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Cerner

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FY2014 Annual Report · Cerner
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World Headquarters

Cerner Corporation

2800 Rockcreek Parkway

Kansas City, MO USA 64117

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Worldwide

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Health care is too important to stay the same.TM

cerner.com

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Cerner Corporation      2014 Annual Report

4/6/15  8:45 AM

Cerner connects people and systems through our open, powerful and versatile platforms 
and solutions, providing information where it’s needed most. Together with 
our clients and industry collaborators, we’re creating a future where the health system 
works to improve the well-being of individual people and entire populations.

© Cerner Corporation. All Rights Reserved. All Cerner trademarks and logos are owned or licensed by Cerner Corporation

and/or its affiliates. All other brand or product names are trademarks or registered marks of their respective owners.

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4/6/15  8:45 AM

Cerner Corporation 
2014 Annual Report

Table of Contents: Annual Report 2014

Board of Directors  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  2 
Leadership  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 3
Cerner’s Long-Term Performance  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 4
Letter to Our Shareholders, Clients and Associates   .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 5
Appendix: Reconciliation of 2014 Non-GAAP Results to GAAP Results .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  16
Form 10-K  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  18
Business and Industry Overview .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  20
Risk Factors .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  27
Properties  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .37

  Market for the Registrant’s Common Equity, Related Stockholder Matters 

and Issuer Purchases of Equity Securities  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  38
Selected Financial Data   .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 39
  Management’s Discussion and Analysis of Financial Condition and Results of Operations  .  .  .  .  .  .  .  . 40
  Quantitative and Qualitative Disclosures About Market Risk .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .53
Controls and Procedures  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .53
Security Ownership of Certain Beneficial Owners and Management and 
Related Stockholder Matters .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 56
Exhibits and Financial Statement Schedules  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .57
Reports of Independent Registered Public Accounting Firm  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 62
Consolidated Balance Sheets  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 64
Consolidated Statements of Operations  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 65
Consolidated Statements of Comprehensive Income   .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 66
Consolidated Statements of Cash Flows .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .67
Consolidated Statements of Changes in Shareholders’ Equity  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 68
Notes to Consolidated Financial Statements  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 69
Basis of Presentation, Nature of Operations and Summary of Significant Accounting Policies   .  .  . 69
Business Acquisitions  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .73
Investments  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  76
Fair Value Measurements .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  77
Receivables  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  78
Property and Equipment  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  79
  Goodwill and Other Intangible Assets  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  79
Software Development  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 80
Long-term Debt and Capital Lease Obligations  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 80
  Hedging Activities   .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 81
Contingencies  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  82
  Other Income  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  83
Income Taxes  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  83
Earnings Per Share  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 85
Share-Based Compensation and Equity  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 86
Foundations Retirement Plan  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 88
Related Party Transactions .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 89
Commitments   .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 90
Segment Reporting  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 91
  Quarterly Results .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 92
Stock Price Performance Graph  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  93
Corporate Information   .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  .  . 94

1

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Board of Directors

Neal L. Patterson 

Chairman of the Board, Chief Executive Officer,  
and Co-founder, Cerner Corporation

Clifford W. Illig 

Vice Chairman and Co-founder, Cerner Corporation

Gerald E. Bisbee Jr., Ph.D. 

Chairman, Chief Executive Officer, and Co-founder,  
The Health Management Academy

Former Chairman, Chief Executive Officer and President,  
ReGen Biologics, Inc., 1998–September 2011

Denis A. Cortese, M.D. 

Emeritus President and Chief Executive Officer, Mayo Clinic

Foundation Professor, Arizona State University School  
of Health Management and Policy

Director of Arizona State University’s Health Care  
Delivery & Policy Program

President of the Healthcare Transformation Institute  

The Honorable John C. Danforth  Retired Partner, Bryan Cave LLP, January 1995–September 2014

Ambassador to the United Nations, July 2004–January 2005

U.S. Senator, Missouri, 1976–1995

Mitchell E. Daniels, Jr. 

President, Purdue University

Governor of the State of Indiana, January 2005–January 2013

Linda M. Dillman 

Chief Information Officer, QVC, Inc.

Senior Vice President of Enterprise Services/Global Functions IT,  
Hewlett-Packard Company, August 2009–January 2012

Executive Vice President of Benefits and Risk Management,  
Wal-Mart Stores, Inc., April 2006–July 2009

Executive Vice President and Chief Information Officer,  
Wal-Mart Stores, Inc., August 2002–April 2006

William B. Neaves, Ph.D. 

President Emeritus and Director, The Stowers Institute for   
Medical Research

William D. Zollars 

Former Chairman, Chief Executive Officer and President,    
YRC Worldwide, November 1999–July 2011

2

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Leadership

Cerner Executive Cabinet 

Neal L. Patterson • Chairman of the Board, Chief Executive Officer and Co-founder
Clifford W. Illig • Vice Chairman and Co-founder
Zane M. Burke • President
Marc G. Naughton • Executive Vice President and Chief Financial Officer
Michael R. Nill • Executive Vice President and Chief Operating Officer
Jeffrey A. Townsend • Executive Vice President and Chief of Staff
Julia M. Wilson • Executive Vice President and Chief People Officer
Joanne M. Burns • Senior Vice President and Chief Strategy Officer 
John P. Glaser • Senior Vice President, Health Policy
Michael C. Neal • Senior Vice President, Professional Services
John T. Peterzalek • Senior Vice President, Client Relationships
Matthew J. Swindells • Senior Vice President, Population Health
Donald D. Trigg • Senior Vice President and President, Cerner Health Ventures

Cerner Executive Management  Don D. Bisbee • Senior Vice President, Strategic Business Units

Client Organization 

Kathleen M. Chaffee • Senior Vice President, Population Health Advisory Services 
L. Mitchell Clark • Senior Vice President and General Manager, CommunityWorks 
Stephen W. Eckman • Senior Vice President, Application Services 
Ed L. Enyeart • Senior Vice President, Finance
Richard J. Flanigan • Senior Vice President and President, Cerner Health Services
William E. Graff • Senior Vice President, Cerner Technology Services 
Ryan R. Hamilton • Senior Vice President, Population Health Intellectual Property Development
Richard W. Heise • Senior Vice President, Revenue Cycle 
Eva L. Karp • Senior Vice President, Chief Clinical Operations Officer and  

    General Manager, Clinical ABUs 

David P. McCallie, Jr., M.D. • Senior Vice President, Medical Informatics 
Douglas S. McNair, M.D. & Ph.D. • Senior Vice President, Cerner Corporation and  

          President, Cerner Math 

Rama Nadimpalli • Senior Vice President and General Manager, Cerner India 
Max A. Reinig • Senior Vice President, Intellectual Property Development 
Farrell L. Sanders • Senior Vice President and Chief Operating Officer, Cerner Health Services
Kent C. Scheuler • Senior Vice President, CernerWorks
Randy D. Sims • Senior Vice President, Chief Legal Officer and Secretary
Shellee K. Spring • Senior Vice President, Ambulatory and Client Experience
Michael R. Battaglioli • Vice President and Chief Accounting Officer 
Gay M. Johannes • Vice President and Chief Quality Officer 
Allan O. Kells • Vice President, Investor Relations

G. Ben Hilmes • Senior Vice President, US East 
E. Tim Kostner • Senior Vice President, Client Development  
Jay E. Linney • Senior Vice President, US West 
Sam P. Pettijohn • Senior Vice President and General Manager, Investor Owned  
Robert J. Shave • Senior Vice President, Cerner Corporation and President, Cerner Canada 
Cameron D. Burt • Vice President and General Manager, Australia 
Michael J. McHugh • Vice President, Cerner Health Services 
Emil E. Peters • Vice President and Managing Director, Europe  
Michael A. Pomerance • Vice President and General Manager, Middle East
Geoff Segal • Vice President and General Manager, United Kingdom and Ireland
Arne Westphal • Vice President and General Manager, Germany
Israel D. Armstrong • General Manager, Brazil 
Holger Cordes • Chief Operating Officer, Europe 
David E. Corcos • Regional General Manager, Belgium, France, Netherlands,  

             Sweden and Switzerland

Amanda J. Green • Regional General Manager, Denmark, Ireland and Norway 
Rebecca A. LaNasa • Regional General Manager, Southeast Asia
Jose Maniega • Regional General Manager, Portugal and Spain 
Stefan Radatz • General Manager, Austria

3

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Cerner’s Long-Term Performance

The following table provides a view of our growth over the last decade and since we first became a 
publicly traded company in 1986.

i

e
n
L
p
o
T

Bookings

Revenue

Domestic Revenue 

Global Revenue 

Revenue Backlog

i

Adjusted Operating Margin1

e Adjusted Operating Earnings1
n
L
m
o
t
t
o
B

Adjusted Net Earnings1

Adjusted Diluted Earnings Per Share1

t Total Assets
e
e
h
S
e
c
n
a
l
a
B

Total Debt

Cash and Investments

Days Sales Outstanding

Equity

w Operating Cash Flow
o
F

Free Cash Flow1

l

t

h Capital Expenditures
w
o
r
G
n

R&D Spending

Associate Headcount

i

Market Capitalization

e Cerner Stock Price
c
n
a
m
r
o
f
r
e
P

S&P 500 Index

NASDAQ Composite Index

h
s
a
C

t
n
e
m
t
s
e
v
n
I

t
e
k
r
a
M

1986

2004

2014

2004–2014

1986–2014

Compound Annual Growth Rates

Previous Decade

Since Going Public

$18

$17

$17

 $917

 $4,250 

 $926 

 $3,403 

 $862 

 $3,022

$0.2

 $64 

 $381 

$11

$3

 $1,539

 $10,617 

 $115 

 $842

14.8%

12.4%

24.7%

$2

 $65 

 $576 

$0.01

 $0.22 

 $1.65 

$26

$8

161

$1

$16

$1

-$1

$1

$2

 $982

 $4,531 

 $190 

 $1,652

 104 

 $131

 66 

 $130

 $597

 $3,566 

 $168

 $847 

 $53 

 $393 

 $56 

 $277 

 $188 

 $467 

 149 

 5,345 

 15,800 

$0.24

 $6.65

 $64.66

$45

349

242

 $1,948

 $22,135

 2,175

 1,212

 4,736 

2,059

17%

14%

13%

20%

21%

22%

24%

23%

17%

24%

-4%

0%

20%

18%

22%

17%

10%

11%

26%

28%

8%

5%

22%

21%

20%

31%

28%

22%

22%

20%

20%

21%

-3%

19%

21%

27%

NM

22%

22%

18%

22%

25%

10%

8%

NOTES
Dollars are in millions except Adjusted Diluted Earnings Per Share and stock prices.
Free Cash Flow represents cash flows from operating activities less capital purchases and capitalized software development costs. 
NM = Not Meaningful

1  Adjusted operating earnings, adjusted operating margin, adjusted net earnings, adjusted diluted earnings per share, and free cash flow reflect 
adjustments compared to results reported on a Generally Accepted Accounting Principles (GAAP) basis. Non-GAAP results should not be 
substituted as a measure of our performance but instead should be used along with GAAP results as a supplemental measure of financial 
performance. Non-GAAP results are used by management along with GAAP results to analyze our business, to make strategic decisions, to 
assess long-term trends on a comparable basis, and for management compensation purposes. Please see the appendix following the Letter  
to Our Shareholders, Clients and Associates for a reconciliation of these items to GAAP results.

4

 
 
 
 
 
 
A Letter to Our Shareholders, Clients and Associates

In 2014, Cerner had another strong year financially, 
operationally  and 
strategically,  which  also 
translated  into  a  good  year  for  our  shareholders. 
We  continued  to  position  our  company  for  long-
term  success  through  significant  investments  in 
research and development focused on population 
health,  physician  experience,  open  platforms, 
revenue cycle and mobility. We also announced the 
acquisition of Siemens Health Services. I will share 
more  details  later  in  the  letter,  but  first,  I’d  like  to 
provide some highlights of our financial results. 

•  We had record bookings of $4.25 billion, 

reflecting 13% growth over 2013.  

•  Our revenue backlog grew 19% and eclipsed 

$10.6 billion, providing a high level of visibility 
into future revenue.

•  Total revenue grew 17% to a record $3.4 

billion. Below is a breakdown of revenue by 
business model for the year: 

o  Licensed Software grew 17% to 

$453 million; 

o  Technology Resale grew 4% to  

$273 million; 

o  Subscriptions and Transactions increased 

12% to $220 million; 

o  Professional Services revenue grew  

28% to $1.09 billion; 

o  Managed Services increased 15% to  

$549 million; 

o  Support & Maintenance was up 9% to  

$725 million; and 

o  Reimbursed Travel was $90 million,  

which is up 28%.

•  Our adjusted operating earnings1 grew 15% 
and our adjusted EPS1 of $1.65 reflects 
growth of 17%. 

•  Our adjusted operating margin1 of 24.7% 
reflects a slight drop from 25.1% in 2013, 
mainly due to a mix of revenue that had 
higher third-party costs in 2014 compared 
to 2013.

•  We ended 2014 with a strong cash and 

investment balance of $1.65 billion, which is 
up over $200 million from 2013 even after 
investing over $465 million in R&D and $275 
million in capital expenditures to support 
our growth. This strong cash and investment 
position funded our $1.37 billion acquisition 
of Siemens Health Services, which closed on 
February 2nd of this year.

Apart  from  the  financial  growth,  we  grew 
throughout  2014  in  other  meaningful  ways—
clients,  countries,  patents  and  associates.  We 
ended the year with nearly 16,000 associates, and 
that  was  before  we  added  our  Siemens  Health 
Services associates in February 2015.

