,512
5,086
8,601
1,849
65,163

—
(327 )

(10,353 )

(11,922 )

(20,723 )

(43,325 )

21,795
(3,744 )

(24,091 )
5,834

(206 )

(275 )

18,365
345
1,759
110
11,151
2,576
(3,673 )
856
787

(3,609 )

(5,410 )

(3,491 )
1,566
1,723
630
(1,784 )
7,991
1,758
82
(815 )
367
55,263

—
(356 )

(7,761 )

(12,335 )
—
(20,452 )

26,886
(2,223 )

(20,962 )
3,673
7,374
33

13,325
66
—
582
9,214
2,527
(3,182 )
394
2,718

(9,311 )
2,536
(4,897 )

(1,114 )

(4,154 )

(3,831 )
1,751
4,285
674
2,914
6,562
2,247
39,484

8,122
(373 )

(5,028 )

(15,120 )

(156,312 )

(168,711 )

10,190
(1,241 )

(12,363 )
3,182

(232 )
10

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Net increase (decrease) in cash and cash equivalents

Cash and cash equivalents at beginning of period

Cash and cash equivalents at end of period

Supplemental cash flow information
Cash paid for interest

Cash paid for taxes, net of refunds

Supplemental disclosure of non-cash investing activities
Purchases of property and equipment

21,357
104,531
125,888 $

42,218
62,313
104,531 $

(129,449 )
191,762
62,313

61 $
9,161 $

122 $
7,062 $

28
6,676

273 $

1,696 $

—

The accompanying Notes to Consolidated Financial Statements are an integral part of these statements.

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Table of Contents

OMNICELL, INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

Note 1. Summary of Significant Accounting Policies

Business

Omnicell, Inc. was incorporated in California in 1992 under the name Omnicell Technologies, Inc. and reincorporated

in Delaware in 2001 as Omnicell, Inc. Our major products are automated medication, supply control systems and medication
adherence solutions which are sold in our principal market, which is the healthcare industry. Our market is primarily located in
the United States and Canada. "Omnicell," "our," "us," "we," or the "Company" collectively refer to Omnicell, Inc. and its
subsidiaries.

Principles of consolidation

The accompanying Consolidated Financial Statements have been prepared in accordance with U.S. GAAP and include

all adjustments necessary for the fair presentation of the Company's consolidated financial position, results of operations and
cash flows for the periods presented. The Consolidated Financial Statements include the accounts of the Company and its
subsidiaries. All intercompany accounts and transactions have been eliminated in consolidation. The results of companies
acquired during the year are included in the Consolidated Financial Statements from the effective date of acquisition.

Use of estimates

The preparation of financial statements in accordance with U.S. GAAP requires management to make estimates and

assumptions that affect the amounts reported in our Consolidated Financial Statements and accompanying Notes. Management
bases its estimates on historical experience and various other assumptions believed to be reasonable. Although these estimates
are based on management's best knowledge of current events and actions that may impact the company in the future, actual
results may be different from the estimates. Our critical accounting policies are those that affect our financial statements
materially and involve difficult, subjective or complex judgments by management. Those policies are revenue recognition,
share-based compensation, inventory valuation, valuation of goodwill, purchased intangibles and long-lived assets, and
accounting for income taxes.

Segment reporting change

We modified our segment reporting structure to match our operating structure based on how our Chief Operating
Decision Maker (“CODM”) views the business and allocates resources, beginning in the first quarter of 2014. The CODM
function is our Chief Executive Officer. Retrospective adjustments of prior period financial information have been made to
conform to the current period presentation. This change does not impact previously reported Consolidated Financial Statements
of the Company. See Note 17, Segment Information, for additional information on our segment reporting change.

Foreign currency translation

We translate the assets and liabilities of our non-U.S. dollar functional currency subsidiaries into U.S. dollars using
exchange rates in effect at the end of each period. Revenue and expenses for these subsidiaries are translated using rates that
approximate those in effect during the period. Gains and losses from these translations are recorded as foreign currency
translation adjustments and included in accumulated other comprehensive income in stockholders’ equity.

Revenue recognition

We earn revenues from sales of our medication and medical and surgical supply automation systems along with

consumables and related services, which are sold in the healthcare industry, our principal market. Revenues related to
consumable products are reported net of discounts provided to our customers. Our customer arrangements typically include one
or more of the following deliverables:

Products. Software-enabled equipment that manages and regulates the storage and dispensing of pharmaceuticals,

consumable blister cards and packaging equipment and other medical supplies.

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Software. Additional software applications that enable incremental functionality of our equipment.

Installation. Installation of equipment as integrated systems at customers' sites.

Post-installation technical support. Phone support, on-site service, parts and access to unspecified software upgrades

and enhancements, if and when available.

Professional services. Other customer services, such as training and consulting.

We recognize revenue when the earnings process is complete, based upon our evaluation of whether the following four

criteria have been met:

Persuasive evidence of an arrangement exists. We use signed customer contracts and signed customer purchase orders

as evidence of an arrangement for leases and sales. For service engagements, we use a signed services agreement and a
statement of work to evidence an arrangement.

Delivery has occurred. Equipment and embedded software product delivery is deemed to occur upon successful
installation and receipt of a signed and dated customer confirmation of installation letter, providing evidence that we have
delivered what a customer ordered. In instances of a customer self-installation, product delivery is deemed to have occurred
upon receipt of a signed and dated customer confirmation letter. If a sale does not require installation, we recognize revenue on
delivery of products to the customer, including transfer of title and risk of loss, assuming all other revenue criteria are met. For
existing distributors, where installation of equipment training has been previously provided and the distributor is certified to
install our equipment at the end-user customer facility, we recognize revenue from sales of products to the distributor upon
shipment assuming all other revenue criteria are met since we do not allow for rights of return or refund. For new distributors,
where we have not provided installation of equipment training, revenue on the sales of products to the distributor is deferred
until the distributor has completed the Distributor Training Program and has been certified to install our equipment at the end-
user facility. For the sale of consumable blister cards, we recognize revenue when title and risk of loss of the products shipped
have transferred to the customer, which usually occurs upon shipment from our facilities. Assuming all other revenue criteria
are met, we recognize revenue for support services ratably over the related support services contract period. We recognize
revenue on training and professional services as they are performed.

Fee is fixed or determinable. We assess whether a fee is fixed or determinable at the outset of the arrangement based

on the payment terms associated with the transaction. We have established a history of collecting under the original contract
without providing concessions on payments, products or services.

In arrangements with multiple deliverables, assuming all other revenue criteria are met, we recognize revenue for

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The relative selling price method allocates total arrangement consideration proportionally to each deliverable on the
basis of its estimated selling price. In addition, the amount recognized for any delivered items cannot exceed that which is not
contingent upon delivery of any remaining items in the arrangement.

A portion of our sales are made through multi-year lease agreements. Under sales-type leases, we recognize revenue

for our hardware and software products net of lease execution costs such as post-installation product maintenance and technical
support, at the net present value of the lease payment stream once our installation obligations have been met. We optimize cash
flows by selling a majority of our non-U.S. government leases to third-party leasing finance companies on a non-recourse basis.
We have no obligation to the leasing company once the lease has been sold. Some of our sales-type leases, mostly those
relating to U.S. government hospitals, are retained in-house. Interest income in these leases is recognized in product revenue
using the effective interest method.

Financial Instruments

For assets and liabilities measured at fair value, such amounts are based on an expected exit price representing the

amount that would be received from the sale of an asset or paid to transfer a liability in a transaction between market
participants. As such, fair value may be based on assumptions that market participants would use in pricing an asset or liability.
The authoritative guidance on fair value measurements establishes a consistent framework for measuring fair value on either a
recurring or nonrecurring basis whereby inputs used in valuation techniques are assigned a hierarchical level. The following
methods were used to estimate the fair value of each class of financial instruments for which it is practical to estimate that
value:

Cash equivalents. We classify investments as cash equivalents if their original or remaining contractual maturity is

three months or less at the date of purchase. Cash equivalents are carried at amounts that approximate fair value due to the short
period of time to maturity. Our cash equivalents are maintained in demand deposit accounts with financial institutions of high
credit quality, and are invested in institutional money market funds, short-term bank time deposits and similar short duration
instruments with fixed maturities. We continuously monitor the creditworthiness of the financial institutions and institutional
money market funds in which we invest. We have not experienced any credit losses from our cash investments.

Marketable securities. Our marketable securities and investments are classified as available-for-sale, and unrealized

gains and losses, net of tax, are included in accumulated other comprehensive income.

Equity investments. We make equity investments in privately-held companies whose businesses are complementary to

our business. The investment in which we hold less than 20% of the voting stock outstanding and do not exert significant
influence is accounted for under the cost method of accounting. The cost amount of this investment was $0.4 million as of
December 31, 2014 and December 31, 2013, and was no longer realizable as of December 31, 2014 and therefore considered
impaired as discussed in Note 9, Other Assets. We invested $0.9 million to purchase 15% of our United Kingdom automation
and analytics products distributor’s outstanding equity. We record this investment under the equity method of accounting as we
have the right to appoint a member to this company's board of directors as well as certain other voting rights and, therefore, we
believe we have the ability to exert significant influence over this distributor's operations. Our proportionate equity share of the
income of this distributor, recognized in interest and other income, net was immaterial for the years ended December 31, 2014,
December 31, 2013 and December 31, 2012. Our equity investments are included in other long-term assets. We assess the
recoverability of these investments by reviewing various indicators for other-than-temporary impairment.

Foreign currency forward contracts. We enter into foreign currency forward contracts to protect our business from the
risk that exchange rates may affect the eventual cash flows resulting from intercompany transactions between Omnicell and our
foreign subsidiaries. These transactions primarily arise as a result of products manufactured in the United States and sold to
foreign subsidiaries in U.S. dollars rather than the subsidiaries' functional currencies. These forward contracts are considered to

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be financial derivative instruments and are recorded at fair value. Changes in fair values of these financial derivative
instruments are either recognized in other comprehensive income or net income depending on whether the derivative has been
designated and qualifies as a hedging instrument. We had no foreign currency forward contracts which qualify for hedge
accounting as of December 31, 2014 and December 31, 2013, and had no foreign currency forward contracts as of December
31, 2014.

Debt. Our debt includes a $75 million revolving credit facility. Borrowings under our revolving credit facility would
be recognized at cost plus accrued interest based upon stated interest rates. We have not yet drawn any funds under the credit
facility to date.

Accounts receivable and notes receivable (net investment in sales-type leases)

We actively manage our accounts receivable to minimize credit risk. We typically sell to customers for which there is a
history of successful collection. New customers are subject to a credit review process, which evaluates that customer's financial
position and ability to pay. We continually monitor and evaluate the collectability of our trade receivables based on a
combination of factors. We record specific allowances for doubtful accounts when we become aware of a specific customer's
impaired ability to meet its financial obligation to us, such as in the case of bankruptcy filings or deterioration of financial
position. There were no significant customers that accounted for more than 10% of our accounts receivable as of December 31,
2014 and December 31, 2013.