Cerner’s  success  puts  us  on  the  radar  to  get 
recognized by business analysts and publications 
on  annual  lists  that  use  superlatives  like  “best,” 
“most  competitive,”  “elite”  and  “top.”  It’s  fun, 
and  it’s  the  kind  of  stuff  that  makes  parents 
beam.  My  personal  philosophy  (and  advice  to 
any Cerner associates reading) is to focus less on 
reading  the  press  and  more  on  being  worthy  of 
what has been said about us. As we begin 2015, 
we  are  simultaneously  recognized  by  Forbes  as 
one of the “World’s Most Innovative Companies” 
and  by  Fortune  as  one  of  the  “World’s  Most 
Admired Companies.” We’re honored, but we also 
recognize that those are tall orders to fill.  Every 
day we see things that can and must be better.

Frankly,  one  of  the  best  things  about  a  pattern 
of  success  is  that  it  reinforces  our  resolve  to 
pursue  long  term  objectives,  knowing  today’s 
long-term is tomorrow’s present. When you lead 
through vision, confidence that the future will be 
greatly  different  from  the  present  is  essential. 
Communication is also essential. In order to read a 
map, you need to know two pieces of information: 
where you are and where you’re going. At least a 
few times a year, I use internal notes to all Cerner 
associates  to  communicate  important  things 
about  both  our  current  coordinates  and  our 
destination. And, although there is a very public 
audience for this note, I try to do the same thing 
here. There are always more potential topics than 

5

time to write about them. For this letter, I’ve tried 
to choose some topics that will give you a sense 
of our year, our environment at the intersection of 
health care and IT, and where our journey might 
take us next.

THE RIGHT TIME AND PLACE FOR A BOLD MOVE: 
THE SIEMENS HEALTH SERVICES ACQUISITION

To understand the respect I have for the core of 
Siemens Health Services, you would have to travel 
back  in  time  to  1979  when  Cerner  was  founded. 
Shared  Medical  Systems  (or  SMS)  was  the 
dominant company then, a pioneer and innovator 
in  health  IT.  In  some  ways,  it  was  the  strength 
of  SMS  in  patient  billing  and  revenue  cycle 
management in the 1970s and 1980s that shaped 
Cerner’s  choice  to  become  a  “clinical  systems” 
company.  German  multinational  conglomerate 
Siemens AG bought the company in 2000, seeing 
the  strategic  nature  of  IT  in  shaping  health  care 
delivery.  Siemens  was  right  about  the  strategy, 
but  I  believe  the  pace  of  change  of  health  IT, 
which has been accelerated by Meaningful Use in 
the U.S., made Siemens Health Services more of a 
distraction to the parent company than an asset. 
Health IT is our sole focus. We saw an opportunity, 
and we liked it.

I have said and still maintain that I don’t believe 
you  can  build  a  company  through  acquisitions. 
The core must be based on your commitment to 
your vision, and it grows organically. For 35 years, 
we  have  built  Cerner  organically  by  investing  in 
the development of our own intellectual property, 
much  of  it  software  but  also  valuable  content, 

algorithms, models and data built for a common 
architecture  and  its  platforms.  The  belief  that 
Architecture  Matters  has  served  Cerner  well, 
and  integration  is  a  strategy  that  has  been 
validated resoundingly in the marketplace. As we 
have  grown,  we’ve  strategically  acquired  a  few 
wonderful smaller companies along the way with 
good  technology  and  talent,  but  the  acquisition 
of  a  billion-dollar  business  unit  with  multiple 
distinct  platforms  and  architectures  was  not  a 
natural thing for us.

We didn’t need to make the acquisition, but the 
reasons for wanting to were clear to us. It would 
expand the base into which we can sell our broad 
range of solutions and services. It would augment 
our non-U.S. growth opportunities through a large 
global  presence.  It  would  increase  our  ability  to 
continue  investing  heavily  in  R&D.  And  it  would 
add  thousands  of  highly  skilled  associates  that 
could enhance Cerner’s capabilities. 

We  have  been  clear  with  the  Health  Services 
clients that we will support the Soarian platform 
for  a  very  long  time.  All  of  the  platforms  we 
investment 
acquired  will  need  support  and 
sufficient  to  validate  the  investment  and  the 
choice  the  clients  have  made  in  selecting  them. 
We understand their needs well, because they’re 
the  same  as  the  rest  of  our  clients.  Having  said 
that,  Millennium  and  HealtheIntent  are  our  EMR 
and population health platforms. They’re proven, 
powerful,  flexible  and  scalable,  and  they  will  be 
our clients’ paths to the future. Siemens is a major 
health care company outside of health IT, and it 
cared deeply that its clients were in the hands of 

1979

1982

1984

1986

Neal Patterson, Paul Gorup, and 
Cliff Illig leave Arthur Andersen & 
Co. to form their own company

PathNet® is installed in the lab  
at St. John Medical Center in 
Tulsa, Oklahoma

Cerner secures $1.5 million 
venture capital funding 
from First Chicago  
Capital Corporation

Cerner goes public and is  
listed on NASDAQ (CERN)

$17 million of revenue

149 associates

1987

Cerner listed as one 
of Inc. magazine’s 
100 fastest-growing 
companies

6

an  organization  that  could  address  their  health 
IT needs in the future. Cerner’s platforms are the 
path to the future, but it will not be a journey of 
one  year  or  even  five  in  many  cases.  We  will  all 
arrive at the same destination.

The battle for talent is one of our toughest fronts. 
From  January  2012  to  January  2015,  before  the 
acquisition,  Cerner  hired  more  than  5,500  net 
new associates, with plans to add even more. The 
acquisition  brought  more  than  5,000  associates 
with a great deal of specific health IT knowledge 
that  is  complementary  to  our  own.  I  visited  the 
Malvern,  PA,  headquarters  of  Health  Services 
shortly  after  the  acquisition  closed,  and  I  held 
back-to-back town halls with as many associates 
as  we  could  fit  in  the  auditorium  there.  I  was 
very  impressed  with  the  associates  I  met.  Their 
strength  in  billing  and  revenue  cycle  goes  back 
decades,  and  there  is  also  some  wonderful 
expertise  in  workflows  and  a  large  global  base 
of  associates.  We  were  in  the  same  industry 
following  paths  that  led  to  different  outcomes, 
with different strengths. We have a great deal to 
learn from each other. I am convinced we will be 
stronger together. Together we will be focused on 
using IT as the lever to help our clients produce 
the best possible health outcomes at the lowest 
attainable cost.

Remarkably, combining our organizations allows 
us to not only combine talent, but also to invest 
an expected $650 million a year in research and 
development  for  the  rest  of  the  decade.  We 
believe there is no company that will match this 
level of investment in health IT. It’s a good thing....
we are going to need a lot of strength in the next era. 

In short, the combination of Health Services with 
Cerner  makes  us  a  stronger  company,  with  new 
opportunities  to  make  it  even  better.  Only  time 
will  tell  how  successful  we  are,  but  it  is  already 
clear  that  it  is  a  wonderful  set  of  new  clients  
and associates.

OUR SIZE AND SKILLS

Health  care  is  huge,  and  it’s  worldwide.  We 
believe that size, scale and skills are important to 
partner with health care providers to solve their 
challenges  today  and  prepare  for  an  uncertain 
future.  An  anecdote  about  size:  In  October,  we 
made  a  difficult  decision  to  cancel  our  planned 
companywide  Town  Hall,  in  part  because  it 
would  have  caused  a  traffic  jam  in  downtown 
Kansas  City.  Associates  still  wanted  to  meet,  so 
I chose to make a whistle-stop tour of a number 
of  our  campuses.  Those  meetings  with  groups 
of  200  to  500  associates  turned  out  to  be  one 
of the highlights of my year. Growth can have its 
challenges,  but  it’s  also  exciting  to  expand  the 
boundaries and see what we can create together. 

As  I  write  this  memo  in  March  2015,  we  are  at 
a  size  that  we  probably  didn’t  imagine  even 
10  years  ago.  Cerner  is  on  a  very  short  list  of 
companies that have consistently performed well 
throughout  a  decades-long  winnowing  of  the 
health  IT  industry.  Today,  we  are  a  roughly  $25 
billion  market  cap,  highly  profitable  company 
with  a  strong  balance  sheet,  growing  at  double 
digit  rates  in  all  categories.  We  have  more  than 
20,000  associates  and  a  presence  in  more  than 
30 countries. We have a singular focus on health 

1990

1992

1993

1994

Revenues surpass $50 million

2 for 1 stock split (May 12)

2 for 1 stock split (March 1)

1,000 associates

Cerner Vision Center opens

Revenues surpass  
$100 million

1995

2 for 1 stock split 
(August 7)

7

IT. We’re halfway through the biggest decade of 
change in health care to date—and we have seen a 
lot of big, change-filled decades. Every U.S. client 
we have is concerned about cost and quality, ICD-
10,  Meaningful  Use  Stage  3,  and  the  transition 
away from fee-for-service reimbursement. Every 
client outside the U.S. has a similar list of critical 
environmental 
issues  creating  the  need  for 
fundamental change. The list of challenging work 
ahead is huge, but nearly all of it is resourced, with 
good  talent  driving  us  forward.  We  have  a  very 
good opportunity to finish the decade strong and 
make a real impact on health and care.

Size  matters  because  health  care  is  the  largest 
sector in almost all worldwide economies. It has 
tremendous complexities, breadth and reach. Our 
size alone is of no value without vision, agility and 
real skills.  

In  the  next  section,  I  want  to  talk  about  a  client 
engagement that is making use of vision, agility 
and  skills  to  advance  clinical  computing  beyond 
its  current  state,  creating  the  v2.0  EHR  and 
Revenue Cycle instance for the industry. 

THE INTERMOUNTAIN MODEL

In  last  year’s  letter,  we  had  already  signed 
our  multi-year  strategic  partnership  with 
Intermountain  Healthcare,  but  I  chose  not  to 
write about it because it was not “live” yet. Now 
that  we’re  beginning  to  bring  sites  live  there,  I 
want to share more about this very special client 
relationship and engagement. 

Intermountain 
iconic  health  system 
with  22  hospitals  and  more  than  180  clinics 

is  an 

in  Utah.  They  are  widely  viewed  as  a  model 
health  system  because  of  their  track  record 
of  providing  high  quality  care  at  low  cost—the 
holy  grail  of  health  care.  Somewhat  amusingly, 
in  2012,  Intermountain’s  excellence  was  one  of 
the  few  points  mutually  agreed  upon  by  both 
Democratic  and  Republican  candidates  Barack 
Obama and Mitt Romney in the first presidential 
debate.  Intermountain  also  has  a  special  claim 
to  fame  as  the  home  of  Dr.  Homer  Warner,  one 
of  the  undisputed  fathers  of  clinical  computing.  
Dr.  Warner  was  a  cardiologist  who  saw  the 
enormous potential impact that computing would 
have on the practice of medicine and acted on it, 
helping to pioneer the field of medical informatics. 
Because of Homer Warner’s legacy, Intermountain 
has been using computers in medicine since the 
1950s. That is not a typo. In the 1980s, I used to 
go to Salt Lake City to listen to Dr. Warner speak, 
soaking up some of the insights that would pour 
out of his prodigiously creative mind and soul. 

Needless  to  say,  when  we  learned  in  2012  that 
Intermountain was looking for a commercial EHR 
to  continue  its  work,  our  interest  was  beyond 
piqued.  Throughout  2013,  we  participated  in 
a  highly  competitive,  head-to-head  selection 
process.  In  the  end,  we  were  chosen.  The 
Intermountain  executive  team  voiced  several 
reasons—a mix of system capabilities in the present 
with  adaptability  for  the  future,  a  commitment 
to  support  new  payment  models  and  the  open 
interchange  of  information,  and  the  ability  to 
support the continuation of their very important 
innovations around quality, safety and cost. And 
significantly,  they  also  spoke  of  something  else 

1999

2000

2001

2002

2003

HNA Millennium® Phase 1 is completed

3,000 associates

Revenues surpass $500 million

4,000 associates

Cerner makes Fortune list of  
“Best 100 Companies to Work For”

Cerner and Atos Origin 
awarded UK National  
Health Services Choose  
and Book contract

8

we felt from the earliest meetings—an alignment 
of cultures and a shared vision for the future. 

The full project commenced with contract signing 
in  late  November  2013.  It  was  slated  to  replace 
their  current  ambulatory,  inpatient  and  revenue 
cycle  systems  across  all  facilities.  They  call  the 
project iCentra, a combination of some letters in 
the names Intermountain and Cerner.  Embedded 
in  the  iCentra  project  and  platform  are  several 
triggers  for  helping  support 
Intermountain’s 
stated goal of “helping people live the healthiest 
lives  possible.”  We  converted  the  first  phase  of 
the  project  in  early  2015  with  two  hospitals  and 
20  clinics  coming  live  in  February,  15  months 
after contract signing. In an industry where large 
health system conversions can take years, this is 
a  significant  accomplishment.  We  will  continue 
bringing  hospitals  and  clinics  online  throughout 
the  remainder  of  2015  and  into  2016.  The  real 
focus,  however,  is  less  on  dates  on  a  calendar 
and more on creating a flexible and long-lasting 
platform to innovate, learn and improve.    

When  a  health  system  adopts  a  completely 
integrated system, the act of conversion changes 
the  workflow  of  every  doctor,  every  nurse  and 
almost every dollar of revenue. It also completely 
alters  the  existing  ecosystem  of  information 
technologies that have been in place for decades. 
I  have  always  called  health  IT  conversions  the 
organizational  equivalent  of  organ  transplant 
surgery.  We  are  just  a  month  or  so  out  of  the 
operating  room  at  this  point,  but  I  can  report 
that the patient is doing well. Within a couple of 
months post conversion, the shock to the system 

usually wears off and the users gain a new level 
of familiarity and trust in the new systems. With 
20 hospitals left to come online, we expect some 
bumps  in  the  road  ahead,  but  we  are  also  very 
excited.  Overall,  it  has  been  an  extraordinary 
project that has now had an auspicious launch.

This is the first Cerner project to make use of our 
new  Agile  Deployment  Methodology,  a  model 
that  represents  a  departure  from  the  industry-
standard  waterfall 
implementation  process. 
In  the  Agile  model,  physicians  and  other  end 
users participate in the system build and design, 
and  never  go  more  than  six  weeks  without  the 
opportunity to see, use and give feedback on the 
system  prior  to  go-live.  We  don’t  want  to  give 
away  all  of  our  secrets,  but  it’s  a  great  process 
with  benefits  that  will  extend  beyond  go-live  as 
well. We believe it might even be the keystone that 
supports the other elements of a learning health 
system, another of medicine’s elusive grails. 

Intermountain  made  it  clear  from  the  start  that 
they  were  enthusiastic  about  being  an  “all-in” 
proof  point  for  Cerner’s  capabilities.  They  were 
also  excited  about  the  potential  for  the  iCentra 
work  to  positively  impact  other  health  systems. 
Using capabilities that already exist in Millennium 
and some that have been developed together, our 
combined teams have built out hundreds of health 
care  roles  and  hundreds  of  clinical  workflows 
across 50+ medical specialties and subspecialties. 
There  are  also  350+  financial  workflows,  with 
detailed  workflows  defined  that  are  multi-role, 
multi-venue. In some cases, we’re getting down to 
the condition level. Together we’re fully leveraging 

2004

2005

2006

2007

Cerner celebrates 25th anniversary

Revenues surpass $1 billion

2 for 1 stock split (Jan. 10)

Revenues surpass $1.5 billion

Cerner ranks third among software 
companies in The Wall Street Journal’s  
Top 50 Returns over a five-year period

5,000 associates

Nearly 7,000 associates

Introduced CareAware® device 
architecture and line of devices

Cerner signs contract with BT for 
London region of NHS program

First Cerner Millennium® site  
in France

Opened Cerner Healthe Clinic  
at World Headquarters

Shipped first production units of  
RxStation® medication dispensing  
devices; 25 clients purchase  
CareAware iBus® device connectivity

Delivered new Cerner ProVision®  
PACS Workstation

Opened new Data Center at  
World Headquarters

Signed first clients in Spain and Egypt;  
opened office in Dublin, Ireland

Acquired Etreby Computer Company  
(retail pharmacy solutions)

9

iCentra  capabilities  like  MPages,  Discern  Rules 
and  order  sets  to  embed  the  evidence-based 
models  of  care  that  Intermountain  is  known  for. 
For  years  Intermountain’s  Care  Process  Models 
and  Clinical  Process  Guidelines  have  helped 
its  clinicians  achieve  high  quality  care  and  low 
overall  cost.  Now  they’re  moving  from  paper 
documents  into  digital  workflows  that  are  used 
every  day.  In  Intermountain  quality  guru  Brent 
James’  terms,  the  goal  is  to  provide  “the  best 
patient care currently available, at an executable 
level where we consistently perform on behalf of 
our  patients.”  In  Cerner’s  terms,  it’s  to  eliminate 
all  avoidable  error,  variance,  waste,  delay  and 
friction from health care.

This  project  has  great  visibility.  As  it  continues 
to roll out, we believe it will become our version 
2.0  Millennium  to  meet  the  complex  needs  of 
providers  across  the  spectrum  of  health  care, 
coordinating  care  any  time,  any  place,  using 
intelligence  to  inform  decisions  by  the  highest 
standards,  connecting  all  of  the  individuals  they 
serve  seamlessly  into  the  process.  It’s  exciting 
stuff.  There  is  far  too  much  to  explain  here,  but 
hopefully I have given you a sense of why we are 
so enthusiastic about it. 

INTEROP: AN INSIDE STORY

There  is  a  story  within  a  story  playing  out  in 
the  health  IT  industry  around  how  our  health 
information  should  be  shareable  and  accessible 
among  our  primary  care  physicians,  specialists, 
hospital physicians and selves. In the past couple 
of  years,  the  public  discourse  around  the  lack 

of  interoperability  among  health  IT  systems 
has  at  times  reached  an  almost  fevered  pitch, 
partly because of competitive marketplaces, but 
principally  because  the  decisions  around  the 
availability and safe handling of health information 
are very sensitive and have real consequences in 
terms  of  how  care  is  provided  when  we  or  our 
loved ones are sick. In recent years, a great deal 
of money has been spent on health IT—over $27 
billion directly from the U.S. federal government 
to  eligible  providers  and  hospitals  for  the 
purpose of creating a digital health care system. 
And while that has largely occurred, the day-to-
day  lack  of  interoperability  across  health  care 
organizations and platforms limits the benefits to 
us  as  individuals  and  creates  huge  costs  to  the 
entire  system.  Interoperability  in  health  IT  is  not 
entirely comparable to the interoperability found 
among personal computing platforms, telephony 
components,  music  services  or  even  banking 
systems,  although  it  has  some  similarities.  The 
key  differences  are  a  result  of  the  degree  of 
complexity, privacy, importance and data diffusion 
found  in  health  care.  Health  information  is  very 
complex—as  complex  as  systems  of  the  body, 
the  wide  world  of  diseases,  and  the  burgeoning 
sciences. It’s also highly private—dealing with the 
most  intimate  details  of  our  bodies  and  lives.  It 
is  critically  important—in  the  moment  you  need 
it, it can have life or death importance. And it is 
highly diffused—in the United States, the average 
person  has  seen  18  different  doctors,  a  number 
that  increases  to  28  doctors  if  you’re  over  652. 
Each of your physicians has pieces of your health 
data, but not all of it. The lack of a unified view can 

2008

2009

2010

Free Cash Flow surpasses $100 million

Cerner Celebrates 30th Anniversary

Smart Semi, a mobile hospital room of  
the future, introduced and made 93 stops, 
hosting nearly 9,000 client attendees

Signed first agreement for the  
Cerner Smart Room™

Expanded footprint in Middle East with signing 
of Ministry of Health in United Arab Emirates

Signed first hosted client in France

Signed first client in Latin America

American Recovery & Reinvestment Act 
becomes law and includes $35 billion in 
incentives for the adoption of health care IT

First two Cerner ITWorks℠ contracts signed

Announced new mission statement, “To contribute to the systemic 
improvement of health care delivery and the health of communities”

Introduced HealtheIntent™ cloud-based platform

Patient Protection and Affordable Care Act becomes law  
in an effort to reform how health care is delivered in the U.S.

University of Missouri and Cerner create 
Tiger Institute for Health Innovation

Announced agreement with CareFusion to better integrate medical 
devices and electronic health records

Announced acquisition of IMC Health Care

Cerner clients connect with HHS and CDC 
to fight spread of influenza

Fisher-Titus Medical Center and Magruder Hospital partner with 
Cerner to become first all-digital, smart hospitals in the U.S.

First two Cerner RevWorks℠ contracts signed

Introduced uCern® platform and opened 
uCern Store

Cerner honored as one of the best employers for healthy lifestyles 
by The National Business Group on Health

Cerner added to NASDAQ 100 Index

Neal Patterson recognized by Forbes as one of “America’s Best-
Performing Bosses” for providing shareholders with the “biggest 
bang for the buck”

Cerner added to S&P 500 index

8,000 associates

2  Per a 2010 Practice Fusion survey conducted by GfK Roper.  

10

lead to missed opportunities for diagnosis, delays 
in treatment, waste of resources and excess costs 
due to repeated tests. 

The  absence  of  interoperability  in  health  care 
causes  a  significant  direct  and  added  burden 
on  sick  people  and  their  families,  who  are  left 
“holding  the  bag”—not  the  figurative  bag  of 
blame  (it  is  certainly  not  their  fault),  but  a  very 
real  bag  of  hundreds  of  printed  pages,  faxed 
records,  radiography  films  and  data  disks  they 
must  carry  between  doctor’s  visits.  My  wife 
Jeanne, a surviving cancer patient, has a bag like 
this....she actually has several of them. To further 
shed light on the problem, it’s typically only the 
better-resourced  and  proactive  patients 
like 
Jeanne who are able to assemble their records in 
the first place. That’s because each set of pages 
and  each  disk  in  the  bag  represents  a  visit  to  a 
records  department,  a  wait  at  an  information 
desk, or a phone call that was put on hold.

In the last few years, the term “data hoarding” has 
entered  the  health  care  lexicon.  A  data  hoarder 
is  any  person  or  organization  that  withholds  a 
person’s  health  data  for  competitive  reasons, 
stands  up  business  practices  that  disincentivize 
interoperability,  or  puts  up  other  unfair  barriers 
to  data  exchange.  Data  hoarding  occurs  when 
an  organization  is  able  to  share  data  but  makes 
business-related  choices  about  who  to  share 
with  and  how.  A  data  hoarder  can  be  a  provider 
organization;  it  can  also  be  a  health  IT  vendor.  I 
have  seen  provider  organizations  that  are  willing 
to  exchange  a  person’s  health  data  with  anyone 
but  the  competing  hospital  across  the  street.  I 

have also seen health IT vendors that will send a 
person’s data for free anywhere in the country as 
long as it stays on their proprietary platform, but 
will charge provider organizations a fee if the data’s 
destination is a competing health IT platform. 

In  some  industries,  you  might  chalk  this  kind  of 
behavior  up  to  shrewd  business  tactics.  Health 
care is different and should be different. In health 
care there is a self-evident ethical understanding 
that  a  person’s  health  data  belongs  to  the 
person  as  much  as  it  does  to  any  physician  or 
organization that holds it. For several years, this 
has been powerfully articulated using phrases like 
“Nothing  About  Me  Without  Me”  and  “Give  Me 
My Damn Data,” by everyone from patient rights 
activists like Dave DeBronkart and Regina Holliday 
to  health  reform  officials  like  Don  Berwick  and 
Suzanne  DelBanco.  At  the  national  policy  level, 
there is a movement to expose and penalize data 
hoarding practices wherever they occur.  

Health  care  data  is  different.  It  belongs  to  the 
person, and it also has different requirements and 
protections  under  the  law.  The  Health  Insurance 
Portability and Accountability Act of 1996 (HIPAA) 
made  it  illegal  to  share  personally  identifiable 
health  care  information  without  the  consent  of 
the  patient.  HIPAA  also  mandated  the  creation 
of  unique  national  patient  identifiers  (NPIs)  for 
U.S.  citizens,  a  move  that  could  have  greatly 
facilitated the kind of accurate patient matching 
needed  for  safe  nationwide 
interoperability. 
Two  years  later,  however,  Congress  prohibited 
funding  the  creation  of  NPIs  because  of  privacy 
concerns.  When  it  comes  to  exchanging  health 

2011

2012

2013

2 for 1 stock split (June 27)

Acquired Resource Systems  
(long-term care solutions)

Surpassed $3B in annual bookings, including over  
$1 billion in Q4

Announced $170 million Share Repurchase Program

2 for 1 stock split (July 1)

Annual bookings grew 20% to $3.8 billion

Total assets surpass $4 billion

Acquired Clairvia  
(workforce management solutions)

Revenue and bookings surpass $2 billion

Introduced new logo and tagline: Health 
care is too important to stay the same.™

Launched Cerner Skybox℠ suite of  
cloud services

Signed 1st Cerner QualityWorks℠ client

Cerner associates shed more than  
20,000 pounds during Slimdown  
Throwdown weight-loss competition

Cerner clients begin receiving stimulus 
funds related to achieving Meaningful Use

Acquisition of behavioral health company Anasazi Software

86% of clients attested or in process of attesting for  
Stage 1 Meaningful Use

Nearly double the number of client sites achieved HIMSS 
Analytics Electronic Medical Records Adoption Model℠  
Stage 6 or 7 in 2012 than our closest competitor;   
most stage 6 or 7 clients outside the U.S. as well

PowerChart+Touch™ went live at 13 early adopter clients

Advocate Health Care partnership led to more than  
20% improvement in ability to predict readmissions

Partnered with NBA to provide HealtheAthlete,® an  
organization-wide automated health care management system

Healthy Nevada project is creating a culture of health,  
digitizing health care and establishing integrated 
communication among all providers in the community

Completed $170 million Share Repurchase Program and 
announced another $217 million Share Repurchase Program

Announced partnership with Intermountain Healthcare for 
clinical systems, revenue cycle and population health  

Signed first client in Brazil, Hospital Israelita Albert Einstein

Acquisitions of wellness company PureWellness and 
laboratory automation company Labotix

Associates who manage and support our clients’ IT systems 
moved into new Continuous Campus facility 

Purchased 237 acres adjacent to Innovations Campus in 
Kansas City, MO, for long-term plan to add 15,000 associates

Released HealtheIntent Smart Registries℠ on Cerner’s  
cloud-based population health platform

#4 on Top 100 Healthiest Companies in America

#13 on Forbes list of World’s Most Innovative Companies, 
ahead of Google and Apple 

14,000 associates

11

data, the needs for privacy, security, accuracy and 
consumer control are real. It’s not easy to meet all 
of these obligations, but it is possible. 