Uncollectible amounts are charged off against trade receivables and the allowance for doubtful accounts when we

make a final determination that there is no reasonable expectation of recovery. Estimates are used in determining our
allowances for all other customers based on factors such as current trends, the length of time the receivables are past due and
historical collection experience. While we believe that our allowance for doubtful accounts receivable is adequate and that the
judgment applied is appropriate, such estimated amounts could differ materially from what will actually be uncollectible in the
future.

Sales of accounts receivable

We record the sale of our accounts receivables as "true sales" in accordance with accounting guidance for transfers and

servicing of financial assets. We transferred non-recourse accounts receivable totaling $62.0 million, $41.3 million and $60.9
million as of December 31, 2014, December 31, 2013 and December 31, 2012, respectively, which approximated fair value, to
leasing companies on a non-recourse basis. Accounts receivable included approximately $1.1 million, $0.1 million and $0.7
million due from third-party leasing companies for transferred non-recourse accounts receivable as of December 31, 2014,
December 31, 2013 and December 31, 2012, respectively.

Inventory

Inventories are stated at the lower of cost (utilizing standard costs, applying the first-in, first-out method) or market.

Cost elements included in inventory are direct labor and materials plus applied overhead. We routinely assess on-hand
inventory for timely identification and measurement of obsolete, slow-moving or otherwise impaired inventory. We write down
our inventory for estimated obsolescence, excess or unmarketable quantities equal to the difference between the cost of the
inventory and its estimated market value based on assumptions about future demand and market conditions. If actual future
demand or market conditions are less favorable than we projected, additional inventory write-downs may be required.

Property and equipment

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Property and equipment less accumulated depreciation are stated at historical cost. Our expenditures for property and

equipment are for computer equipment and software used in the administration of our business, and for leasehold
improvements to our leased facilities. We also develop molds and dies used in long-term manufacturing arrangements with
suppliers and for production automation equipment used in the manufacturing of consumable blister card components.
Depreciation and amortization of property and equipment are provided over their estimated useful lives, using the straight-line
method, as follows:

Computer equipment and related software

3 - 5 years

Leasehold and building improvements

Shorter of the lease term or the estimated useful life

Furniture and fixtures

Equipment

5 - 7 years

3 - 12 years

We capitalize costs related to computer software developed or obtained for internal use in accordance with ASC 350-

40, Internal-Use Software. Software obtained for internal use has generally been enterprise-level business and finance software
that we customize to meet our specific operational needs. Costs incurred in the application development phase are capitalized
and amortized over their useful lives, which is generally five years. Costs recognized in the preliminary project phase and the
post-implementation phase are expensed as incurred. We capitalized $3.9 million and $4.8 million of costs related to the
application development of enterprise-level software that was included in property and equipment during the years ended
December 31, 2014 and December 31, 2013, respectively.

Software development costs

We capitalize software development costs in accordance with ASC 985-20, Costs of Software to Be Sold, Leased, or

Marketed, under which certain software development costs incurred subsequent to the establishment of technological feasibility
may be capitalized and amortized over the estimated lives of the related products. We establish feasibility when we complete a
working model and amortize development costs over the estimated lives of the related products ranging from three to five
years. We capitalized software development costs of $10.4 million and $7.8 million which are included in other assets as of
December 31, 2014 and December 31, 2013, respectively. We recorded $4.4 million, $3.2 million and $2.3 million to cost of
revenues for amortization of capitalized software development costs for the years ended December 31, 2014, December 31,
2013 and December 31, 2012, respectively. All development costs prior to the completion of a working model are recognized as
research and development expense.

Business Combinations

We use the acquisition method of accounting under the authoritative guidance on business combinations. Each
acquired company’s operating results are included in our Consolidated Financial Statements starting on the date of acquisition.
The purchase price is equivalent to the fair value of consideration transferred. Tangible and identifiable intangible assets
acquired and liabilities assumed as of the date of acquisition are recorded at the acquisition date fair value. Goodwill is
recognized for the excess of purchase price over the net fair value of assets acquired and liabilities assumed.

Amounts allocated to assets and liabilities are based upon fair values. Such valuations require management to make

significant estimates and assumptions, especially with respect to the identifiable intangible assets. Management makes
estimates of fair value based upon assumptions believed to be reasonable and that of a market participant. These estimates are
based on historical experience and information obtained from the management of the acquired companies and the estimates are
inherently uncertain. The separately identifiable intangible assets generally include customer relationships, technology, and
trade names.

Goodwill and intangible assets

Goodwill. We review goodwill for impairment on an annual basis on the first day of the fourth quarter of each year at
the reporting unit level. Our reporting units are the same as our operating segments, which are Automation and Analytics and
Medication Adherence. A qualitative assessment is initially made to determine whether it is necessary to perform quantitative
testing. This initial assessment includes, among others, consideration of: (i) past, current and projected future earnings and
equity; (ii) recent trends and market conditions; and (iii) valuation metrics involving similar companies that are publicly-traded

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and acquisitions of similar companies, if available. If this initial qualitative assessment indicates that it is more likely than not
that impairment exists, or if we decide to bypass this option, we proceed to a two-step impairment test. The first step ("Step 1")
involves a comparison between the estimated fair values of our reporting units with their respective carrying amounts including
goodwill. The methods for estimating reporting unit values include asset and liability fair values and other valuation
techniques, such as discounted cash flows and multiples of earnings or revenues. If the carrying value exceeds estimated fair
value, there is an indication of potential impairment, and the second step is performed to measure the amount of impairment.
The second step involves calculating an implied fair value of goodwill by measuring the excess of the estimated fair value of
the reporting units over the aggregate estimated fair values of the individual assets less liabilities. If the carrying value of
goodwill exceeds the implied fair value of goodwill, an impairment charge is recorded for the excess.

To determine each reporting units’ fair value in the second step, we would use the income approach which is based on

the estimated discounted future cash flows of that reporting unit. The estimated fair value of each reporting unit under the
income approach is corroborated with the market approach, which measures the value of a business through an analysis of
recent sales or offerings of a comparable entity. We also consider our market capitalization on the date of the analysis to ensure
the reasonableness of the sum of our reporting units’ estimated fair value.

Intangible assets. In connection with our acquisitions, we generally recognize assets for customer relationships,

technology and trade names. Intangible assets are carried at cost less accumulated amortization. Such amortization is provided
on a straight-line basis or on an accelerated basis based on a pattern of economic benefit that is expected to be obtained over the
estimated useful lives of the respective assets, generally from 1 to 30 years. Amortization for technology is recognized in cost
of product revenues, and amortization for customer relationships and trade names is recognized in selling, general and
administrative expenses.

We assess the impairment of identifiable intangible assets whenever events or changes in circumstances indicate that

an asset's carrying amount may not be recoverable. Recoverability of an asset is measured by the comparison of the carrying
amount to the sum of the undiscounted estimated future cash flows the asset is expected to generate, offset by estimated future
costs to dispose of the product to which the asset relates. If an asset is considered to be impaired, the amount of such
impairment would be measured as the difference between the carrying amount of the asset and its fair value. Our cash flow
assumptions are based on historical and forecasted future revenue, operating costs, and other relevant factors. Assumptions and
estimates about the remaining useful lives of our intangible assets are subjective and are affected by changes to our business
strategies. If management’s estimates of future operating results change, or if there are changes to other assumptions, the
estimate of the fair value of our assets could change significantly. Such change could result in impairment charges in future
periods, which could have a significant impact on our operating results and financial condition.

Valuation of share-based awards

We account for share-based compensation in accordance with ASC 718, Stock Compensation ("ASC 718"). We

recognize compensation expense related to stock-based compensation, including the awarding of employee stock awards and
restricted stock units, based on the grant date estimated fair value. We amortize the fair value of the employee stock awards on
a straight-line basis over the requisite service period of the award, which is generally the vesting period. We estimate the fair
value of stock-based compensation awards using the Black-Scholes option pricing model, which requires the following inputs:
expected life, expected volatility, risk-free interest rate, expected dividend yield rate, exercise price, and closing price of our
common stock on the date of grant. The expected volatility is based on a combination of historical and market-based implied
volatility, and the expected life of the awards is based on our historical experience of employee stock option exercises,
including forfeitures. The valuation assumptions we use in estimating the fair value of employee share-based awards may
change in future periods. We calculate our pool of excess tax benefits available within additional paid-in capital in accordance
with the provisions of ASC 718.

Accounting for income taxes

We record an income tax provision for the anticipated tax consequences of the reported results of operations. In

accordance with U.S. GAAP, the provision for income taxes is computed using the asset and liability method, which requires
the recognition of deferred tax assets and liabilities for the expected future tax consequences of events that have been included
in the financial statements. Under this method, deferred tax assets and liabilities are determined on the basis of the differences

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between the financial statement and tax bases of assets and liabilities and for operating losses and tax credit carry forwards.
Deferred tax assets and liabilities are measured using the enacted tax rates in effect for the periods in which those tax assets and
liabilities are expected to be realized or settled. In the event that these tax rates change, we will incur a benefit or detriment on
our income tax expense in the period of change. If we were to determine that all or part of the net deferred tax assets are not
realizable in the future, we will record a valuation allowance that would be charged to earnings in the period such
determination is made.

In accordance with ASC 740, Income Taxes, we recognize the tax benefit from an uncertain tax position if it is more
likely than not that the tax position will be sustained on examination by the taxing authorities, based on the technical merits of
the position. The tax benefits recognized in the financial statements from such positions are then measured based on the largest
benefit that has a greater than 50% likelihood of being realized upon ultimate settlement. The calculation of tax liabilities
involves significant judgment in estimating the impact of uncertainties in the application of U.S. GAAP and complex tax laws.
Resolution of these uncertainties in a manner inconsistent with management’s expectations could have a material impact on our
financial condition and operating results.

Deferred service revenue and deferred gross profit

Deferred service revenue and deferred gross profit arise when customers have been billed and/or have received

products and/or services in advance of revenue recognition. Our deferred gross profit, classified as a current liability, consists
primarily of unearned revenue on sale of equipment for which installation has not been completed, net of deferred cost of sales
for such equipment and the unearned revenue for software licenses. Our deferred service revenue, separated into current and
long-term liabilities, consists of the unearned portion of service contracts for which revenue is recognized over their duration.

Commissions

Sales commissions are incremental and directly related to customer sales contracts in which revenue is deferred. These

commission costs are accrued and recorded in prepaid expenses upon execution of a non-cancelable customer contract and
subsequently expensed in the period of revenue recognition.

Shipping costs

Outbound freight billed to customers is recorded as product revenue. The related shipping and handling costs are

expensed as part of selling, general and administrative expense. Shipping and handling expenses were $7.4 million, $6.1
million and $4.1 million for the years ended December 31, 2014, December 31, 2013 and December 31, 2012, respectively.