A  few  years  ago,  the  head  of  the  Office  of  the 
Information 
National  Coordinator  for  Health 
Technology  implored  the  health  IT  industry  to 
come  together  to  provide  a  private  solution 
to  certain  problems  and  limitations  that  were 
hamstringing  progress  toward  interoperability. 
In  response,  Cerner  and  several  competitors 
co-founded  CommonWell  Health  Alliance,  an 
open,  not-for-profit  industry  consortium  that 
brings  health  IT  firms  together  for  the  purpose 
of enabling safe nationwide interoperability. The 
idea behind CommonWell is not to compete with 
federal policy, but to complement and accelerate it 
by providing solutions to three areas of weakness 
in the national standards: identity management, 
location  and  consent  management. 
record 
Through  CommonWell,  the  vendors  that  have 
profited  from  Meaningful  Use  come  together 
and  pay  a  fee  based  on  their  revenues  that 
provides  for  an  interoperability  infrastructure 
that  facilitates 
identity  management,  record 
location  and  consent  management  for  provider 
organizations  at  commodity  prices.  In  a  world 
where patients desperately need interoperability, 
CommonWell  is  a  practical,  market-led  way  to 
achieve  it  relatively  quickly,  especially  without 
any additional costs to taxpayers. 

When I started this letter, CommonWell members 
represented about 50% of the acute care market 
share. As we go to print, the number has increased 
to  70%.  It  needs  to  be  100%.  CommonWell 

has  completed  the  pilot  projects  phase  where 
members  tested  transactions  between  all  the 
different  vendors,  and  it  is  starting  to  sign  up 
health  care  provider  organizations  to  use  the 
service. It is a network, and we expect to see the 
“network effect” phenomenon where benefits are 
modest  and  perhaps  poorly  understood  at  first, 
but  greatly  increase  in  value  as  more  providers 
and consumers connect.  

The  one  vocal  opponent  of  CommonWell  is  a 
sizable health IT vendor that has used innuendo 
and  outright  misstatements  to 
imply  that 
CommonWell  is  a  “business”  with  a  hidden 
purpose  to  make  money  for  a  group  of  select 
interests. The detractor’s CEO has stated publicly 
that  she  believes  CommonWell  will  profit  from 
selling  personal  health  data.  The  truth  is  that 
CommonWell  is  not  a  business;  it’s  a  not-for-
profit. And CommonWell’s terms and conditions 
provide  CommonWell  with  no  data  rights  and 
prohibit  its  service  provider  from  selling  data. 
The  negative  statements  are  as  clear-cut  an 
example of FUD as I have ever seen. Interestingly, 
in  testimony  before  Senate  in  March  2015,  the 
same  company  expressed  no  misgivings  about 
the actual architecture of CommonWell and what 
it  does,  saying  “in  terms  of  what  they’re  doing, 
architecturally there’s not a problem with that.”3 

Other  industries  have  worked  together  to  solve 
this  type  of  problem.  The  banking  industry  did 
so around the creation of ATM networks. And, as 
nearly  everyone  knows,  today  you  can  open  an 
account  in  any  bank,  obtain  a  temporary  debit 
card, travel to another city or even country, and 

2014

Annual revenue grew 17% to $3.4 billion

Repurchased $217 million of stock  
under our Share Repurchase Program

Signed definitive agreement to purchase  
the Siemens Health Services business for 
$1.3 billion 

Cerner client Marina Salud became first  
non-U.S. hospital to earn HIMSS Davies 
Enterprise Award for demonstrating 
significant, sustainable improvement of 
patient outcomes through the utilization of 
an EHR and information technology while 
achieving return on investment

Cerner client Croydon Health Services NHS 
Trust in South London was recognized by 
HIMSS Europe as the first hospital in the UK 
to achieve Stage 6 certification

First place on Kansas City Business Journal’s 
list of Healthiest Employers for companies 
employing over 3,500 people

Cerner client Truman Medical Center honored 
with HIMSS Davies Enterprise Award and The 
College of Healthcare Information Management 
Executives (CHIME) – American Hospital 
Association (AHA) Transformational  
Leadership Award

CEO Neal Patterson recognized with Industry 
Leader Award by CHIME

Named to top 25 of Forbes list of World’s Most 
Innovative Companies

Named to Fortune magazine’s list of World’s 
Most Admired Companies and #1 Most Admired 
in Health Care industry

15,800 associates

3  Full Committee Hearing - America’s Health IT Transformation: Translating the Promise of Electronic Health Records Into Better Care, March 17, 2015.

12

use  your  card  to  safely  withdraw  money  from 
your  account  at  any  ATM  in  the  world,  even 
if  it  is  operated  by  a  competing  bank  with  no 
relationship  with  you  or  your  bank.  This  is  what 
we  are  trying  to  accomplish  with  CommonWell. 
The vision of CommonWell is for a patient to be 
able to visit a new doctor, give their consent, and, 
within  moments,  have  his  or  her  lifetime  record 
assemble from all the prior places he or she has 
visited. No one will be left holding the bag.  

The federal government is giving heavy scrutiny 
to  interoperability.  There  is  a  10-year  roadmap 
to  interoperability,  and  interop  is  a  major  focus 
of  Meaningful  Use  Stage  3  rulemaking  (with 
much  of  the  workload  appropriately  falling  on 
the  vendors).  Interoperability  will  happen.  It  is 
just now a matter of time. We hope and believe 
that CommonWell will play a big role in making it 
happen sooner versus later.

At  the  risk  of  providing  too  much  information 
on  this  subject,  one  final  note.  We  need  to 
go  beyond  simply  sending  data  between 
systems  for  review  by  the  providers  to  much 
involving  so-
more  sophisticated  scenarios 
called  “semantic  interoperability,”  where  data 
continually  flows 
in  machine-understandable 
format from one platform to another, where it can 
be consumed into intelligent workflows, just like 
information  that  is  native  to  that  system.  Today 
Cerner supports its clients who want to do point-
to-point  interfacing  and  connect  to  local  health 
information  exchanges,  but  we  are  working  to 
advance that universal “built in” connectivity. 

THE  BIGGEST  CHANGE  FACING  OUR  CLIENTS 
IS LOOMING

We  just  passed  the  five-year  anniversary  of  the 
Affordable Care Act (a.k.a. “Obamacare”), which 
has  created  the  biggest  decade  of  change  that 
health  care  has  ever  seen  in  the  U.S.  All  of  our 
clients  are  reacting  to  the  major  changes  in 
their  environments.  They  are  in  the  mode  to 
protect their current revenues, find new sources 
of  revenues,  improve  their  measurable  quality, 
and  prepare  themselves  for  risk  by  significantly 
reducing their cost of providing care. Many of the 
clients feel that they need to take 20% or more out 
of their cost and provide higher quality care. The 
biggest lever to do so is information technology. 

13

In the last year, we have engaged with a number 
of our longstanding clients to drive value creation 
and  process  improvement  initiatives  within  their 
organizations.  Each  long-term  engagement  has 
a  slightly  different  flavor,  depending  on  what  is 
most important to that client. We are steadfastly 
committed  to  creating  the  innovations  that  will 
help  them  deliver  the  best  care,  every  time,  to 
every  person,  and  at  the  lowest  attainable  cost. 
We are also committed to moving the boundaries 
of health care so that health systems can engage 
their communities in managing their health, right 
in  the  environments  where  they  live.  All  of  this, 
including  our  platform  for  helping  providers 
to  manage  population  health,  should  be  an 
important part of the next phase of Cerner. 

Despite  the  fact  that  the  last  several  years 
have  brought  profound  changes,  the  biggest 
change of all is yet to come. Barring unforeseen 
circumstances, I believe it will get here in the next 
three years. I am talking about a change in how 
doctors,  hospitals  and  other  providers  get  paid. 
For the past 100 years, fee-for-service (FFS) has 
been  the  core  method  for  commerce  in  health 
care.  The  more  services,  the  more  fees.  The  ills 
of  fee-for-service  have  been  well  publicized;  I’m 
not  going  to  rehash  them  all  here.  The  biggest 
issue  with  FFS  is  a  misalignment  of  incentives. 
The  only  way  for  physicians  and  hospitals  to 
get paid is for you to become sick and for them 
to  do  things  for  you.  No  one  is  getting  paid  to 
keep  you  well,  and  the  act  of  paying  providers 
and hospitals for every procedure and treatment, 
rather than outcomes, produces exactly what you 
think  it  would  produce—volumes  of  procedures 
and 
to 
outcomes. I don’t think that FFS was “designed” 
to produce the outcomes it produces. Physicians 
and  hospitals  do  very  specialized  work,  and  it 
is  important  for  them  to  be  fairly  compensated 
for their years of education and their work. It is a 
blessing that they are there when the need is the 
greatest (when you are sick), but there is also no 
doubt that the system itself creates no incentive 
to keep people healthy and out of doctor’s offices 
and hospitals. On the contrary, most of the time, 
the  system  will  not  pay  physicians  for  e-visits, 
telemedicine  visits,  and  other  technology-based 
delivery  that  would  save  time  and  resources, 
help  prevent  avoidable  complications,  and  add 

treatments,  with 

little  correlation 

convenience. If you want to read more about FFS, 
there  have  been  plenty  of  eye-opening  articles 
on  the  subject,  from  Atul  Gawande’s  2009  New 
Yorker  piece  on  the  high  cost  of  health  care  in 
McAllen, Texas, to Haley Sweetland Edwards’ 2013 
article  in  Washington  Monthly  about  the  “RUC.” 
On a thirty-year cycle, there have been attempts 
to introduce new methods of payment, including 
a  significant  effort  in  1986  with  the  introduction 
of DRGs. It has been 30 years since the last major 
effort to change. 

This  is  the  decade  that  many  believe  will  see 
the  end  of  FFS,  or  at  least  its  diminution  to  a 
lesser-used  model  of  payment.  The  lever  for 
this  change  will  be  the  Centers  for  Medicare 
and  Medicaid  Services  (CMS),  which  pays  more 
than  50%  of  medical  bills  in  the  U.S.  In  January 
of  2015,  HHS  Secretary  Sylvia  Burwell  laid  out 
a  plan  to  shift  50%  of  Medicare  payments  to 
value-based payment models by the end of 2018, 
and  to  tie  90%  of  the  remaining  traditional  FFS 
payments to quality measures. Tying payment to 
health outcomes is going to produce some really 
massive shifts in the way health care is provided 
in  the  next  decade.  You  will  see  a  greater  focus 
on patient engagement, wellness and prevention, 
and  the  locus  of  health  and  care  will  shift  away 
from  high-cost  venues  like  hospitals  and  into 
lower-cost venues like the home.  

Health  care  providers  and  health  systems 
are  already  actively  experimenting  with  risk-
based,  value-based,  bundled  payment  models 
in  an  attempt  to  prepare  for  the  shift  toward 
Accountable  Care  Organizations  that  many 
see  as  inevitable.  What  few  people  outside  of 
health  care  seem  to  know  is  that  most  health 
care provider organizations do not actually know 
how much it costs to provide the care they give 
to you. How much they are paid for a particular 
procedure is largely determined by forces outside 
of their control, and there is also a great deal of 
cost-shifting  that  occurs  between  Medicare  and 
Medicaid patients, insured patients and uninsured 
patients. As provider organizations go more “at-
risk”  for  the  outcomes  within  their  populations, 
they  will  have  an  increased  need  to  understand 
their  own  costs  and  control  them  relative  to 
outcomes. I’m very excited that one of the focuses 
of our relationship with Intermountain Healthcare is 

to produce a true Activity-Based Costing system 
for  health  care.  In  addition  to  implementing 
existing Intermountain Care Process Models and 
Clinical Process Guidelines inside their workflows, 
we  have  done  preliminary  work  on  this  system 
with 
Intermountain’s  Chief  Quality  Officer  
Dr.  Brent  James,  who  is  widely  regarded  as 
an  expert  in  the  subject.  As  health  care  heads 
toward a new era of performance-based payment 
models, it couldn’t come at a better time. 

A CO-FOUNDER RETIRES

We  started  Cerner  35  years  ago  as  three 
twentysomethings—Cliff  Illig,  Paul  Gorup  and 
myself—sitting  around  a  park  bench  during  the 
summer  of  1979,  dreaming  out  loud....if  we  were 
to  start  a  company,  what  industry  would  we  set 
out  to  change?  Back  then  when  someone  said 
the  words  information  technology,  they  were 
talking  about  hardware.  We  started  our  careers 
“writing code” (software) working as information 
systems  consultants.  We  had  seen  just  enough 
to  intuit  that  software  was  the  real  value  in  the 
stack  of  information  technology.  We  wanted  to 
start  our  company  at  the  operational  side  of  an 
organization,  not  just  automating  back  office 
administrative  functions.  Although  at  first  we 
didn’t  know  exactly  what  we  wanted  to  do,  we 
made  a  list  of  characteristics  the  right  industry 
should have. It should be in a vertical market with 
specialized  needs.  It  should  be  highly  complex. 
Ideally  it  would  be  an  industry  with  a  strong 
need for standardization. And it needed to be an 
industry where information played a very big role. 
In short, we wanted to be an application software 
company  that  automated  the  mission-critical 
industry. 
processes  of  an 
When  we  found  our  first  health  care  client,  it 
was a little bit like finding your dream date. The 
bonus was that health care also turned out to be 
important,  exciting,  and  intensely  personal.  The 
entrepreneurial  idea  turned  into  a  true  calling. 
Since  that  discovery,  our  work  has  been  about 
connecting what matters. 

information-driven 

Although  it’s  a  fairly  common  story  today,  in 
the late ‘70s, there were not a lot of people our 
age starting companies. This year we are hitting 
another milestone, with Paul Gorup retiring. On the 
road to building Cerner, each of the founders has 

14

played a critical role. One way for me to describe 
Paul’s  enormous  contribution  is  the  way  I  have 
introduced him from day one: he is the smartest 
of the three of us. Those who know us well have 
no  doubt.  He  is  simply  brilliant,  adapting  his 
intelligence to create architectures, technologies 
and solutions for health care. The other way is to 
state the title he has had in the company for the 
last decade, Chief of Innovation. Paul is one of the 
most creative, passionate people you could hope 
to meet, certainly at Cerner and possibly in all of 
health information technology. Paul will continue 
to work with us for the remainder of this decade 
in  a  couple  of  areas,  but  his  grandkids  are  now 
going to see much more of him. I am grateful for 
the opportunity to create and grow this company 
with Paul. 

The  founders’  strengths  have  helped  determine 
the  core  Cerner  attributes  of  vision,  innovation 
and  culture.  A  more  wondrous  thing  is  how,  at 
some point, the attributes have become imprinted 
on the organization. Today I see Cliff in associates 
who have never met Cliff, Paul in associates who 
have never met Paul. Even though Paul is retiring, 
he will still be here. 

CONCLUSION—IN THE LONG TERM

The  interesting  thing  about  the  future  is  that  it 
quickly becomes the present, and then, in a flash, 
it is our past. At Cerner we have always believed 
in  keeping  our  vision  of  the  future  as  our  daily 
guidepost. A regular question for our executives 
is, are you getting dominated by the “windshield” 
of  present  demands,  or  are  you  also  working 
on  what’s  next?  A  quick  glance  back  gives  us 
reinforcement that these principles are rewarding. 
As  CEO  for  all  of  these  years,  I  am  somewhat 
plagued  by  thoughts  about  mistakes  we  made 
and  how  much  better  we  could  have  been. 
Despite our very human journey, we continue to 
be  at  a  great  place—the  intersection  of  health 
care and information technology—with discipline 
around vision, a great culture, and an instinct to 
innovate. If we keep our focus on creating value 
for  our  clients,  and  if  we  keep  redefining  the 
boundaries,  it  is  highly  probable  that  our  vision, 
innovation and culture will be rewarded well into 
the future. Thank you for the role you play in the 
Cerner journey.

Sincerely,

NEAL L. PATTERSON
Chairman, Chief Executive Officer  
& Co-founder

15

Appendix:  
Reconciliation of 2014 Non-GAAP Results to GAAP Results*

($ in millions except Earnings Per Share)

GAAP Operating Earnings

Share-based compensation expense

Adjustments related to acquisition of Siemens Health Services

Operating  
Earnings

Operating  
Margin %

$763

22.4%

63

16

Adjusted Operating Earnings (non-GAAP)

$842

24.7%

GAAP Net Earnings

Share-based compensation expense, net of tax

Adjustments related to acquisition of Siemens Health Services,  
net of tax

Net  
Earnings

Diluted 
Earnings  
Per Share

$525

41

10

$1.50

0 .12

0 .03

Adjusted Net Earnings (non-GAAP)

$576

$1.65

GAAP Operating Cash Flow

Capital purchases

Capitalized software development costs

Free Cash Flow (non-GAAP)

$847

(276)

(178)

$393

* More detail on these adjustments and management’s use of Non-GAAP results is in our 2014 annual 
report on Form 10-K and our current reports on Form 8-K .

16

Cerner Corporation 
2014 Annual Report
Form 10-K

Table of Contents

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

FORM 10-K

(X) 

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

1934

For the fiscal year ended: January 3, 2015   

OR

(  ) 

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

OF 1934

For the transition period from ___________ to ___________

Commission File Number: 0-15386

CERNER CORPORATION
(Exact name of registrant as specified in its charter)

Delaware
(State or other jurisdiction of
incorporation or organization)

2800 Rockcreek Parkway 
North Kansas City, MO
(Address of principal executive offices)

43-1196944
(I.R.S. Employer Identification
Number)

64117
(Zip Code)

(816) 201-1024
(Registrant's telephone number, including area code)

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

Title of each class
Common Stock, $0.01 par value per share

   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 [X]     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 [X]

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the 
Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was 
required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.

Yes [X]     No [  ]

18

 
 
 
 
Table of Contents

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, 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 [X]     No [  ]

Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K (§229.405 of this chapter) 
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. [X]

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.

Large accelerated filer [X]     Accelerated filer [  ]     Non-accelerated filer [  ]     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 [X]

As of June 28, 2014, the aggregate market value of the registrant’s common stock held by non-affiliates of the registrant 
was $15.5 billion based on the closing sale price as reported on the NASDAQ Global Select Market. 

Indicate the number of shares outstanding of the issuer’s classes of common stock, as of the latest practicable date.

Class
Common Stock, $0.01 par value per share

Outstanding at February 6, 2015
342,588,295 shares

DOCUMENTS INCORPORATED BY REFERENCE

Document
Proxy Statement for the Annual Shareholders'
Meeting to be held May 22, 2015

Parts into Which Incorporated
Part III

19

  
  
  
  
Table of Contents

PART I.

Item 1. Business

Overview
Cerner Corporation started doing business in 1980, and it was organized as a Delaware corporation in 1986. Unless the 
context otherwise requires, references in this report to “Cerner,” the “Company,” “we,” “us” or “our” mean Cerner Corporation 
and its subsidiaries. 

Our corporate world headquarters is located in a Company-owned office park in North Kansas City, Missouri, with our principal 
place  of  business  located  at  2800  Rockcreek  Parkway,  North  Kansas  City,  Missouri  64117.  Our  telephone  number  is 
816.201.1024.  Our  Web  site,  which  we  use  to  communicate  important  business  information,  can  be  accessed  at: 
www.cerner.com. We make our annual report on Form 10-K, quarterly reports on Form 10-Q, current reports on Form 8-K 
and all amendments to those reports available free of charge on or through this Web site as soon as reasonably practicable 
after such material is electronically filed with or furnished to the Securities and Exchange Commission (SEC).

Cerner is a leading supplier of health care information technology (HCIT).  Our mission is to contribute to the improvement 
of health care delivery and the health of communities.  We offer a wide range of intelligent solutions and services that support 
the clinical, financial and operational needs of organizations of all sizes.  We have systems in more than 18,000 facilities 
worldwide,  including  hospitals,  physician  practices,  laboratories,  ambulatory  centers,  behavioral  health  centers,  cardiac 
facilities, radiology clinics, surgery centers, extended care facilities, retail pharmacies, and employer sites.

Cerner solutions are offered on the unified Cerner Millennium® architecture and on the HealtheIntent™ cloud-based platform.  
Cerner Millennium is a person-centric computing framework, which includes integrated clinical, financial and management 
information systems. This architecture allows providers to securely access an individual’s electronic health record (EHR) at 
the point of care, and it organizes and proactively delivers information to meet the specific needs of physicians, nurses, 
laboratory technicians, pharmacists, front- and back-office professionals and consumers.  Our HealtheIntent platform is a 
cloud-based platform that enables a new generation of solutions to leverage the increasing amount of data being captured 
as the health care industry is digitized. On the HealtheIntent platform, we offer EHR-agnostic solutions based on sophisticated, 
statistical algorithms that are intended to help providers predict and improve outcomes, control costs, improve quality, and 
manage the health of the populations they serve. 

We offer a broad range of services, including implementation and training, remote hosting, operational management services, 
revenue  cycle  services,  support  and  maintenance,  health  care  data  analysis,  clinical  process  optimization,  transaction 
processing, employer health centers, employee wellness programs and third party administrator (TPA) services for employer-
based health plans. 

In addition to software and services, we offer a wide range of complementary hardware and devices, both directly from Cerner 
and as a reseller for third parties. 

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The following table presents our consolidated revenues by major solutions and services and by segment, as a percentage 
of total revenues: 

Revenues by Solutions & Services

System sales

Support and maintenance

Services

Reimbursed travel

Revenues by Segment

Domestic

Global

For the Years Ended

2014

2013

2012

28%
21%
48%
3%

100%

89%
11%
100%

29%

23%

46%
2%
100%

34%

23%

41%

2%

100%

88%

12%

88%

12%

100%

100%

Health Care and Health Care IT Industry 
There are several trends in health care that we believe create a favorable environment for Cerner. One is the unsustainable 
rate of growth in health care spending. The Centers for Medicare and Medicaid Services (CMS) estimates United States 
health care spending in 2014 at $3.1 trillion, or 17.6 percent of Gross Domestic Product (GDP), and projects it to be 19.3 
percent of GDP by 2023. We believe health care IT is one of few remaining levers that can change this trajectory.  Further, 
health care providers continue to operate in an environment that includes what we call ‘raining measures and mandates’.  
Examples of these include: 

•  Health Information Technology for Economic and Clinical Health (HITECH) provisions within the American Recovery 
and Reinvestment Act (ARRA) that offer incentives for health care organizations to modernize operations through 
“Meaningful Use” of HCIT and will begin to penalize for non-compliance in coming years;

•  Value-Based Purchasing programs that link reimbursement to quality and outcomes;
• 
•  Readmission reduction programs that penalize hospitals for unnecessary readmissions.

Increasing requirements to report quality metrics; and

Collectively, these measures and mandates are driving providers to focus on delivering higher quality care at a lower cost, 
and we believe HCIT is a key lever that can help providers accomplish this. We also believe all of these shifts are leading to 
an environment in which health care providers will become accountable for proactively managing the health of the populations 
they serve, and this will require ongoing investment in sophisticated information technology solutions that will enable them 
to predict when intervention is needed so they can improve outcomes and lower the cost of providing care.

As providers position themselves for these shifts, there has been an increase in industry consolidation, with health systems 
acquiring hospitals, physician practices, and other venues to control more of the care continuum and achieve economies of 
scale.  We believe this is a positive trend for Cerner as we have relationships with the majority of the largest health systems 
responsible for most of the acquisition activity, creating an opportunity to offer our solutions and services to the acquired 
facilities.

The increasingly complex and more clinical outcomes-based reimbursement environment is also contributing to a heightened 
demand for revenue cycle solutions and a desire for these solutions to be closely aligned with clinical solutions.  We believe 
this trend is positive for Cerner because our revenue cycle solutions are integrated with our clinical solutions, creating a 
clinically driven revenue cycle solution that has had significant adoption in recent years.

We have also seen a shift in the United States marketplace towards a preference for a single platform across inpatient and 
ambulatory settings. The number of physicians employed by hospitals has increased significantly as hospitals have acquired 
physician groups in order to ensure a consistent stream of referrals, and health systems are recognizing the benefit of having 
a single patient record at the hospital and the physician office. We are benefiting from this trend due to our unified Cerner 
Millennium platform that spans multiple venues and due to significant enhancements we have made to our physician solutions 
in recent years.

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Outside the United States, we believe Cerner’s growth opportunities are good as most countries are also dealing with health 
care expenditures growing faster than their economies, which is leading to a focus on controlling costs while also improving 
quality of care. 

Cerner Vision and Growth Strategy 
For over three decades, Cerner has been continuously building intelligent solutions for the health care industry. Together 
with our clients, we are creating a future where the health care system works to improve the well-being of individuals and 
communities. Our vision has always guided our large investments in research and development (R&D), which have created 
strong levels of organic growth throughout our history.  Our proven ability to innovate has led to what we believe to be industry-
leading solution and device architectures and an unmatched breadth and depth of solutions and services.  The strength of 
our solutions and services has led to our ability to gain market share in recent years, which has contributed to our growth.  
We  believe  we  are  positioned  to  continue  gaining  share  in  coming  years  as  regulatory  requirements  and  industry  shifts 
continue to pressure health care providers to improve quality while lowering costs, which will require having more sophisticated 
information technology than many of our competitors provide. 

In addition to growth by gaining market share, we have a significant opportunity to grow revenues by expanding our solution 
footprint with existing clients. There is opportunity to expand penetration of our core solutions, such as EHRs and computerized 
physician order entry, and increase penetration of our broad range of complementary solutions that can be offered into our 
existing client base. Examples include women’s health, anesthesiology, imaging, clinical process optimization, critical care, 
health care devices, device connectivity, emergency department, revenue cycle and surgery. 

We also have an opportunity to grow by expanding penetration of services we offer that are targeted at capturing a larger 
percentage of our clients’ existing IT spending. These services leverage our proven operational capabilities and the success 
of our CernerWorksSM managed services business, where we have demonstrated the ability to improve our clients’ service 
levels at a cost that is at or below amounts they were previously spending. One of these services is Cerner ITWorksSM, a 
suite of solutions and services that improve the ability of hospital IT departments to meet their organization’s needs while 
also creating a closer alignment between Cerner and our clients. A second example is Cerner RevWorksSM, which includes 
solutions and services to help health care organizations improve their revenue cycle functions. 

We have made progress over the past several years at reducing the total cost of our solutions, which expands our end market 
opportunities by allowing us to offer lower-cost, higher-value solutions and services to smaller community hospitals, critical 
access hospitals and physician practices. For example, our CommunityWorksTM offering leverages a shared instance of the 
Cerner Millennium platform across multiple clients, which decreases the total cost for these clients. 