Recently adopted accounting standards

In July 2013, the FASB issued Accounting Standards Update No. 2013-11, Income Taxes: Presentation of an
Unrecognized Tax Benefit When a Net Operating Loss Carryforward, a Similar Tax Loss, or a Tax Credit Carryforward Exists
("ASU 2013-11"). ASU 2013-11 requires an entity to present an unrecognized tax benefit, or a portion of an unrecognized tax
benefit, as a reduction to a deferred tax asset for a net operating loss carryforward, a similar tax loss, or a tax credit
carryforward, except as follows: to the extent a net operating loss carryforward, a similar tax loss, or a tax credit carryforward
is not available at the reporting date under the tax law of the applicable jurisdiction to settle any additional income taxes that
would result from the disallowance of a tax position or the tax law of the applicable jurisdiction does not require the entity to
use, and the entity does not intend to use, the deferred tax asset for such purpose, the unrecognized tax benefit should be
presented in the financial statements as a liability and should not be combined with deferred tax assets. We adopted the
amendments in ASU 2013-11 in the first quarter of 2014. This update did not have a significant impact on our financial
position, operating results or cash flows.

Recently issued authoritative guidance

In May 2014, the FASB issued Accounting Standards Update No. 2014-09, Revenue from Contracts with Customers,
that requires an entity to recognize the amount of revenue to which it expects to be entitled for the transfer of promised goods
or services to customers, and will replace most existing revenue recognition guidance in U.S. GAAP. The new standard is
effective for us in the first quarter of 2017, and early adoption is not permitted. The standard permits the use of either the

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retrospective or cumulative effect transition method. We are evaluating the effect that the standard will have on our
Consolidated Financial Statements and related disclosures.

There was no other recently issued authoritative guidance that has a material impact on our Consolidated Financial

Statements through the reporting date.

Note 2. Business Combinations

2014 Acquisition Activity

On August 22, 2014, we completed our acquisition of Surgichem, a wholly-owned subsidiary of Bupa Care Homes

(CFG) Plc ("Bupa"). In exchange for all of the voting equity interests of the acquired company, we paid a total purchase price
of $20.7 million in cash, net of $0.2 million of cash acquired. This acquisition will assist U.K. healthcare professionals and
caregivers seeking to improve patient outcomes, reduce medication errors and lower costs by effectively managing compliance
to prescribed medication regimes in their mission to extend patient health and satisfaction through convenient, effective
medication adherence solutions. Surgichem is being integrated with Omnicell’s existing U.K. business, MTS, a leading supplier
of medication adherence packaging solutions.

The following table presents the purchase price allocation included in our Consolidated Balance Sheets:

Cash

Accounts receivable

Inventory

Deferred tax assets and other current assets

Total current assets
Property and equipment

Intangibles

Goodwill

Total assets

Current liabilities

Long-term deferred tax liabilities

Total purchase price

(In thousands)
153
2,462
2,190
361
5,166
164
5,730
12,112
23,172
1,191
1,104
20,877

Acquired intangible assets. The fair value of $5.4 million for acquired customer relationships was determined based on

an income approach using the discounted cash flow method. The fair value of $0.3 million for the trade name was determined
using the relief-from-royalty approach. Customer relationships are amortized over their estimated useful lives of 18 years and
the trade name is amortized over its estimated useful life of approximately 1 year.

Goodwill. The purchase price allocation resulted in goodwill of $12.1 million, which represents sales of future

products and services and the assembled workforce of Surgichem. We believe the acquisition enhances Omnicell’s offerings
and diversifies its revenue mix providing a more robust product and service solution to its current customers while expanding
Omnicell’s international presence. We considered these factors as supporting the amount of goodwill recorded.

The amortization of intangible assets and goodwill is not deductible for tax purposes.

We incurred approximately $1.1 million in acquisition-related costs related to the Surgichem acquisition, offset by a

$0.5 million expense reimbursement from Bupa for the year ended December 31, 2014. These costs are included in selling,
general and administrative expenses in our Consolidated Statement of Operations.

Surgichem generated revenue of $4.6 million and losses from operations of $0.1 million since the acquisition date for

the year ended December 31, 2014. The total revenues of Surgichem were $13.3 million (including $4.6 million mentioned
above) and $11.9 million for the years ended December 31, 2014 and December 31, 2013, respectively. Results of operations
for Surgichem have been included as a part of our Medication Adherence segment, and supplemental pro forma results of

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operations for the prior periods have not been presented, as the effect of the acquisition was not material to our consolidated
financial results.

2012 Acquisition Activity

On May 21, 2012, we completed our acquisition of MedPak Holdings, Inc. ("MedPak") pursuant to an Agreement and

Plan of Merger ("Merger Agreement") under which Mercury Acquisition Corp, a newly formed Omnicell subsidiary, was
merged with and into MedPak, with MedPak surviving the merger as a wholly-owned subsidiary of Omnicell. MedPak is the
parent company of MTS, a worldwide provider of medication adherence packaging systems. Pursuant to the terms of the
Merger Agreement, we paid $156.3 million in cash, net of $2.0 million cash acquired.

The objective of the acquisition was to primarily align Omnicell with the long term trends of the healthcare market to
manage the health of patients across the continuum of care. Omnicell and MTS bring capabilities to each other that strengthen
the product lines and expand the medication management coverage of both companies.

The following table presents the purchase price allocation included in our Consolidated Balance Sheets:

Cash

Accounts receivable

Inventory

Deferred tax assets and other current assets

Total current assets
Property and equipment

Intangible assets

Goodwill

Other long-term assets

Total assets

Current liabilities

Long-term deferred tax liabilities

Other long-term liabilities

Total purchase price

(In thousands)
2,000
7,403
11,726
2,894
24,023
9,807
83,900
82,800
308
200,838
(7,917 )

(33,386 )

(1,223 )
158,312

Identifiable intangible assets. Acquired technology relates to MTS’ products across all of its product lines that have

reached technological feasibility, primarily the OnDemand technology. Trade names are primarily related to the MTS and
OnDemand brand names. Customer relationships represent existing contracted relationships with pharmacies, institutional care
facilities and others. Acquired technology, customer relationships, and trade names are amortized on a straight-line basis over
their estimated useful lives, which range from 12 to 30 years.

The estimated fair values of the acquired technology, trade names and customer relationships were primarily
determined using either the relief-from-royalty or excess earnings methods. The interest rates utilized to discount net cash flows
to their present values were determined after consideration of the overall enterprise rate of return and the relative risk and
importance of the assets to the generation of future cash flows.

The historical tax bases of the acquired assets and assumed liabilities, along with the tax attributes of the MTS
companies, will carry over for income tax purposes. As the transaction was a cash-for-stock transaction, there is no tax basis in
the acquired intangible assets. Accordingly, the acquisition accounting includes the establishment of net deferred tax liabilities
of $33.4 million, resulting from book tax basis differences related to the intangible assets acquired, as well as to the step up in
the value of fixed assets and inventory to their estimated fair values at the time of acquisition.

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The following represents the details of the acquired intangible assets:

Trade name

Customer relationships

Acquired technology

Intangibles acquired

Intangible
Assets
Acquired

Useful Life
(Years)

(In thousands, except for years)

6,800
50,500
26,600
83,900

28 to 30

Goodwill. The purchase price allocation resulted in goodwill of $82.8 million. We believe the MTS acquisition

enhances our offerings and diversifies our revenue mix, providing a more robust product and service solution to our current
customers while expanding Omnicell’s international presence. We considered these factors as supporting the amount of
goodwill recorded.

We incurred approximately $3.2 million in acquisition-related costs for the year ended December 31, 2013. These

costs are included in selling, general and administrative expenses in our Consolidated Statement of Operations.

MTS generated revenue of $47.2 million and net income of $2.9 million since the acquisition date for the year ended

December 31, 2012. Results of operations for MTS have been included as a part of our Medication Adherence segment, and
supplemental pro forma results of operations for the prior periods have not been presented, as the effect of the acquisition was
not material to our consolidated financial results.

Note 3. Net Income Per Share

Basic net income per share is computed by dividing net income for the period by the weighted-average number of

shares outstanding during the period, less shares subject to repurchase. Diluted net income per share is computed by dividing
net income for the period by the weighted-average number of shares, less shares subject to repurchase, plus, if dilutive,
potential common stock outstanding during the period. Potential common stock includes the effect of outstanding dilutive stock
options, restricted stock awards and restricted stock units computed using the treasury stock method. Since the impact is anti-
dilutive, these shares were excluded from the calculations of diluted net income per share.

The calculation of basic and diluted net income per share is as follows:

Year Ended

Net income

Weighted-average shares outstanding — basic

Add: Dilutive effect of employee stock plans

Weighted-average shares outstanding — diluted

Net income per share — basic
Net income per share — diluted

Anti-dilutive weighted-average shares related to stock award plans

Note 4. Fair Value Measurements

$
$

December 31,
2012

December 31,
2014

December 31,
2013
(In thousands, except per share data)
30,518 $
35,650
972
36,622

23,979 $
34,736
1,041
35,777

0.86 $
0.83 $
640

0.69 $
0.67 $
850

16,178
33,307
906
34,213
0.49
0.47
2,149

For assets and liabilities measured at fair value, such amounts are based on an expected exit price representing the

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methods were used to estimate the fair value of each class of financial instruments for which it is practical to estimate that
value:

• Level 1: Observable inputs that reflect quoted prices (unadjusted) for identical assets or liabilities in active

markets.

• Level 2: Observable inputs that reflect quoted prices for identical assets or liabilities in markets that are not active,

quoted prices for similar assets or liabilities in active markets, inputs other than quoted prices that are observable
for the assets or liabilities, or inputs that are derived principally from or corroborated by observable market data
by correlation or other means.

• Level 3: Unobservable inputs reflecting our own assumptions incorporated in valuation techniques used to

determine fair value. These assumptions are required to be consistent with market participant assumptions that are
reasonably available.

Assets Measured at Fair Value on a Recurring Basis

Cash equivalents. Cash equivalents consist of money market funds that are classified as Level 1, and have an original

maturity of three months or less, and therefore the carrying amount is a reasonable estimate of fair value due to the short
duration to maturity.

There have been no transfers between fair value measurement levels during 2014 and 2013. The following table

summarizes our assets measured at fair value on a recurring basis using Level 1 inputs within the fair value hierarchy:

Cash

Cash equivalents

Total cash and cash equivalents

December 31,
2014

December 31,
2013

(In thousands)

61,311 $
64,577
125,888 $

38,823
65,708
104,531

Net investment in sales-type leases. The carrying amount of our sales-type lease receivables is a reasonable estimate of

fair value as the unearned interest income is immaterial.

Assets and liabilities measured and recorded at fair value on a nonrecurring basis

See Note 2, Business Combinations, for the fair value of intangible assets acquired that were calculated using an

income approach valuation technique based on Level 3 unobservable inputs.

Note 5. Inventories

Inventories consist of the following components:

Raw materials
Work in process
Finished goods

Total inventories, net

Dependence on suppliers

December 31,
2014

December 31,
2013

(In thousands)
8,254 $
64
23,236
31,554 $

10,765
534
20,158
31,457

We have a supply agreement with one primary supplier for construction and supply of several sub-assemblies and

inventory management of sub-assemblies used in our hardware products. There are no minimum purchase requirements. The
contract with our supplier may be terminated by either the supplier or by us without cause and at any time upon delivery of two

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months' notice. Purchases from this supplier were $34.5 million, $29.2 million and $23.8 million for the years ended
December 31, 2014, December 31, 2013 and December 31, 2012, respectively.

Note 6. Property and Equipment

Property and equipment consist of the following assets:

Equipment

Furniture and fixtures

Leasehold improvements

Purchased software

Construction in progress

Accumulated depreciation and amortization

Total property and equipment, net

December 31,
2014

December 31,
2013

(In thousands)

42,829 $
5,689
8,701
28,920
1,538
87,677
(51,499 )
36,178 $

40,180
5,260
7,394
20,199
2,649
75,682
(40,428 )
35,254

Depreciation and amortization of property and equipment was $11.3 million, $10.9 million and $8.0 million for the

years ended December 31, 2014, December 31, 2013 and December 31, 2012, respectively.

Note 7. Net Investment in Sales-Type Leases

The terms of our sales-type leases are generally up to five years in length. Sales-type lease receivables are

collateralized by the underlying equipment. Net investment in sales-type leases consist of the following components:

Net minimum lease payments to be received

Less: unearned interest income portion

Net investment in sales-type leases
Less: short-term portion

Long-term net investment in sales-type leases

December 31,
2014

December 31,
2013

(In thousands)

17,616 $
(1,131 )
16,485
(5,637 )
10,848 $

18,172
(1,455 )
16,717
(5,232 )
11,485

We evaluate our sales-type leases individually and collectively for impairment, and recorded a collective allowance for

credit losses of $0.2 million and $0.2 million as of December 31, 2014 and December 31, 2013, respectively.

The minimum lease payments under sales-type leases are as follows:

December 31,
2014

2015

2016

2017

2018

2019

Total

Note 8. Goodwill and Intangible Assets

Goodwill

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(In thousands)
6,188
4,832
3,803
2,174
619
17,616

Table of Contents

The changes in the carrying amount of goodwill are as follows:

Net balance as of December 31, 2012

Additions
Adjustments (1)

Net balance as of December 31, 2013
Additions (2)
Adjustments (3)

Net balance as of December 31, 2014
_________________________________________________

Automation and
Analytics

Medication
Adherence

(In thousands)

Total

28,543 $
—
—
28,543 $
—
—
28,543 $

82,864 $
—
(64 )
82,800 $
12,112
(735 )
94,177 $

111,407
—
(64 )
111,343
12,112
(735 )
122,720

(1)

(2)

(3)

Goodwill includes an immaterial adjustment related to the MTS acquisition in May 2012.

Additions to goodwill as a result of the Surgichem acquisition in August 2014, including a $0.1 million adjustment to
the purchase price in the fourth quarter of 2014.

Adjustments reflect foreign currency exchange rate fluctuations.

Effective in the first quarter of 2014, we modified our segment reporting structure to match our new operating
structure. Our reporting units for goodwill are the same as our reportable operating segments. See Note 17, Segment
Information, for information regarding the changes related to segment information.

Intangible assets, net

Customer relationships

Acquired technology

Trade names

Patents

Non-compete agreements
Total intangibles assets, net $ 96,495 $

Gross
Carrying
Amount

Accumulated
Amortization

$ 60,150 $
27,580
7,110
1,655
—

December 31, 2014

December 31, 2013

Net
Carrying
Amount

Useful
Life
(Years)
(In thousands, except for years)
5 - 30

Gross
Carrying
Amount

(7,919 ) $ 52,231
23,512
(4,068 )
5,534
1,390

(1,576 )

(265 )
—

20
— —

3 - 20

1 - 12

$ 54,730 $
27,580
6,890
1,493
60

(13,828 ) $ 82,667

$ 90,753 $

Accumulated
Amortization

Net
Carrying
Amount

Useful
Life
(Years)

(1,003 )

(5,236 ) $ 49,494
(2,598 )

5 - 30
24,982 3 - 20
5,887 3 - 12
1,239
—
(9,151 ) $ 81,602

(254 )

(60 )

We capitalized third-party costs associated with internally-developed patents of $0.3 million, $0.4 million and $0.4

million as of December 31, 2014, December 31, 2013 and December 31, 2012, respectively.

Amortization expense of intangible assets was $4.6 million, $4.3 million and $2.9 million for the years ended

December 31, 2014, December 31, 2013 and December 31, 2012, respectively.

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Total future amortization expense for intangible assets is as follows:

December 31,
2014

2015

2016

2017

2018

2019

Thereafter

Total

Note 9. Other Assets

Other assets consist of the following:

(In thousands)
4,679
4,354
4,267
4,113
4,063
61,191
82,667

Capitalized software development costs, net of accumulated amortization of $14,918 and
$10,547, respectively, and accumulated impairment (1)
Technology license

Long-term deposits
Other long-term assets (2)

Total other long-term assets

_________________________________________________

December 31,
2014

December 31,
2013

(In thousands)

19,643
1,678
860
1,092
23,273 $

13,660
2,350
682
1,245
17,937

(1)

(2)

In the first quarter of 2013, we reorganized our management team as part of the continuing integration of MTS,
including the software development department within the Medication Adherence segment. At this time, $1.8 million
was capitalized as software development costs associated with a software solution that was intended to assist
pharmacies in manual packaging of prescriptions. Our management team reassessed the viability of this project and
the net realizable value of the capitalized costs in light of their decision to change the related product road map and
redesign this product based on evolving market demands. As part of this redesign process, new functionality and
capabilities were needed to be added to the product before commercialization. This redesign was intended to provide a
more robust global platform providing larger scalability and significant functionality not contained in the then-current
beta version. We determined we could no longer support the technological feasibility of this project in conjunction
with our software capitalization policy. Therefore, we abandoned the project and wrote off its net book value of $1.8
million, equating to $0.03 per diluted share, net of tax, which was recorded as an expense of research and development
in our Consolidated Statements of Operations.

Other long-term assets primarily include our equity investments. In the fourth quarter of 2014, we determined our
equity investment accounted for under the cost method of accounting is no longer considered realizable, and therefore
wrote off its net book value of $0.4 million as a non-operating expense in our Consolidated Statements of Operations.

Note 10. Accrued Liabilities

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Accrued liabilities consist of the following:

Rebates and lease buyouts

Advance payments from customers

Group purchasing organization fees

Technology license purchase obligation

Taxes payable

Other accrued liabilities

Total accrued liabilities

Note 11. Deferred Gross Profit

Deferred gross profit consists of the following:

Sales of medication and supply dispensing systems including packaging equipment (1)
Less: cost of revenues, excluding installation costs

Total deferred gross profit

_________________________________________________

(1)

Delivered and invoiced, pending installation.

Note 12. Commitments

Lease commitments

December 31,
2014

December 31,
2013

(In thousands)
6,512 $
4,834
3,475
—
2,181
2,297
19,299 $

1,699
4,971
2,324
1,500
1,664
1,588
13,746

December 31,
2014

December 31,
2013

(In thousands)

36,947 $
(8,389 )
28,558 $

29,040
(9,083 )
19,957

We lease our buildings under operating leases. Commitments under operating leases primarily relate to leasehold

property and office equipment. Rent expense was $6.8 million, $6.9 million and $5.7 million for the years ended December 31,
2014, December 31, 2013 and December 31, 2012, respectively.

The minimum future payments on non-cancelable operating leases are as follows:

December 31,
2014

2015

2016

2017

2018

2019

Thereafter

Total minimum future lease payments

Purchase obligations

(In thousands)
5,637
5,590
4,873
4,711
4,836
12,991
38,638

We purchase components from a variety of suppliers and use contract manufacturers to provide manufacturing

services for our products. During the normal course of business, we issue purchase orders with estimates of our requirements
several months ahead of the delivery dates. These amounts are associated with agreements that are enforceable and legally
binding. Our purchase obligations to our contract manufacturers and suppliers within the next year were $9.3 million as of
December 31, 2014.

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Note 13. Contingencies

Legal Proceedings

On September 12, 2014, MV Circuit Design, Inc., an Ohio company ("MV Circuit"), brought an action to correct the

inventorship of certain patents owned by Omnicell, as well as related state-law claims against Omnicell in the Northern District
of Ohio (Case No. 1:14-cv-02028-DAP) regarding allegations of fraud in the filing and prosecution of U.S. Patent Nos.
8,180,485, 8,773,270, 8,812,153, PCT/US2007/003765, PCT/US2011/063597, and PCT/US2011/0635505 (the “Action”). On
November 14, 2014, we filed a motion to dismiss the Action. MV Circuit Design responded to our motion to dismiss on
January 29, 2015, and we replied in support of our motion to dismiss on February 17, 2015. The court has not yet ruled on the
motion to dismiss. No schedule has yet been set by the court for the case. We intend to defend the matter vigorously.

As required under ASC 450, Contingencies, we accrue for contingencies when we believe that a loss is probable and

that we can reasonably estimate the amount of any such loss. We have not recorded any accrual for contingent liabilities
associated with the legal proceedings described above based on our belief that any potential loss, while reasonably possible, is
not probable. Further, any possible range of loss in these matters cannot be reasonably estimated at this time. We believe that
we have valid defenses with respect to legal proceedings pending against us. However, litigation is inherently unpredictable,
and it is possible that cash flows or results of operations could be materially affected in any particular period by the unfavorable
resolution of this contingency or because of the diversion of management's attention and the creation of significant expenses.

Guarantees

As permitted under Delaware law and our certificate of incorporation and bylaws, we have agreed to indemnify our

directors and officers against certain losses that they may suffer by reason of the fact that such persons are, were or become our
directors or officers. The term of the indemnification period is for the director’s or officer’s lifetime and there is no limit on the
potential amount of future payments that we could be required to make under these indemnification agreements. We have
purchased a directors’ and officers’ liability insurance policy that may enable us to recover a portion of any future payments
that we may be required to make under these indemnification agreements. Assuming the applicability of coverage and the
willingness of the insurer to assume coverage and subject to certain retention, loss limits and other policy provisions, we
believe it is unlikely that we will be required to pay any material amounts pursuant to these indemnification obligations.
However, no assurances can be given that the insurers will not attempt to dispute the validity, applicability or amount of
coverage without expensive and time-consuming litigation against the insurers.

Additionally, we undertake indemnification obligations in our ordinary course of business in connection with, among
other things, the licensing of our products and the provision of our support services. In the ordinary course of our business, we
have in the past and may in the future agree to indemnify another party, generally our business affiliates or customers, against
certain losses suffered or incurred by the indemnified party in connection with various types of claims, which may include,
without limitation, claims of intellectual property infringement, certain tax liabilities, our gross negligence or intentional acts in
the performance of support services and violations of laws. The term of these indemnification obligations is generally
perpetual. In general, we attempt to limit the maximum potential amount of future payments that we may be required to make
under these indemnification obligations to the amounts paid to us by a customer, but in some cases the obligation may not be so
limited. In addition, we have in the past and may in the future warrant to our customers that our products will conform to
functional specifications for a limited period of time following the date of installation (generally not exceeding 30 days) or that
our software media is free from material defects. Sales contracts for certain of our medication packaging systems often include
limited warranties for up to six months, but the periodic activity and ending warranty balances we record have historically been
immaterial.