We also expect to drive growth over the course of the next decade through initiatives outside the core HCIT market. For 
example, we offer clinic, pharmacy, wellness and third-party administrator services directly to employers. These offerings 
have been shaped by what we have learned from changes we have implemented at Cerner. We have removed our third-
party  administrator  and  become  self-administered,  launched  an  on-site  clinic  and  pharmacy,  incorporated  biometric 
measurements for our population, realigned the economic incentives for associates in our health plan, and implemented a 
data-driven wellness management program. These changes have had a positive impact on the health of our associates while 
also reducing our health care costs. 

As discussed below, another opportunity for future growth, and a significant area of investment for Cerner, is leveraging the 
vast amounts of data being created as the health care industry is digitized and using this data to help providers manage the 
health of populations. 

Population Health
We believe Population Health Management is more than an industry buzzword or the next big fad.  It is the shift from solely 
automating  health  systems  to  managing  a  person’s  health.  Getting  there  requires  complete,  accurate  patient  data  and 
meaningfully  using  that  data  to  engage  individuals,  exchange  information  between  providers  and  ultimately  drive  better 
outcomes. This shift will shape the future of health care and enable a system driven by accountability, transparency and 
value.

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Cerner's approach to population health is to enable organizations to:

•  KNOW what is happening and predict what will happen within their population through solutions for data exchange, 

longitudinal record, enterprise data warehouse, analytics and quality and regulatory reporting;

•  ENGAGE providers and patients in health and care delivery through personal health portals and solutions for care 

management, home care, long-term care, and retail pharmacy; and

•  MANAGE health and improve care with capacity and workforce management, clinical research, predictive modeling, 

health registries, and contract and network management.

These solutions are enabled by Cerner’s HealtheIntent platform, which is a multi-purpose, programmable platform designed 
to scale at a population level while facilitating health and care at a person and provider level.  This cloud-based platform 
enables organizations to aggregate, transform and reconcile data across the continuum of care, and helps improve outcomes 
and lower costs.

HealtheIntent is scalable, secure and can be accessed anywhere, anytime. It is able to receive data from any EHR, existing 
HCIT system and other data sources, such as pharmacy benefits managers or insurance claims. HealtheIntent collects data 
from multiple, disparate sources in near real-time, providing clarity to millions of data points in an actionable and programmable 
workflow. It enables organizations to identify, score and predict the risks of individual patients, allowing them to match the 
right care programs to the right individuals.  The EHR-agnostic nature of our HealtheIntent platform allows us to offer our 
solutions to the entire marketplace, not just existing Cerner clients.

We are investing heavily in expanding the HealtheIntent platform and our overall capabilities to support population health.  
One of the ways we are expanding our capabilities is working closely with clients that are early movers at taking accountability 
for keeping the populations they serve healthy.  A key partner with whom we are working is Advocate Health Care ("Advocate").  
One of the first outcomes of this collaboration was the joint development in 2012 of a predictive agent for readmissions that 
has demonstrated significant improvement in predictive power as compared to the majority of existing models.  Our relationship 
expanded in early 2013 to further advance clinical integration and population health management capabilities across the 
continuum of care for the more than 500,000 lives for which they have gone at risk.

In September 2013, we released HealtheRegistries™, which provides the ability to stratify patient populations based on risk, 
conditions, and attributed physicians.  Advocate went live with HealtheRegistries in January 2014 and we have since sold 
the solution to multiple clients.  In 2014, we continued to advance our population health capabilities through our work with 
Advocate, including development of care management solutions that we expect to release in 2015 and a transition of care 
model that suggests 30 percent of the population could be sent to a more optimal venue and achieve better outcomes at a 
lower cost.

In summary, we believe our comprehensive architectural approach to population health is differentiated in the marketplace.  
We expect population health to be a large contributor to our long-term growth as health care continues to evolve towards a 
model that incents keeping people healthy.  

Siemens Health Services Acquisition
On February 2, 2015, we acquired substantially all of the assets, and assumed certain liabilities of Siemens AG's health 
information technology business unit, Siemens Health Services. We believe our acquisition of Siemens Health Services 
enhances our organic growth opportunities discussed above.  The acquisition provides a larger base into which we can sell 
our broad range of solutions and services, with opportunities ranging from selling Cerner’s EHR into the Siemens Health 
Services client base, to selling EHR-agnostic solutions such as population health, to selling services such as RevWorks and 
ITWorks.  The acquisition also augments our non-U.S. growth opportunities, increases our ability to continue investing in 
R&D, and adds thousands of highly-skilled associates that will enhance Cerner’s capabilities.

Software Development 
We commit significant resources to developing new health information system solutions and services. As of the end of 2014, 
approximately 4,300 associates were engaged in research and development activities. Total expenditures for the development 
and enhancement of our software solutions were approximately $467.2 million, $418.7 million and $319.8 million during the 
2014, 2013 and  2012  fiscal  years,  respectively. These  figures  include  both  capitalized  and  non-capitalized  portions  and 
exclude amounts amortized for financial reporting purposes. 

As  discussed  above,  continued  investment  in  R&D  remains  a  core  element  of  our  strategy.  This  will  include  ongoing 
enhancement of our core solutions and development of new solutions and services. 

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Sales and Marketing 
The markets for Cerner HCIT solutions, health care devices and services include integrated delivery networks, physician 
groups and networks, managed care organizations, hospitals, medical centers, free-standing reference laboratories, home 
health agencies, blood banks, imaging centers, pharmacies, pharmaceutical manufacturers, employers, governments and 
public health organizations. The majority of our sales are sales of clinical and revenue cycle solutions and services to hospitals 
and health systems, but our solutions and services are highly scalable and sold to organizations ranging from physician 
practices,  to  community  hospitals,  to  complex  integrated  delivery  networks,  to  local,  regional  and  national  government 
agencies. 

Sales to large health systems typically take approximately nine to 18 months, while the sales cycle is often shorter when 
selling to smaller hospitals and physician practices. In some instances, the HITECH provisions of ARRA have shortened the 
sales process due to the timeline required for hospitals to qualify for stimulus incentives. 

Our  executive  marketing  management  is  located  at  our  Innovation  Campus  in  Kansas  City,  Missouri,  while  our  client 
representatives are deployed across the United States and globally. In addition to the United States, through our subsidiaries, 
we have sales associates and/or offices giving us a presence in more than 25 countries. 

We support our sales force with technical personnel who perform demonstrations of Cerner solutions and services and assist 
clients in determining the proper hardware and software configurations. Our primary direct marketing strategy is to generate 
sales contacts from our existing client base and through presentations at industry seminars and tradeshows. We market the 
PowerWorks®  solutions,  offered  on  a  subscription  basis,  directly  to  the  physician  practice  market  using  lead  generation 
activities and through existing acute care clients that are looking to extend Cerner solutions to affiliated physicians. We attend 
a  number  of  major  tradeshows  each  year  and  sponsor  executive  user  conferences,  which  feature  industry  experts  who 
address the HCIT needs of large health care organizations. 

Client Services 
Substantially  all  of  Cerner’s  clients  that  buy  software  solutions  also  enter  into  software  support  agreements  with  us  for 
maintenance and support of their Cerner systems.  In addition to immediate software support in the event of problems, these 
agreements allow clients to access new releases of the Cerner solutions covered by support agreements.  Each client has 
24-hour access to the client support team located at our world headquarters in North Kansas City, Missouri, our Continuous 
Campus in Kansas City, Kansas and our global support organizations in England and Ireland. 

Most  clients  who  buy  hardware  through  Cerner  also  enter  into  hardware  maintenance  agreements  with  us.  These 
arrangements normally provide for a fixed monthly fee for specified services.  In the majority of cases, we utilize subcontractors 
to  meet  our  hardware  maintenance  obligations.  We  also  offer  a  set  of  managed  services  that  include  remote  hosting, 
operational management services and disaster recovery. 

Backlog 
At the end of 2014, we had a revenue backlog of $10.6 billion, which compares to $8.9 billion at the end of 2013. Such 
backlog represents contracted revenue that has not yet been recognized. We estimate that approximately 27 percent of the 
backlog at the end of 2014 will be recognized as revenue during 2015. 

Competition 
The market for HCIT solutions, devices and services is intensely competitive, rapidly evolving and subject to rapid technological 
change. Our principal competitors in the health care solutions and services market include, but are not limited to: Allscripts 
Healthcare  Solutions,  Inc.,  Computer  Programs  and  Systems,  Inc.  (CPSI),  Epic  Systems  Corporation,  GE  Healthcare 
Technologies, Healthland, Inc., McKesson Corporation, MEDHOST, Inc. and Medical Information Technology, Inc., each of 
which offers a suite of software solutions that compete with many of our software solutions and services. 

Other competitors focus on only a portion of the market that we address. For example, such competitors include, without 
limitation,  Clinovations,  Inc.,  Dell,  Inc.  (Dell),  Deloitte  Consulting  LLP  (Deloitte),  Encore  Health  Resources,  LLC,    IBM 
Corporation (IBM), Impact Advisors, LLC and Xerox Corporation Ltd., which offer HCIT services that compete directly with 
some  of  our  service  offerings. AmazingCharts.com,  Inc., Athenahealth,  Inc.,  eClinicalWorks  LLC,  e-MDs,  Inc.,  Netsmart 
Technologies, Practice Fusion, Inc., Quality Systems, Inc., SRSsoft and Vitera Healthcare Solutions offer solutions to the 
physician practice market or niche market, but do not currently have a significant presence in the broader health systems 
and independent hospital market. 

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Cerner partners with third parties as a reseller of devices and markets its own competing proprietary health care devices. 
We view our principal competitors in the health care device market to include, without limitation: Aesynt Inc., CapsuleTech, 
Inc., CareFusion Corporation, Connexall Company, Ltd., Nanthealth, LLC, Omnicell, Inc., PerfectServe, Inc., Siemens AG 
and Vocera Communication, Inc. We view our principal competitors in the health care revenue cycle market to include, without 
limitation: Accretive Health, Inc., Conifer Health Solutions, Dell, Deloitte, Emdeon Corporation, MedAssets, Inc., Optum, Inc. 
(Optum), Quadramed Corporation, SSI Group, Inc. and 3M Company. We view our competitors in the population health 
market to range from small niche competitors, to large health insurance companies including, without limitation: Aetna Inc., 
Evolent Health, LLC, Explorys, Inc., IBM, MedeAnalytics, Inc., NetOrange, Inc., Optum, Phytel, Inc., The Advisory Board 
Company, and WellCentive, Inc.  Some of these competitors are larger or have more experience in their respective markets.

In addition, we expect that major software information systems companies, large information technology consulting service 
providers  and  system  integrators,  start-up  companies,  managed  care  companies,  healthcare  insurance  companies, 
accountable care organizations and others specializing in the health care industry may offer competitive software solutions, 
devices or services. The pace of change in the HCIT market is rapid and there are frequent new software solutions, devices 
or services introductions, enhancements and evolving industry standards and requirements. We believe that the principal 
competitive factors in this market include the breadth and quality of solution and service offerings, the stability of the solution 
provider, the features and capabilities of the information systems and devices, the ongoing support for the systems and 
devices and the potential for enhancements and future compatible software solutions and devices. 

Number of Employees (Associates)
At the end of 2014, we employed approximately 15,800 associates worldwide. 

Operating Segments 
Information about our operating segments, which are geographically based, may be found in Item 7 “Management’s Discussion 
and Analysis of Financial Condition and Results of Operations” below and in Note (19) to the consolidated financial statements. 

Executive Officers of the Registrant 
The following table sets forth the names, ages, positions and certain other information regarding the Company’s executive 
officers as of February 6, 2015. Officers are elected annually and serve at the discretion of the Board of Directors. 

Name
Neal L. Patterson

Age
65

Positions
Chairman of the Board of Directors and Chief Executive Officer

Clifford W. Illig

Zane M. Burke

Marc G. Naughton

Michael R. Nill

Randy D. Sims

Jeffrey A. Townsend

Julia M. Wilson

64

49

59

50

54

51

52

Vice Chairman of the Board of Directors

President

Executive Vice President and Chief Financial Officer

Executive Vice President and Chief Operating Officer

Senior Vice President, Chief Legal Officer and Secretary

Executive Vice President and Chief of Staff

Executive Vice President and Chief People Officer

Neal L. Patterson, co-founder of the Company, has been Chairman of the Board of Directors and Chief Executive Officer of 
the Company for more than five years. Mr. Patterson served as President of the Company from July 2010 to September 
2013, which position he also held from March of 1999 until August of 1999. 

Clifford W. Illig, co-founder of the Company, has been a Director of the Company for more than five years. He previously 
served as Chief Operating Officer of the Company until October 1998 and as President of the Company until March of 1999. 
Mr. Illig was appointed Vice Chairman of the Board of Directors in March of 1999. 

Zane  M.  Burke  joined  the  Company  in  September  1996.  Since  that  time,  he  has  held  a  variety  of  client-facing  sales, 
implementation  and  support  roles,  including  Corporate  Controller  and  Vice  President  of  Finance.  He  was  promoted  to 
President of the Company’s West region in 2002 and Senior Vice President of National Alignment in 2006. He was further 
promoted to Executive Vice President - Client Organization in July 2011 and to President of the Company in September 
2013.

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Marc G. Naughton joined the Company in November 1992 as Manager of Taxes. In November 1995 he was named Chief 
Financial Officer and in February 1996 he was promoted to Vice President. He was promoted to Senior Vice President in 
March 2002 and promoted to Executive Vice President in March 2010. 