From time to time, we may also warrant that our professional services will be performed in a good and workmanlike

manner or in a professional manner consistent with industry standards. We generally seek to disclaim most warranties,
including any implied or statutory warranties such as warranties of merchantability, fitness for a particular purpose, title, quality
and non-infringement, as well as any liability with respect to incidental, consequential, special, exemplary, punitive or similar
damages. In some states, such disclaimers may not be enforceable. If necessary, we would provide for the estimated cost of
product and service warranties based on specific warranty claims and claim history. We have not been subject to any significant

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claims for such losses and have not incurred any material costs in defending or settling claims related to these indemnification
obligations. Accordingly, we believe it is unlikely that we will be required to pay any material amounts pursuant to these
indemnification obligations or potential warranty claims and, therefore, no material liabilities have been recorded for such
indemnification obligations as of December 31, 2014 and December 31, 2013.

Note 14. Income Taxes

The following is a geographical breakdown of income before the provision for income taxes:

Domestic

Foreign

Income before provision for income taxes

The provision for income taxes consists of the following:

Current:

Federal

State

Foreign

Total current income taxes

Deferred:

Federal

State

Foreign

Total deferred income taxes

Total provision for income taxes

December 31,
2014

Year Ended

December 31,
2013
(In thousands)

December 31,
2012

48,327 $
177
48,504 $

34,678 $
351
35,029 $

25,794
1,281
27,075

December 31,
2014

Year Ended

December 31,
2013
(In thousands)

December 31,
2012

14,063 $
2,274
192
16,529

1,603
84
(230 )
1,457
17,986 $

8,218 $
1,621
447
10,286

1,287
(263 )

(260 )
764
11,050 $

7,181
1,006
154
8,341

2,169
651
(264 )
2,556
10,897

The provision for income taxes differs from the amount computed by applying the statutory federal tax rate as follows:

U.S. federal tax provision at statutory rate

State taxes

Non-deductible expenses

Acquisition costs

Share-based compensation expense

Research tax credits

Domestic production deduction

Other

Total provision for income taxes

December 31,
2014

Year Ended

December 31,
2013
(In thousands)

December 31,
2012

16,998 $
1,533
809
229
461
(818 )

(1,127 )

(99 )
17,986 $

12,260 $
883
297
—
407
(1,430 )

(816 )

(551 )
11,050 $

9,476
1,077
530
431
403
—
(601 )

(419 )
10,897

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Significant components of our deferred tax assets (liabilities) are as follows:

Deferred tax assets (liabilities):

Deferred revenue

Stock compensation

Inventory related items

Tax credit carry forwards

Reserves and accruals

Loss carry forwards

Other, net

Subtotal

Less: valuation allowance

Total net deferred tax assets

Intangibles

Depreciation and amortization

Reserves and accruals

Other, net

Total deferred tax liabilities

December 31,
2014

December 31,
2013

(In thousands)

12,639 $
6,287
2,713
2,168
327
12
—
24,146
—
24,146

(26,485 )

(14,331 )
—
(194 )

(41,010 )

11,074
7,447
2,947
3,160
—
64
5
24,697
(39 )
24,658

(26,604 )

(12,077 )

(353 )
—

(39,034 )

Net deferred tax liabilities

(16,864 ) $

(14,376 )

Deferred income tax assets (liabilities) are provided for temporary differences that will result in future tax deductions

or future taxable income, as well as the future benefit of tax credit carry forwards. We recognize deferred tax assets to the
extent that we believe these assets are more likely than not to be realized. In making such a determination, we consider all
available positive and negative evidence, including future reversals of existing temporary differences, projected future taxable
income, tax planning strategies, and results of recent operations. On the basis of this evaluation, as of December 31, 2014, no
valuation allowances have been recorded in any jurisdiction.

As of December 31, 2014, we have an immaterial amount of state net operating loss carryforwards available for

income tax purposes. For income tax purposes, we have California research tax credits carryforwards of $7.9 million. Federal
research tax credit carryforwards from prior years have been utilized or have expired. California credits are available
indefinitely to reduce cash taxes otherwise payable. Pursuant to the requirements of ASC 718, we do not include unrealized
stock option attributes as components of our gross deferred tax assets. The tax-effected amounts of gross unrealized net
operating loss and business tax credit carryforwards excluded under ASC 718 for the year ended December 31, 2014 are
immaterial.

In general, it is the practice and intention to reinvest the earnings of our non-U.S. subsidiaries in those operations. As

of December 31, 2014, we have not made a provision for U.S. federal income and state income taxes on accumulated and
current earnings of $0.8 million related to our foreign subsidiaries because these earnings are intended to be indefinitely
reinvested in operations outside the United States. If we expect to distribute those earnings in the form of dividends or
otherwise, we would be subject to U.S. and state income taxes reported as a component of income tax expense, in the amount
of $0.3 million. This amount may be reduced by any foreign tax credits available at the time of repatriation.

We file income tax returns in the United States and various states and foreign jurisdictions. In the normal course of

business, we are subject to examination by taxing authorities, including major jurisdiction as the United States, California and
United Kingdom and Germany. In 2012, we concluded audits by IRS and California Franchise Tax Board for years 2008 and
2009. However, all of the net operating loss and research credit carryforwards that may be used in future years are subject to

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adjustment, if and when utilized. As such our federal and California tax years remain open from 1996 and 1992, respectively. In
late 2014, we were contacted by the IRS for a limited scope audit for tax years 2011 and 2012. At this time, we do not believe
results of this audit will have a material impact on our financial statements.

The aggregate change in the balance of gross unrecognized tax benefits, which excludes interest and penalties, is as

follows:

Year Ended December 31, 2011

Increases related to tax positions taken during a prior period

Increases related to tax positions related to MTS

Decreases related to tax positions taken during the prior period

Increases related to tax positions taken during the current period

Decreases related to settlements

Decreases related to expiration of statute of limitations

Year Ended December 31, 2012

Increases related to tax positions taken during a prior period

Decreases related to tax positions taken during the prior period

Increases related to tax positions taken during the current period

Decreases related to settlements

Decreases related to expiration of statute of limitations

Year Ended December 31, 2013

Increases related to tax positions taken during a prior period

Decreases related to tax positions taken during the prior period

Increases related to tax positions taken during the current period

Decreases related to settlements

Decreases related to expiration of statute of limitations

Year Ended December 31, 2014

(In thousands)
5,796
43
1,066
—
422
(33 )

(379 )
6,915
406
(79 )
764
—
(32 )
7,974
63
(89 )
801
—
(264 )
8,485

As of December 31, 2014, the total amount of gross unrecognized tax benefits, if realized, would affect our tax

expense by approximately $7.3 million. We recognize interest and/or penalties related to uncertain tax positions in operating
expenses, which for 2014 was immaterial. We do not believe there will be any material changes in our unrecognized tax
positions over the next twelve months.

Note 15. Stock Repurchases

The following table summarizes our stock repurchases:

Year Ended

December 31,
2014

December 31,
2013
(In thousands, except per share data)

December 31,
2012

Total number of shares repurchased

Dollar amount of shares repurchased

Average price paid per share

884
24,091 $
27.24 $

885
20,962 $
23.70 $

898
12,363
13.76

In August 2012, our Board of Directors authorized a program to repurchase up to $50.0 million of common stock, of

which approximately $45.1 million had been repurchased as of December 31, 2014. In November 2014, our Board of Directors
authorized a program to repurchase up to $50.0 million of common stock. We expect to begin repurchasing shares under the
2014 Stock Repurchase Program upon the completion of the 2012 Stock Repurchase Program. Our stock repurchase programs

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have a total of $54.9 million remaining for future repurchases as of December 31, 2014, and neither program has an expiration
date.

Note 16. Employee Benefits and Share-Based Compensation

Stock purchase plan

1997 Employee Stock Purchase Plan

We have an Employee Stock Purchase Plan ("ESPP"), under which employees can purchase shares of our common
stock based on a percentage of their compensation, but not greater than 15% of their earnings; provided, however, an eligible
employees' right to purchase shares of our common stock may not accrue at a rate which exceeds $25,000 of the fair market
value of such shares for each calendar year in which such rights are outstanding. The purchase price per share must be equal to
the lower of 85% of the fair value of the common stock at the beginning of a 24-month offering period or the end of each six-
month purchasing period.

At our 2009 Annual Meeting of Stockholders ("2009 Annual Meeting"), the stockholders approved an amendment to

the ESPP, which added 2.6 million shares to the reserve for future issuance. There was a total of 0.6 million shares reserved for
future issuance under the ESPP as of December 31, 2014. For the year ended December 31, 2014, 0.5 million shares of
common stock were purchased under the ESPP and an aggregate of 4.7 million shares were issued under the ESPP as of
December 31, 2014.

The unrecognized compensation cost related to the shares to be purchased under our ESPP was approximately $1.8

million, and is expected to be recognized over a weighted-average period of 0.7 years as of December 31, 2014.

Stock award plans

2009 Equity Incentive Plan

On May 19, 2009, at our 2009 Annual Meeting, our stockholders approved the Omnicell, Inc. 2009 Equity Incentive

Plan ("2009 Plan") which authorized 2.1 million shares to be issued. The 2009 Plan provides for the issuance of incentive stock
options, non-statutory stock options, stock appreciation rights, restricted stock awards, restricted stock unit awards,
performance stock awards, performance cash awards and other stock awards to our employees, directors and consultants.

The 2009 Plan succeeded the 1999 Equity Incentive Plan, the 2003 Equity Incentive Plan and the 2004 Equity
Incentive Plan (collectively, the "Prior Plans"). No additional awards will be granted under any of the Prior Plans; however, all
outstanding stock awards granted under the Prior Plans continue to be subject to the terms and conditions as set forth in the
agreements evidencing such stock awards. For purposes of determining future common shares available for grant, for each
share granted as a full-value award, including restricted stock awards ("RSAs"), restricted stock unit awards ("RSUs") and
performance stock awards, the shares available for issuance were reduced by 1.4 shares for each share granted. Equity awards
granted as options and stock appreciation rights reduce the shares available for issuance by one share.

On December 16, 2010, at a Special Meeting of Stockholders, our stockholders approved an amendment to increase
the number of shares of common stock authorized for issuance under the 2009 Plan by 2.6 million shares and to provide that
the number of common stock shares available for issuance under the 2009 Plan be reduced by 1.8 shares for each share granted
as a full-value award granted on and after October 1, 2010. For each share granted as a full-value award granted prior to
October 1, 2010, future shares available for grants under the 2009 Plan were reduced by 1.4 shares. Awards granted as stock
options and stock appreciation rights continue to reduce the number of shares available for issuance under the 2009 Plan on a
one-for-one basis. At our 2013 Annual Meeting of Stockholders, our stockholders approved an amendment to the 2009 Plan to
increase the number of shares of common stock authorized for issuance by 2.5 million shares. There were 1.8 million shares of
common stock reserved for future issuance under the 2009 Plan as of December 31, 2014.

Options granted under the 2009 Plan generally become exercisable over periods of up to 4 years, generally with one-

fourth of the shares vesting one year from the vesting commencement date with respect to initial grants, and the remaining
shares vesting in 36 equal monthly installments thereafter; however our Board of Directors may impose different vesting terms
at its discretion on any award. Options under the 2009 Plan generally expire 10 years from the date of grant. We also grant both
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restricted stock and restricted stock units to participants under the 2009 Plan. The Board of Directors determines the award
amount, the vesting provisions and the expiration period (not to exceed ten years) for each grant. Grants of restricted stock to
non-employee directors are granted on the date of our annual meeting of stockholders and vest in full on the date of our next
annual meeting of stockholders, provided such non-employee director remains a director on such date. The fair value of the
stock on the date of issuance is amortized to expense from the date of grant to the date of vesting. RSUs granted to employees
generally vest over a period of four years and are expensed ratably on a straight-line basis over the vesting period. We consider
the dilutive impact of options, restricted stock and restricted stock units in our diluted net income per share calculation.

The 2009 Plan provides that our Board of Directors shall administer the 2009 Plan unless and until the Board of

Directors delegates administration to a committee. Our Board of Directors has delegated administration of the 2009 Plan to the
Compensation Committee of the Board and the 2009 Plan is generally administered by such committee. The Board of Directors
may suspend or terminate the 2009 Plan at any time. The Board of Directors may also amend the 2009 Plan at any time or from
time to time. However, no amendment will be effective unless approved by our stockholders after its adoption by the Board of
Directors to the extent stockholder approval is necessary to satisfy the applicable listing requirements of NASDAQ.

Performance-based restricted stock units

In 2011, we began incorporating performance-based restricted stock units ("PSUs") as an element of our executive
compensation plans. In 2012, we granted 125,000 PSUs to our executive officers, of which 62,500 PSUs became eligible for
vesting upon the achievement of a certain level of shareholder return for 2012. In 2013, we granted 137,500 PSUs to our
executive officers all of which became eligible for vesting upon the achievement of a certain level of shareholder return for the
period from January 1, 2013 through February 28, 2014. In 2014, we granted 132,500 PSUs to our executive officers, all, none
or a portion of which may become eligible for vesting depending on the level of shareholder return for 2014 and eligible for
further time-based vesting based on the ranking of our total shareholder return.

The fair value of a PSU award is the average of trial-specific values of the award over each of one million Monte

Carlo trials. Each trial-specific value is the market value of the award at the end of the one-year performance period discounted
back to the grant date. The market value of the award for each trial at the end of the performance period is the product of (a) the
per share value of Omnicell stock at the end of the performance period and (b) the number of shares that vest. The number of
shares that vest at the end of the performance period depends on the percentile ranking of the total shareholder return for
Omnicell stock over the performance period relative to the total shareholder return of each of the other companies in the
NASDAQ Healthcare Index (the "Index").

Vesting for the PSUs is based both on the percentile placement of our total stockholder return among the companies

listed in the Index and time-based vesting. We calculate total stockholder return based on the one year annualized rates of
return reflecting price appreciation plus reinvestment of dividends. For PSUs granted on February 4, 2014, stock price
appreciation is calculated based on the trailing 20-day average stock price from the first trading day of March 2014, compared
to the trailing 20-day average stock price from the first trading day of March 2015. For PSUs granted in 2013, stock price
appreciation is calculated based on the average closing prices of the applicable company’s common stock for the 20 trading
days ended on the last trading day of 2012 as compared to the average closing prices of the common stock for the 20 trading
days preceding the first trading day of March 2014. For PSUs granted in 2012, stock price appreciation is calculated based on
the average closing prices of the applicable company's common stock for the 20 trading days ending on the last trading day of
2011 as compared to the average closing prices for the 20 trading days ended on the last trading day of 2012.

On January 17, 2012, the Compensation Committee confirmed 76.3% as the percentile rank of our 2011 total

stockholder return. This resulted in 120% of the 2011 PSUs, or 120,000 shares, becoming eligible for further time-based
vesting. The eligible PSUs vest as follows: 25% of the eligible awards for the first year vested on January 17, 2012 with the
remaining eligible awards vesting in equal increments, semi-annually, over the subsequent three-year period beginning on June
15th and December 15th of the year after the date of grant and each subsequent year. Vesting is contingent upon continued
service. Of the 120,000 shares eligible for time-based vesting under the 2011 PSUs, 30,000 shares vested during the year ended
December 31, 2014.

On January 22, 2013, the Compensation Committee confirmed 35.3% as the percentile rank of our 2012 total

stockholder return. This resulted in 50% of the 2012 PSUs, or 62,500 shares, as eligible for further time-based vesting. The

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eligible PSUs vest as follows: 25% of the eligible shares vested immediately on January 22, 2013 with the remaining eligible
awards vesting in equal increments, semi-annually, over the subsequent three-year period beginning on June 15th and
December 15th of the year after the date of grant and each subsequent year. Vesting is contingent upon continued service. Of
the 62,500 shares eligible for time-based vesting under the 2012 PSUs, 15,600 shares vested during the year ended
December 31, 2014.

On March 20, 2014, the Compensation Committee confirmed 63.9% as the percentile rank of our 2013 total
stockholder return. This resulted in 100% of the 2013 PSUs, or 137,500 shares, as eligible for further time-based vesting. The
eligible performance based restricted stock unit awards will vest as follows: 25% of the eligible shares vested immediately on
March 20, 2014 with the remaining eligible awards vesting in equal increments, semi-annually, over the subsequent three-year
period beginning on June 15th and December 15th of the year after the date of grant and each subsequent year. Vesting is
contingent upon continued service. Of the 137,500 shares eligible for time-based vesting under the 2013 PSUs, 68,750 shares
vested during the year ended December 31, 2014.

On February 5, 2014, the Compensation Committee approved PSUs of 132,500 shares. If the minimum performance
threshold is met as determined by the Compensation Committee in 2015, the eligible performance-based restricted stock unit
awards will vest as follows: 25% of the eligible shares will vest immediately, with the remaining eligible awards vesting in
equal increments, semi-annually, over the subsequent three year period beginning on June 15th and December 15th of the year
after the date of grant and each subsequent year. Vesting is contingent upon continued service.

Valuation of share-based awards

The fair value of each option grant is estimated on the date of grant using the Black-Scholes-Merton option-pricing
model. The fair value of shares issued under the employee stock purchase plans is estimated on the date of issuance using the
Black-Scholes-Merton model.

The following assumptions were used to estimate the fair value of share-based awards:

Stock Option Plans
Risk-free interest rate (1)
Dividend yield
Expected volatility (2)
Expected life (3)

Employee Stock Purchase Plan
Risk-free interest rate (1)
Dividend yield
Expected volatility (2)
Expected life (3)
_________________________________________________

Year Ended

December 31,
2014

December 31,
2013

December 31,
2012

1.6 %

— %

34.9 %

1.2 %

— %

43.1 %

0.9 %

— %

45.8 %

4.8 years

5.3 years

5.2 years

Year Ended

December 31,
2014

December 31,
2013

December 31,
2012

0.2 %

— %

33.2 %

0.2 %

— %

35.1 %

0.2 %

— %

38.5 %

0.5 - 2 years

(1)

(2)

The risk-free interest rate for both stock options and the ESPP is based on the zero-coupon U.S. Treasury rate curve in
effect at the time of the option grant or at the beginning of the ESPP offering period.

Expected volatility for both stock options and the ESPP reflects a combination of historical and market-based implied
volatility consistent with ASC 718 and SEC Staff Accounting Bulletin 107. We determined that the combination of
historical and market-based implied volatility provides a more accurate reflection of our market conditions and is more
representative of future stock price trends than employing solely historical volatility.

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(3)

Represents the period of time that options granted are expected to be outstanding, which is derived from historical data
on employee exercise and post-vesting employment termination behavior.

Share-based compensation expense

We account for share-based awards granted to employees and directors, including employee stock option awards,

restricted stock, PSUs and RSUs issued pursuant to the 2009 Plan and employee stock purchases made under our ESPP using
the estimate grant date fair value method of accounting in accordance with ASC 718, Stock Compensation. We value options
and ESPP shares using the Black-Scholes-Merton option-pricing model. Restricted stock and time-based RSUs are valued at
the grant date fair value of the underlying common shares. The PSUs are valued using the Monte Carlo simulation model.

The following table sets forth the total share-based compensation expense recognized in our Consolidated Statements

of Income:

Cost of product and service revenues

Research and development

Selling, general and administrative

Total share-based compensation expense

December 31,
2014

Year Ended

December 31,
2013
(In thousands)

December 31,
2012

1,456 $
1,655
9,674
12,785 $

1,241 $
1,359
8,551
11,151 $

1,011
889
7,314
9,214

We did not capitalize any share-based compensation as inventory as such amounts were not material for the years

ended December 31, 2014, December 31, 2013 and December 31, 2012. Income tax benefits realized from share-based
compensation were $4.5 million, $2.4 million and $2.6 million, for the years ended December 31, 2014, December 31, 2013
and December 31, 2012, respectively.

Stock options activity

A summary of the stock option activity under the 2009 Plan is presented below:

Outstanding at December 31, 2013

Granted

Exercised

Expired

Forfeited

Outstanding at December 31, 2014

Exercisable at December 31, 2014
Vested and expected to vest at December 31, 2014
_________________________________________________

Number of
Shares

Weighted-
Average
Exercise Price

Weighted-
Average
Remaining
Years

Aggregate
Intrinsic Value(1)

(In thousands, except per share data)

3,143 $
641
(1,007 )

(12 )

(93 )
2,672 $
1,514 $
2,640 $

15.82
28.11
14.74
19.88
19.97
19.02
15.66
18.92

5.6

6.5 $

4.7 $
6.4 $

37,692
26,447
37,481

(1)

Intrinsic value is calculated as the difference between the market value or closing price of our common stock as of the
last trading day of the year as reported by the NASDAQ Global Select Market, and the exercise price of the option.

The weighted-average fair value per share of options granted during 2014, 2013 and 2012 was $9.12, $8.09 and $6.13,

respectively. The intrinsic value of options exercised during 2014, 2013 and 2012 was $14.1 million, $14.0 million and $2.8
million, respectively.

As of December 31, 2014, total unrecognized compensation cost related to unvested stock options was $8.8 million,

which is expected to be recognized over a weighted-average vesting period of 2.8 years.

F-32

Table of Contents

Restricted stock activity

A summary of the restricted stock activity under the 2009 Plan is presented below:

Restricted Stock Units

Outstanding at December 31, 2013

Granted

Vested

Forfeited

Outstanding and unvested at December 31, 2014

Expected to vest at December 31, 2014

Number of
Shares

Weighted-
Average
Grant Date Fair
Value

Weighted-
Average
Remaining
Years

(In thousands, except per share data)

Aggregate
Intrinsic Value

362 $
238
(181 )

(20 )
399 $
387

17.15
28.88
17.51
16.50
24.00

2.5

1.5 $

13,190
12,807

The weighted-average grant date fair value per share of RSUs granted during 2014, 2013 and 2012 was $28.88, $19.87

and $14.58, respectively. The total fair value of RSUs that vested in 2014, 2013 and 2012 was $3.2 million, $4.4 million and
$2.3 million, respectively.