Michael R. Nill joined the Company in November 1996. Since that time he has held several positions in the Technology, 
Intellectual Property and CernerWorks Client Hosting Organizations. He was promoted to Vice President in January 2000, 
promoted to Senior Vice President in April 2006 and promoted to Executive Vice President and named Chief Engineering 
Officer in February 2009. Mr. Nill was appointed Chief Operating Officer in May 2011. 

Randy D. Sims joined the Company in March 1997 as Vice President and Chief Legal Officer and was promoted to Senior 
Vice President in March 2011. Prior to joining the Company, Mr. Sims worked at Farmland Industries, Inc. for three years 
where he last served as Associate General Counsel. Prior to Farmland, Mr. Sims was in-house legal counsel at The Marley 
Company for seven years, holding the position of Assistant General Counsel when he left to join Farmland. 

Jeffrey A. Townsend joined the Company in June 1985. Since that time he has held several positions in the Intellectual 
Property Organization and was promoted to Vice President in February 1997. He was appointed Chief Engineering Officer 
in March 1998, promoted to Senior Vice President in March 2001, named Chief of Staff in July 2003 and promoted to Executive 
Vice President in March 2005. 

Julia M. Wilson first joined the Company in July 1990. Since that time, she has held several positions in the Functional Group 
Organization. She was promoted to Vice President and Chief People Officer in August 2003, to Senior Vice President in 
March 2007 and to Executive Vice President in March 2013. 

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Item 1A. Risk Factors

Risks Related to our Business 

We may incur substantial costs related to product-related liabilities. Many of our software solutions, health care devices 
or services (including life sciences/research services) are intended for use in collecting, storing and displaying clinical and 
health care-related information used in the diagnosis and treatment of patients and in related health care settings such as 
admissions, billing, etc. We attempt to limit by contract our liability; however, the limitations of liability set forth in the contracts 
may not be enforceable or may not otherwise protect us from liability for damages. We may also be subject to claims that 
are not covered by contract. Although we maintain liability insurance coverage, there can be no assurance that such coverage 
will cover any particular claim that has been brought or that may be brought in the future, that such coverage will prove to 
be adequate or that such coverage will continue to remain available on acceptable terms, if at all. A successful material claim 
or series of claims brought against us, if uninsured or under-insured, could materially harm our business, results of operations 
and financial condition. Product-related claims, even if not successful, could damage our reputation, cause us to lose existing 
clients, limit our ability to obtain new clients, divert management’s attention from operations, result in significant revenue 
loss, create potential liabilities for our clients and us and increase insurance and other operational costs. 

We may be subject to claims for system errors and warranties. Our software solutions and health care devices are very 
complex  and  may  contain  design,  coding  or  other  errors,  especially  when  first  introduced.  It  is  not  uncommon  for  HCIT 
providers to discover errors in software solutions and/or health care devices after their introduction to the market.  Similarly, 
the  installation  of  our  software  solutions  and  health  care  devices  is  very  complex  and  errors  in  the  implementation  and 
configuration of our systems can occur.  Our software solutions and health care devices are intended for use in collecting, 
storing, and displaying clinical and health care-related information used in the diagnosis and treatment of patients and in 
related health care settings such as admissions, billing, etc. Therefore, users of our software solutions and health care devices 
have  a  greater  sensitivity  to  errors  than  the  market  for  software  products  and  devices  generally.  Our  client  agreements 
typically provide warranties concerning material errors and other matters. Should a client’s Cerner software solution or health 
care device fail to meet these warranties or lead to faulty clinical decisions or injury to patients, it could 1) constitute a material 
breach under the client agreement, allowing the client to terminate the agreement and possibly obtain a refund or damages 
or both, or require us to incur additional expense in order to make the software solution or health care device meet these 
criteria or 2) subject us to claims or litigation by our clients or clinicians or directly by the patient. Additionally, such failures 
could damage our reputation and could negatively affect future sales. Our client agreements generally limit our liability arising 
from such claims but such limits may not be enforceable in certain jurisdictions or circumstances. Although we maintain 
liability insurance coverage, there can be no assurance that such coverage will cover any particular claim that has been 
brought or that may be brought in the future, that such coverage will prove to be adequate or that such coverage will continue 
to remain available on acceptable terms, if at all. A successful material claim or series of claims brought against us, if uninsured 
or under-insured, could materially harm our business, results of operations and financial condition. 

We may experience interruptions at our data centers or client support facilities.  Our business relies on the secure 
electronic transmission, data center storage and hosting of sensitive information, including protected health information, 
financial information and other sensitive information relating to our clients, company and workforce.  We perform data center 
and/or hosting services for certain clients, including the storage of critical patient and administrative data and support services 
through various client support facilities. If any of these systems are interrupted, damaged or breached by an unforeseen 
event or actions of a Cerner associate or contractor or a third party, including a cyber-attack, or fail for any extended period 
of time, it could have a material adverse impact on our results of operations.  Complete failure of all local public power and 
backup generators, impairment of all telecommunications lines, a concerted denial of service cyber-attack, a significant data 
breach, damage, injury or impairment (environmental, accidental, intentional or pandemic) to the buildings, the equipment 
inside the buildings housing our data centers, the personnel operating such facilities or the client data contained therein, or 
errors by the personnel trained to operate such facilities could cause a disruption in operations and negatively impact clients 
who depend on us for data center and system support services. We offer our clients disaster recovery services for additional 
fees to protect clients from isolated data center failures, leveraging our multiple data center facilities, however only a small 
percentage  of  our  hosted  clients  choose  to  contract  for  these  services. Additionally,  Cerner’s  core  systems  are  disaster 
tolerant as we have implemented redundancy across physically diverse data centers.  Any interruption in operations at our 
data centers and/or client support facilities could damage our reputation, cause us to lose existing clients, hurt our ability to 
obtain new clients, result in significant revenue loss, create potential liabilities for our clients and us and increase insurance 
and other operating costs. 

Our proprietary technology may be subject to claims for infringement or misappropriation of intellectual property 
rights of others, or may be infringed or misappropriated by others. We rely upon a combination of license agreements, 

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confidentiality policies and procedures, confidentiality provisions in employment agreements, confidentiality agreements with 
third parties and technical security measures to maintain the confidentiality, exclusivity and trade secrecy of our proprietary 
information. We also rely on trademark and copyright laws to protect our intellectual property rights in the United States and 
abroad. We continue to develop our patent portfolio of United States and global patents, but these patents do not provide 
comprehensive protection for the wide range of solutions, devices and services we offer. Despite our protective measures 
and  intellectual  property  rights,  we  may  not  be  able  to  adequately  protect  against  theft,  copying,  reverse-engineering, 
misappropriation, infringement or unauthorized use or disclosure of our intellectual property, which could have an adverse 
effect on our competitive position. 

In addition, we are routinely involved in intellectual property infringement or misappropriation claims and we expect this 
activity to continue or even increase as the number of competitors, patents and patent enforcement organizations in the 
HCIT market increases, the functionality of our software solutions and services expands, the use of open-source software 
increases and we enter new geographies and new markets such as health care device innovation, health care transactions, 
revenue cycle, population health management and life sciences. These claims, even if not meritorious, are expensive to 
defend and are often incapable of prompt resolution. If we become liable to third parties for infringing or misappropriating 
their intellectual property rights, we could be required to pay a substantial damage award, develop alternative technology, 
obtain a license or cease using, selling, offering for sale, licensing, importing, implementing or supporting the solutions, 
devices and services that violate the intellectual property rights. 

We may become subject to legal proceedings that could have a material adverse impact on our financial position 
and results of operations. From time to time and in the ordinary course of our business, we and certain of our subsidiaries 
may become involved in various legal proceedings. All such legal proceedings are inherently unpredictable and, regardless 
of the merits of the claims, litigation may be expensive, time-consuming and disruptive to our operations and distracting to 
management.  If resolved against us, such legal proceedings could result in excessive verdicts, injunctive relief or other 
equitable relief that may affect how we operate our business.  Similarly, if we settle such legal proceedings, it may affect how 
we operate our business. Future court decisions, alternative dispute resolution awards, business expansion or legislative 
activity  may  increase  our  exposure  to  litigation  and  regulatory  investigations.  In  some  cases,  substantial  non-economic 
remedies or punitive damages may be sought. Although we maintain liability insurance coverage, there can be no assurance 
that such coverage will cover any particular verdict, judgment or settlement that may be entered against us, that such coverage 
will prove to be adequate or that such coverage will continue to remain available on acceptable terms, if at all. If we incur 
liability that exceeds our insurance coverage or that is not within the scope of the coverage in legal proceedings brought 
against us, it could have an adverse effect on our business, financial condition and results of operations. 

We are subject to risks associated with our non-U.S. operations. We market, sell and service our solutions, devices and 
services globally. We have established offices around the world, including in the Americas, Europe, the Middle East and the 
Asia Pacific region. We plan to continue to expand our non-U.S. operations and enter new global markets. This expansion 
will require significant management attention and financial resources to develop successful direct and indirect non-U.S. sales 
and support channels. Our business is generally transacted in the local functional currency. In some countries, our success 
will depend in part on our ability to form relationships with local partners. There is a risk that we may sometimes choose the 
wrong partner. For these and other reasons, we may not be able to maintain or increase non-U.S. market demand for our 
solutions, devices and services. 

Non-U.S.  operations  are  subject  to  inherent  risks,  and  our  future  results  could  be  adversely  affected  by  a  variety  of 
uncontrollable and changing factors. These include, but are not limited to: 

•  Greater difficulty in collecting accounts receivable and longer collection periods 

•  Difficulties and costs of staffing and managing non-U.S. operations 

•  The impact of global economic conditions 

•  Effects of sovereign debt conditions, including budgetary constraints 

•  Unfavorable or volatile foreign currency exchange rates 

• 

Legal compliance costs or business risks associated with our global operations where: i) local laws and customs 
differ from those in the United States, or ii) risk is heightened with respect to laws prohibiting improper payments 
and bribery, including without limitation the U.S. Foreign Corrupt Practices Act, the U.K. Anti-Bribery Act and similar 
laws and regulations in foreign jurisdictions 

•  Certification, licensing or regulatory requirements 

•  Unexpected changes in regulatory requirements 

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•  Changes to or reduced protection of intellectual property rights in some countries 

•  Potentially adverse tax consequences and difficulties associated with repatriating cash generated or held abroad in 

a tax-efficient manner 

•  Different or additional functionality requirements or preferences 

•  Trade protection measures 

•  Export control regulations 

•  Health service provider or government spending patterns 

•  Natural disasters, war or terrorist acts 

• 

Labor disruptions that may occur in a country 

•  Poor selection of a partner in a country 

•  Political conditions which may impact sales or threaten the safety of associates or our continued presence in these 

countries 

Our failure to effectively hedge exposure to fluctuations in foreign currency exchange rates could unfavorably affect 
our performance. We currently utilize a non-derivative instrument to hedge our exposure to fluctuations in certain foreign 
currency exchange rates. This instrument may involve elements of market risk in excess of the amounts recognized in the 
Consolidated  Financial  Statements.  For  additional  information  about  market  risk  on  financial  instruments,  see  Item  7A 
“Quantitative and Qualitative Disclosures about Market Risk”. Further, our financial results from non-U.S. operations may be 
negatively affected if we fail to execute or if we improperly hedge our exposure to currency fluctuations.

We are subject to tax legislation in numerous countries; tax legislation initiatives or challenges to our tax positions 
could adversely affect our results of operations and financial condition. We are a global corporation with a presence 
in more than 25 countries. As such, we are subject to tax laws, regulations and policies of the United States federal, state 
and local governments and of other country jurisdictions. From time to time, various legislative initiatives may be proposed 
that could adversely affect our tax positions and/or our tax liabilities. There can be no assurance that our effective tax rate 
or tax payments will not be adversely affected by these initiatives. In addition, United States federal, state and local, as well 
as other countries’ tax laws and regulations are extremely complex and subject to varying interpretations. There can be no 
assurance that our tax positions will not be challenged by relevant tax authorities or that we would be successful in any such 
challenge, which could result in double taxation, penalties and interest payments. 

Our success depends upon the recruitment and retention of key personnel. To remain competitive in our industries, 
we must attract, motivate and retain highly skilled managerial, sales, marketing, consulting and technical personnel, including 
executives,  consultants,  programmers  and  systems  architects  skilled  in  the  HCIT,  health  care  devices,  health  care 
transactions, population health management, revenue cycle and life sciences industries and the technical environments in 
which our solutions, devices and services are needed. Competition for such personnel in our industries is intense in both 
the United States and abroad. Our failure to attract additional qualified personnel to meet our needs could have a material 
adverse effect on our prospects for long-term growth. In addition, we invest significant time and expense in training our 
associates, which increases their value to clients and competitors who may seek to recruit them and increases the cost of 
replacing them. Our success is dependent to a significant degree on the continued contributions of key management, sales, 
marketing, consulting and technical personnel. The unexpected loss of key personnel could have a material adverse impact 
on our business and results of operations, and could potentially inhibit development and delivery of our solutions, devices 
and services and market share advances. 

We depend on third party suppliers and our revenue and operating earnings could suffer if we fail to manage suppliers 
properly. We license or purchase intellectual property and technology (such as software, hardware and content) from third 
parties, including some competitors, and incorporate such third party software, hardware or content into or sell or license it 
in conjunction with our solutions, devices and services. We depend on some of the third party software, hardware or content 
in the operation and delivery of our solutions, devices and services. For instance, we currently depend on Microsoft and IBM 
technologies for portions of the operational capabilities of our Millennium solutions. Our remote hosting and cloud services 
businesses also rely on a limited number of suppliers for certain functions of these businesses, such as Oracle database 
technologies,  CITRIX  technologies  and  Cisco  networking  technologies. Additionally,  we  rely  on  EMC,  Hewlett  Packard, 
NetApp and IBM for our hardware technology platforms. 