As of December 31, 2014, total unrecognized compensation cost related to RSUs was $8.7 million, which is expected

to be recognized over the remaining weighted-average vesting period of 2.6 years.

Restricted Stock Awards

Outstanding at December 31, 2013

Granted

Vested

Forfeited

Outstanding and unvested at December 31, 2014

Number of
Shares

Weighted-
Average
Grant Date Fair
Value

(In thousands, except per share data)

52 $
38
(54 )
—
36 $

18.43
26.42
18.68
—
26.47

The weighted-average grant date fair value per share of RSAs granted during 2014, 2013 and 2012 was $26.42, $18.20

and $14.19, respectively. The total fair value of RSAs that vested in 2014, 2013 and 2012 was $1.0 million, $1.1 million and
$1.1 million, respectively.

As of December 31, 2014, total unrecognized compensation cost related to RSAs was $0.4 million, which is expected

to be recognized over the remaining weighted-average vesting period of 0.5 years.

Performance-based restricted stock units activity

A summary of the performance-based restricted stock activity under the 2009 Plan is presented below:

Unvested at December 31, 2013

Granted

Vested

Cancelled

Unvested at December 31, 2014

F-33

Number of
Shares

Weighted-
Average
Grant Date Fair
Value Per Unit
(In thousands, except per share data)
13.32
20.94
13.32
16.73
17.96

225 $
158
(114 )

(36 )
233 $

Table of Contents

The weighted-average grant date fair value per share of PSUs granted during 2014, 2013 and 2012 was $20.94, $14.68

and $10.94, respectively. The total fair value of PSUs that vested in 2014, 2013 and 2012 was $1.5 million, $0.7 million and
$0.7 million, respectively.

As of December 31, 2014, total unrecognized compensation cost related to PSUs was approximately $2.0 million,

which is expected to be recognized over the remaining weighted-average period of 1.2 years.

401(k) Plan

We have established a 401(k) tax-deferred savings plan ("Omnicell Plan"), whereby eligible employees may contribute

a percentage of their eligible compensation, but not greater than 75% of their earnings, up to the maximum as required by law.
On January 1, 2009, we began matching 401(k) contributions, up to a maximum of 3% of employee contributions, not to
exceed $1,000 for the year. In the first quarter of 2013, the MTS 401(k) tax-deferred savings plan was merged with the
Omnicell Plan. On January 1, 2014, the Omnicell Plan was changed to match 50% of employee contributions up to $1,500,
with no limit to employee contributions as long as such contributions do not exceed 75% of their earnings. Effective January 1,
2015, we will begin to match 50% of employee contributions up to $2,000, with the same limitations on employee
contributions as of January 1, 2014.

Our contributions under the Omnicell Plan were $1.3 million, $1.1 million and $0.8 million in 2014, 2013 and 2012,

respectively.

Preferred Stock

There were 5.0 million preferred shares authorized, and no preferred shares issued or outstanding as of December 31,

2014 and December 31, 2013.

Note 17. Segment Information

In the first quarter of 2014, we began to manage our business according to two product segments because many of our
Acute Care and Non-Acute Care customers were converging to provide services across the continuum of care. We modified our
segment reporting structure to match our operating structure based on how our CODM views the business and allocates resources.
The two operating segments, which are the same as our reporting segments, are as follows:

Automation and Analytics

The Automation and Analytics segment is organized around the design, manufacturing, selling and servicing of
medication and supply dispensing systems, pharmacy inventory management systems, and related software. Our Automation and
Analytics products are designed to enable our customers to enhance and improve the effectiveness of the medication-use process,
the efficiency of the medical-surgical supply chain, overall patient care and clinical and financial outcomes of medical facilities.
Through modular configuration and upgrades, our systems can be tailored to specific customer needs.

Medication Adherence

The Medication Adherence segment includes primarily the manufacturing and selling of consumable medication blister

cards, packaging equipment and ancillary products and services. These products are used to manage medication administration
outside of the hospital setting and include medication adherence products sold under the brand name of MTS, Surgichem, and
under the Omnicell brand, and dispensing systems sold under the Omnicell brand. MTS products consist of proprietary medication
packaging systems and related products for use by institutional pharmacies servicing long-term care, and correctional facilities or
retail pharmacies serving patients in their local communities.

The historical information presented has been retrospectively adjusted to reflect the new segment reporting. Our CODM
allocates resources and evaluates the performance of our segments using information about its revenues, gross profit and income
from operations. Except for goodwill, as discussed in Note 8, our assets are not discretely identified or allocated by segment.

F-34

Table of Contents

The following table summarizes the financial performance of our reporting segments:

December 31, 2014

Year Ended

December 31, 2013

December 31, 2012

Automation
and
Analytics

Medication
Adherence
(1)

Total

Automation
and
Analytics

Medication
Adherence

Total

Automation
and
Analytics

Medication
Adherence
(2)

Total

(In thousands)

Revenues

Gross profit

Cost of revenues

86,805 $ 440,900 $ 302,917 $
129,314
207,040
55,713
173,603
233,860
31,092
140,087
184,277
29,121
33,516 $
49,583 $
1,971 $
_________________________________________________

$ 354,095 $
151,327
202,768
155,156
47,612 $

Income from operations $

Operating expenses

77,668 $ 380,585 $ 260,160 $
111,599
177,186
47,872
148,561
203,399
29,796
127,467
168,100
28,013
21,094 $
35,299 $
1,783 $

53,867 $ 314,027
143,439
31,840
170,588
22,027
143,462
15,995
27,126
6,032 $

(1)

(2)

Includes Surgichem results as of August 2014.
Includes MTS results as of May 2012.

Geographical Information

United States
Foreign countries (1)

Total revenues

December 31,
2014

394,234
46,666
440,900

Year Ended

December 31,
2013
(In thousands)
334,412
46,173
380,585

December 31,
2012

287,716
26,311
314,027

_________________________________________________

(1)

No individual country represented more than 10% of the respective totals.

Significant customers

There were no significant customers that accounted for more than 10% of our total revenues in 2014, 2013 and 2012.

Note 18. Credit Agreement

In September 2013, we entered into a credit agreement (the "Credit Agreement") with Wells Fargo Bank, National

Association, as administrative agent, and the lenders from time to time party thereto. The Credit Agreement provides for a $75
million revolving credit facility with a $10 million letter of credit sub-limit. Loans under the Credit Agreement mature on
September 25, 2018. The Credit Agreement permits us to request one or more increases in the aggregate commitments provided
that such increases do not exceed $25 million in the aggregate. We expect to use the proceeds from any revolving loans under
the credit facility for general corporate purposes, including future acquisitions. Our obligations under the Credit Agreement are
guaranteed by certain of our domestic subsidiaries and secured by substantially all of our and the subsidiary guarantors’ assets.
We have not yet drawn any funds under the credit facility to date.

Amounts drawn under the Credit Agreement bear interest, at our election, at a Eurodollar rate plus a margin of 1.75%

per annum, or an alternate base rate equal to the highest of (i) the prime rate, (ii) the federal funds rate plus 0.50%, and (iii)
LIBOR for an interest period of one month plus 1.75%. We are required to pay a commitment fee of 0.25% per annum on the
aggregate undrawn amount of the commitments under the credit facility.

On November 5, 2014, we entered into Amendment Number One (“Amendment”) to the Credit Agreement. The
Amendment increases the amount of our common stock that may be repurchased by us in open market transactions authorized
by our Board of Directors, together with any repurchases of our common stock from any consultants, employees, officers or
directors of the Company or any of our subsidiaries following the death, disability, retirement or termination of employment of
such employees, officers or directors, from $25 million to $50 million per year.

F-35

Table of Contents

The Credit Agreement contains customary affirmative and negative covenants, including, among other things,
restrictions on indebtedness, liens, investments, mergers, dispositions, dividends and other distributions. The Credit Agreement
contains financial covenants that require us to, among other things, maintain a maximum consolidated total leverage ratio and a
minimum consolidated fixed charge coverage ratio, in each case, as of the last day of each quarter. We were in full compliance
with all covenants as of December 31, 2014.

Note 19. Subsequent Events

On February 26, 2015, Omnicell International, Inc., a wholly-owned subsidiary of Omnicell, Inc. entered into an

agreement with Apotheka Imedisa 2001 S.A., Holger Wallat, Dirk Rolf Beils and Peter Jansen (collectively, the “Selling
Shareholders”) for the purchase of the entire registered share capital of Mach 4 Automatisierungstechnik GmbH (“Mach4”)
(the “Share Purchase Agreement”). Mach4 is a provider of automated medication management systems to retail and hospital
pharmacy customers primarily in Europe, with additional installations in China, the Middle East and Latin America. The
contemplated total aggregate consideration is $18.0 million in cash, minus existing debt and subject to certain adjustments
provided for in the Share Purchase Agreement. The closing of the acquisition is subject to certain closing conditions.

On February 27, 2015, the Company received a notice from an Omnicell employee alleging, among other matters, the
existence of a "side letter" arrangement with an Omnicell customer for certain discounts and Omnicell products that were to be
provided at no cost, but which were not reflected in the final invoices paid by the customer. Following the receipt of this notice,
the Company commenced an internal investigation into these allegations. This investigation was concluded on March 25, 2015.
Based on the results of the investigation, the Company has determined that effective internal control over financial reporting
was maintained in all material respects and that there are no changes required to be made to the Company’s Consolidated
Financial Statements.

F-36

Table of Contents

SCHEDULE II

VALUATION AND QUALIFYING ACCOUNTS

Additions

Balance at
Beginning of
Period (1)

Charged to
Costs and
Expenses (2)

Credited to
Other Accounts
(3)
(In thousands)

Amount
Written Off (4)

Balance at
End of Period (1)

Year ended December 31, 2012

Accounts receivable

Investment in sales-type leases

Total allowances deducted from assets

Year ended December 31, 2013
Accounts receivable

Investment in sales-type leases

Total allowances deducted from assets

Year ended December 31, 2014
Accounts receivable

Investment in sales-type leases

Total allowances deducted from assets

__________________________________________________

443 $
284
727 $

722 $
607
1,329 $

490 $
167
657 $

(1)
(2)
(3)
(4)

Allowance for doubtful accounts.
Represents amounts charged to bad debt expense.
Represents amounts credited to bad debt expense.
Represents amounts written-off, net of recoveries.

316 $
425
741 $

195 $
49
244 $

941 $
—
941 $

(57 ) $
—

(57 ) $

(67 ) $
—

(67 ) $

(60 ) $

(5 )

(65 ) $

20 $

(102 )

(82 ) $

(360 ) $

(489 )

(849 ) $

(165 ) $
—
(165 ) $

722
607
1,329

490
167
657

1,206
162
1,368

F-37

Table of Contents

Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly
caused this report to be signed on its behalf by the undersigned, thereunto duly authorized on the 30th day of March, 2015.

SIGNATURES

OMNICELL, INC.
By:

/s/ ROBIN G. SEIM

Robin G. Seim,
Chief Financial Officer and Executive Vice President
Finance, International and Manufacturing

POWER OF ATTORNEY

KNOW ALL PERSONS BY THESE PRESENTS, that each of the persons whose signature appears below hereby

constitutes and appoints Randall A. Lipps and Robin G. Seim, each of them acting individually, as his or her attorney-in-fact,
each with the full power of substitution, for him or her in any and all capacities, to sign any and all amendments to this Annual
Report on Form 10-K, and to file the same, with all exhibits thereto and other documents in connection therewith, with the
Securities and Exchange Commission, granting unto said attorneys-in-fact, and each of them, 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 or she might or could do in person, hereby ratifying and confirming our signatures as they may be signed
by our said attorney-in-fact and any and all amendments to this Annual Report on Form 10-K.

Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the

following persons on behalf of the registrant and in the capacities and on the dates indicated.

Signature

/s/ RANDALL A. LIPPS

Randall A. Lipps

/s/ ROBIN G. SEIM

Robin G. Seim

/s/ JOANNE B. BAUER

Joanne B. Bauer

/s/ JAMES T. JUDSON

James T. Judson

/s/ RANDY D. LINDHOLM

Randy D. Lindholm

/s/ VANCE B. MOORE

Vance B. Moore

/s/ MARK W. PARRISH

Mark W. Parrish

/s/ GARY S. PETERSMEYER

Gary S. Petersmeyer

/s/ BRUCE D. SMITH

Bruce D. Smith

Sara J. White

Title

Chief Executive Officer, President and Chairman of the Board
(Principal Executive Officer)

Chief Financial Officer and Executive Vice President Finance,
International and Manufacturing
(Principal Accounting and Financial Officer)

Director

S- 1

Date

March 30, 2015

Table of Contents

INDEX TO EXHIBITS

Exhibit
Number

2.1

3.1

3.2

3.3

3.4

4.1

4.2

Exhibit Description

Form

File No.

Exhibit

Filing Date

Incorporated By Reference

Agreement for the sale and purchase of the entire issued share
capital of Surgichem Limited, by and among Omnicell, Inc.,
BUPA Care Homes (CFG) Plc, and MTS Medication
Technologies, Inc.
Amended and Restated Certificate of Incorporation of
Omnicell, Inc.

Certificate of Amendment to the Amended and Restated
Certificate of Incorporation of Omnicell, Inc.

Certificate of Designation of Series A Junior Participating
Preferred Stock

8-K

000-33043

2.1

12/9/2013

S-1

333-57024

3.1

3/14/2001

10-Q

000-33043

3.2

8/9/2010

10-K

000-33043

3.2

3/28/2003

Bylaws of Omnicell, Inc., as amended

10-Q

000-33043

3.3

8/9/2007

Reference is made to Exhibits 3.1, 3.2, 3.3 and 3.4

Form of Common Stock Certificate

S-1

333-57024

4.1

3/14/2001

10.1*

2013 Executive Officer Annual Base Salaries

8-K

000-33043

10.1

2/7/2013

10.2*

2014 Executive Officer Annual Base Salaries

8-K

000-33043

10.1

2/7/2014

10.3

10.4

10.5

10.6

Lease, effective July 1, 1999, between AMLI Commercial
Properties Limited Partnership and Omnicell, Inc.

First Amendment to Lease, dated September 30, 1999, between
AMLI Commercial Properties Limited Partnership and
Omnicell, Inc.

Lease, dated April 14, 2010, between Point Place II, LLC and
Omnicell, Inc.

Lease Agreement, dated October 20, 2011, between
Middlefield Station Associates, LLC and Omnicell, Inc.

S-1

333-57024

10.2

3/14/2001

10-K

000-33043

10.6

3/8/2012

10-K

000-33043 10.10

3/11/2011

10-K

000-33043

10.9

3/8/2012

10.7

Form of Director and Officer Indemnity Agreement

S-1

333-57024 10.12

3/14/2001

10.8*

1997 Employee Stock Purchase Plan, as amended

10-Q

000-33043

10.2

8/5/2009

10.9*

2003 Equity Incentive Plan, as amended

10-K

000-33043 10.14

3/23/2007

10.10*

2009 Equity Incentive Plan, as amended

10-Q

000-33043

10.2

8/9/2013

10.11*

10.12*

10.13*

Form of Option Grant Notice and Form of Option Agreement
for 2009 Equity Incentive Plan, as amended

Form of Restricted Stock Unit Grant Notice and Form of
Restricted Stock Unit Award Agreement for 2009 Equity
Incentive Plan, as amended

Form of Restricted Stock Bonus Grant Notice and Form of
Restricted Stock Bonus Agreement for 2009 Equity Incentive
Plan, as amended

10-K

000-33043 10.16

3/11/2011

10-K

000-33043 10.17

3/11/2011

10-K

000-33043 10.18

3/11/2011

10.14*

Form of Change of Control Agreement

10-K

000-33043 10.26

3/16/2006

10.15*

Addendum to Form of Change of Control Agreement dated
December 30, 2010

10-K

000-33043 10.24

3/11/2011

10.16*

2010 Omnicell Quarterly Executive Bonus Plan

8-K

000-33043

10.1

3/17/2010

Table of Contents

Exhibit
Number
10.17*

10.18*

10.19*

10.20*

10.21*

10.22*

10.23*

10.24*

10.25*

Exhibit Description

Form

File No.

Exhibit

Filing Date

Incorporated By Reference

Employment Agreement, dated October 31, 2003, between
Omnicell and Dan S. Johnston

Addendum to Offer Letter, dated December 30, 2010, between
Omnicell and Dan S. Johnston

Employment Agreement, dated November 28, 2005, between
Omnicell and Robin G. Seim

Addendum to Offer Letter, dated December 30, 2010, between
Omnicell and Robin G. Seim

Addendum to Change in Control Severance Letter between
Omnicell and Robin G. Seim dated December 30, 2010

Employment Agreement, dated October 17, 2008, between
Omnicell and Nhat H. Ngo

Addendum to Change in Control Severance Letter between
Omnicell and Nhat H. Ngo dated December 30, 2010

Employment Agreement, dated December 5, 2008, between
Omnicell and Marga Ortigas-Wedekind

Addendum to Change in Control Severance Letter between
Omnicell and Marga Ortigas-Wedekind dated December 30,
2010

10-K

000-33043 10.26

3/8/2004

10-K

000-33043 10.14

3/11/2011

8-K

000-33043

10.1

1/24/2006

10-K

000-33043 10.21

3/11/2011

10-K

000-33043 10.22

3/11/2011

10-K

000-33043 10.29

2/24/2009

10-K

000-33043 10.28

3/11/2011

10-K

000-33043 10.31

2/24/2009

10-K

000-33043 10.30

3/11/2011

10.26

Lease between Omnicell, Inc. and Sycamore Drive Holdings,
LLC, dated March 16, 2012

8-K

000-33043

10.1

3/20/2012

10.27* +

10.28*

10.29*

10.30

10.31

10.32

10.33

10.34

10.35

10.36+

Omnicell, Inc. Amended and Restated Severance Benefit Plan

Form of Restricted Stock Unit Award Agreement for the 2009
Equity Incentive Plan, as amended

Form of Performance Cash Award Grant Notice and Form of
Performance Cash Award Agreement for the 2009 Equity
Incentive Plan, as amended

Lease, between Medical Technologies Systems, Inc. and
Gateway Business Centre, Ltd., dated March 31, 2004

First Lease Amendment, between Medical Technologies
Systems, Inc. and Gateway Business Centre, Ltd., dated July
26, 2004

Lease, between MTS Medication Technologies, Ltd. and SAL
Pension Fund, Ltd., dated June 9, 2011

Third Amendment to Lease, between PR Amhurst Lake LLC
and Omnicell, Inc., dated July 1, 2013

Credit Agreement between Omnicell, Inc., and lenders, dated
September 25, 2013

Amendment Number One to Credit Agreement, dated
November 5, 2014, by and among Omnicell, Inc., with respect
to Section 12 thereof, the Subsidiary Guarantors and Wells
Fargo Bank, National Association, as administrative agent
Second Amendment to Office Lease, dated December 17,
2014, by and between Omnicell, Inc. and Point Place, LLC

10-Q

000-33043

10.4

8/9/2012

10-Q

000-33043

10.5

8/9/2012

10-Q

000-33043

10.6

8/9/2012

10-Q

000-33043

10.7

8/9/2012

10-Q

000-33043

10.8

8/9/2012

10-Q

000-33043

10.1

8/9/2013

8-K

000-33043

10.1

9/26/2013

8-K

000-33043

10.1

11/7/2014

Table of Contents

Exhibit
Number
10.37+

21.1+

23.1+

23.2+

24.1+

31.1+

31.2+

32.1+

101.INS+

Exhibit Description

Form

File No.

Exhibit

Filing Date

Incorporated By Reference

Agreement for Lease relating to Two Omega Drive, River
Bend Technology Centre, Iram, dated January 14, 2015,
between Omega Technologies Limited and MTS Medication
Technologies Limited and Omnicell, Inc.
Subsidiaries of the Registrant

Consent of Independent Registered Public Accounting Firm

Power of Attorney (included on the signature pages hereto)

Certification of Chief Executive Officer, as required by Rule
13a-14(a) or Rule 15d-14(a)

Certification of Chief Financial Officer, as required by Rule
13a-14(a) or Rule 15d-14(a)

Certification of Chief Executive Officer and Chief Financial
Officer, as required by Rule 13a-14(b) or Rule 15d-14(b) and
Section 1350 of Chapter 63 of Title 18 of the United States
Code (18 U.S.C. §1350) (1)
XBRL Instance Document (2)

101.SCH+

XBRL Taxonomy Extension Schema Document (2)

101.CAL+ XBRL Taxonomy Extension Calculation Linkbase Document

101.DEF+

(2)
XBRL Taxonomy Extension Definition Linkbase Document (2)

101.LAB+ XBRL Taxonomy Extension Labels Linkbase Document (2)

101.PRE+

XBRL Taxonomy Extension Presentation Linkbase Document
(2)

_________________________________________________

(1)

(2)

Indicates a management contract, compensation plan or arrangement.

Filed herewith.

This certification accompanies the Form 10-K to which it relates, is not deemed filed with the Securities and Exchange
Commission and is not to be incorporated by reference into any filing of the Registrant under the Securities Act of
1933, as amended, or the Securities Exchange Act of 1934, as amended (whether made before or after the date of the
Form 10-K), irrespective of any general incorporation language contained in such filing.

Pursuant to applicable securities laws and regulations, the Registrant is deemed to have complied with the reporting
obligation relating to the submission of interactive data files in such exhibits and is not subject to liability under any
anti-fraud provisions of the federal securities laws as long as the Registrant has made a good faith attempt to comply
with the submission requirements and promptly amends the interactive data files after becoming aware that the
interactive data files fail to comply with the submission requirements. These interactive data files are deemed not filed
or part of a registration statement or prospectus for purposes of sections 11 or 12 of the Securities Act of 1933, as
amended, are deemed not filed for purposes of section 18 of the Securities Exchange Act of 1934, as amended, and
otherwise are not subject to liability under these sections.