Most of the third party software license contracts we have expire within one to five years, can be renewed only by mutual 
consent and may be terminated if we breach the terms of the license and fail to cure the breach within a specified period of 

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time. Most of these third party software licenses are non-exclusive; therefore, our competitors may obtain the right to use 
any of the technology covered by these licenses and use the technology to compete directly with us. 

If any of the third party suppliers were to change product offerings, cease actively supporting the technologies, fail to update 
and enhance the technologies to keep pace with changing industry standards, encounter technical difficulties in the continuing 
development of these technologies, significantly increase prices, terminate our licenses or supply contracts, suffer significant 
capacity or supply chain constraints or suffer significant disruptions, we would need to seek alternative suppliers and incur 
additional internal or external development costs to ensure continued performance of our solutions, devices and services. 
Such alternatives may not be available on attractive terms, or may not be as widely accepted or as effective as the intellectual 
property or technology provided by our existing suppliers. If the cost of licensing, purchasing or maintaining the third party 
intellectual property or technology significantly increases, our operating earnings could significantly decrease. In addition, 
interruption in functionality of our solutions, devices or services as a result of changes in third party suppliers could adversely 
affect our commitments to clients, future sales of solutions, devices and services, and negatively affect our revenue and 
operating earnings. 

We may be unable to successfully integrate the Siemens Health Services business with our business or to realize 
the  anticipated  benefits  of  the  acquisition  of  Siemens  Health  Services.    On  February  2,  2015,  we  completed  the 
acquisition of the assets of Siemens AG's health information technology business unit, Siemens Health Services.  The success 
of the acquisition of Siemens Health Services will depend, in part, on the ability to realize the anticipated synergies, growth 
opportunities and cost savings from integrating Siemens Health Services’ business with our business. The integration of two 
independent businesses is a complex, costly and time-consuming process and involves numerous risks, including difficulties 
in  the  assimilation  of  operations,  services,  solutions  and  personnel,  the  diversion  of  management’s  attention  from  other 
business concerns, the entry into markets in which we have little or no direct prior experience, the potential loss of Siemens 
Health  Services’  key  personnel,  and  the  potential  inability  to  maintain  the  goodwill  of  existing  clients. The  difficulties  of 
combining the operations of the companies include, among other factors:

•  managing a larger company;
• 

the  possibility  of  faulty  assumptions  underlying  expectations  regarding  the  integration  process,  including  the 
assumption of known and unknown liabilities;
integrating two business cultures;
creating  uniform  standards,  controls,  procedures,  policies  and  information  systems  and  minimizing  the  costs 
associated with such matters;
integrating  information  systems,  purchasing,  accounting,  finance,  legal,  sales,  billing,  payroll  and  regulatory 
compliance functions;
preserving  client,  supplier,  research  and  development,  distribution,  marketing,  promotion  and  other  important 
relationships;
commercializing solutions under development and increasing revenues from existing marketed solutions;
combining the sales force territories and competencies associated with the sale of solutions and services presently 
sold or provided by us or Siemens Health Services;
integrating personnel from different businesses while maintaining focus on providing consistent, high-quality solutions 
and client support and attracting prospective clients;
integrating complex technologies and solutions from different businesses in a manner that is seamless to clients; 
and
performance  shortfalls  as  a  result  of  the  diversion  of  management’s  attention  to  the  Siemens  Health  Services 
acquisition.

• 
• 

• 

• 

• 
• 

• 

• 

• 

If management is unable to successfully integrate the business of Siemens Health Services into our business in a manner 
that permits us to achieve the cost savings and operating synergies anticipated to result from the Siemens Health Services 
acquisition, such anticipated benefits of the Siemens Health Services acquisition may not be realized fully or at all or may 
take longer to realize than expected. Any significant diversion of management’s attention away from the ongoing businesses, 
and any difficulties encountered in the transition and integration process, could adversely affect our financial results. Moreover, 
the failure to achieve the anticipated benefits of the Siemens Health Services acquisition could result in increased costs or 
decreases in the amount of expected revenues.  Any of the above difficulties could adversely affect our ability to maintain 
relationships with clients, partners, suppliers and associates or our ability to achieve the anticipated benefits of the Siemens 
Health Services acquisition, or could reduce our earnings or otherwise adversely affect our business and financial results.

We intend to continue strategic business acquisitions and other combinations, which are subject to inherent risks. 
In order to expand our solutions, device offerings and services and grow our market and client base, we may continue to 

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seek and complete strategic business acquisitions and other combinations that we believe are complementary to our business. 
Acquisitions have inherent risks which may have a material adverse effect on our business, financial condition, operating 
results or prospects, including, but not limited to: 1) failure to successfully integrate the business and financial operations, 
services, intellectual property, solutions or personnel of an acquired business and to maintain uniform standard controls, 
policies and procedures; 2) diversion of management’s attention from other business concerns; 3) entry into markets in which 
we have little or no direct prior experience; 4) failure to achieve projected synergies and performance targets; 5) loss of 
clients  or  key  personnel;  6)  incurrence  of  debt  or  assumption  of  known  and  unknown  liabilities;  7)  write-off  of  software 
development costs, goodwill, client lists and amortization of expenses related to intangible assets; 8) dilutive issuances of 
equity securities; and, 9) accounting deficiencies that could arise in connection with, or as a result of, the acquisition of an 
acquired company, including issues related to internal control over financial reporting and the time and cost associated with 
remedying  such  deficiencies.  If  we  fail  to  successfully  integrate  acquired  businesses  or  fail  to  implement  our  business 
strategies with respect to these acquisitions, we may not be able to achieve projected results or support the amount of 
consideration paid for such acquired businesses. 

We could suffer losses due to asset impairment charges. We assess our goodwill for impairment during the second 
quarter every year and on an interim date should events or changes in circumstances indicate the carrying value of goodwill 
may not be recoverable in accordance with provisions of Accounting Standards Codification Topic 350, Intangibles – Goodwill 
and Other. Declines in business performance or other factors could cause the fair value of a reporting unit to be revised 
downward and could result in a non-cash impairment charge. This could negatively affect our reported net earnings. 

Volatility and disruption resulting from global economic conditions could negatively affect our business, results of 
operations and financial condition. Although certain indices and economic data have shown signs of stabilization in the 
United  States  and  certain  global  markets,  there  can  be  no  assurance  that  these  improvements  will  be  broad-based  or 
sustainable, nor is it clear how, if at all, they will affect the markets relevant to us. As a result, our operating results may be 
impacted  by  the  health  of  the  global  economy.  Volatility  and  disruption  in  global  capital  and  credit  markets  may  lead  to 
slowdowns or declines in client spending which could adversely affect our business and financial performance. Our business 
and financial performance, including new business bookings and collection of our accounts receivable, may be adversely 
affected by current and future economic conditions (including a reduction in the availability of credit, higher energy costs, 
rising interest rates, financial market volatility and lower than expected economic growth) that cause a slowdown or decline 
in client spending. Reduced purchases by our clients or changes in payment terms could adversely affect our revenue growth 
and cause a decrease in our cash flow from operations. Bankruptcies or similar events affecting clients may cause us to 
incur bad debt expense at levels higher than historically experienced. Further, volatility and disruption in global financial 
markets may also limit our ability to access the capital markets at a time when we would like, or need, to raise capital, which 
could have an impact on our ability to react to changing economic and business conditions. Accordingly, if global financial 
and economic volatility continues or worsens, our business, results of operations and financial condition could be materially 
and adversely affected. 

If we are unable to manage our growth in the new markets in which we offer solutions, health care devices or services, 
our business and financial results could suffer.  Our future financial results will depend in part on our ability to profitably 
manage our business in the new markets that we enter.  Over the past several years, we have engaged in the identification 
of, and competition for, growth and expansion opportunities in the areas of analytics, revenue cycle and population health.  
In order to achieve those initiatives, we will need to, among other things, recruit, train, retain and effectively manage associates, 
manage changing business conditions and implement and improve our technical, administrative, financial control and reporting 
systems for offerings in those areas.  Difficulties in managing future growth in new markets could have a significant negative 
impact on our business, financial condition and results of operations.

We will incur significant additional expenses in connection with the integration of the Siemens Health Services 
business into Cerner.  As we work to integrate the business, we expect to incur significant additional expenses relating to 
the integration of personnel, geographically diverse operations, information technology systems, accounting systems, clients, 
and strategic partners of each business and the implementation of consistent standards, policies, and procedures, and we 
may be subject to material write downs in assets and charges to earnings, which are expected to include severance pay and 
other costs. The integration process will be long-term and will continue to create significant expenses.

We have restrictive covenants in our debt agreements, which may restrict our flexibility to operate our business.  If 
we do not comply with these restrictive covenants, our failure could result in material and adverse effects on our 
operating results and our financial condition.  Our debt agreements contain customary restrictive covenants, including 
limitations  on  consolidated  indebtedness,  liens,  investments,  subsidiary  investments,  asset  dispositions,  and  restricted 
payments, and require us to maintain certain leverage and interest coverage ratios. Failure to comply with these covenants 

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could result in an event of default that, if not cured or waived, could result in reduced liquidity for the Company and could 
have a material adverse effect on our operating results and financial condition.

Risks Related to the Health Care Information Technology, Health Care Device, Health Care Transaction and Population 
Health Management Industry 

The health care industry is subject to changing political, economic and regulatory influences. For example, the Health 
Insurance Portability and Accountability Act of 1996 (as modified by The Health Information Technology for Economic and 
Clinical  Health Act  (HITECH)  provisions  of  the American  Recovery  and  Reinvestment Act  of  2009)  (collectively,  HIPAA) 
continues to have a direct impact on the health care industry by requiring national provider identifiers and standardized 
transactions/code sets, operating rules and necessary security and privacy measures in order to ensure the appropriate level 
of privacy of protected health information. These regulatory factors affect the purchasing practices and operation of health 
care organizations. 

Many health care providers are consolidating to create integrated health care delivery systems with greater market power. 
These providers may try to use their market power to negotiate price reductions for our solutions, health care devices and 
services. As the health care industry consolidates, our client base could be eroded, competition for clients could become 
more intense and the importance of landing new client relationships becomes greater. 

The Patient Protection and Affordable Care Act, which was amended by the Health Care and Education Reconciliation Act 
of 2010, became law in 2010. This comprehensive health care reform legislation included provisions to control health care 
costs, improve health care quality, and expand access to affordable health insurance. Together with ongoing statutory and 
budgetary policy developments at a federal level, this health care reform legislation could include changes in Medicare and 
Medicaid payment policies and other health care delivery administrative reforms that could potentially negatively impact our 
business and the business of our clients. Because not all the administrative rules implementing health care reform under the 
legislation have  been finalized, and because of ongoing federal fiscal budgetary pressures yet to be resolved for federal 
health programs, the full impact of the health care reform legislation and of further statutory actions to reform healthcare 
payment on our business is unknown, but there can be no assurances that health care reform legislation will not adversely 
impact either our operational results or the manner in which we operate our business. Health care industry participants may 
respond by reducing their investments or postponing investment decisions, including investments in our devices, solutions 
and services. 

The health care industry is highly regulated, and thus, we are subject to a number of laws, regulations and industry 
initiatives,  non-compliance  with  certain  of  which  could  materially  adversely  affect  our  operations  or  otherwise 
adversely affect our business, financial condition and operating results. As a participant in the health care industry, 
our operations and relationships, and those of our clients, are regulated by a number of local, state, federal and foreign 
governmental entities.  The impact of these regulations on us is direct, to the extent that we are ourselves subject to these 
laws and regulations, and is also indirect because, in a number of situations, even though we may not be directly regulated 
by specific health care laws and regulations, our solutions, devices and services must be capable of being used by our clients 
in a way that complies with those laws and regulations. There is a significant and wide-ranging number of regulations both 
within the United States and abroad, such as regulations in the areas of health care fraud, e-prescribing, claims processing 
and transmission, health care devices, the security and privacy of patient data and interoperability standards, that may be 
directly or indirectly applicable to our operations and relationships or the business practices of our clients.  Specific risks 
include, but are not limited to, the following: 

Health Care Fraud. Federal and state governments continue to enhance regulation of and increase their scrutiny over practices 
involving health care fraud, waste and abuse affecting health care providers whose services are reimbursed by Medicare, 
Medicaid and other government health care programs. Our health care provider clients, as well as our provision of products 
and services to government entities subject our business to laws and regulations on fraud and abuse which, among other 
things,  prohibit  the  direct  or  indirect  payment  or  receipt  of  any  remuneration  for  patient  referrals,  or  arranging  for  or 
recommending referrals or other business paid for in whole or in part by these federal or state health care programs. Federal 
enforcement personnel have substantial funding, powers and remedies to pursue suspected or perceived fraud and abuse. 
The effect of this government regulation on our clients is difficult to predict. Many of the regulations applicable to our clients 
and that may be applicable to us, including those relating to marketing incentives offered in connection with health care 
device sales, are vague or indefinite and have not been interpreted by the courts. They may be interpreted or applied by a 
prosecutorial, regulatory or judicial authority in a manner that could broaden their applicability to us or require our clients to 
make changes in their operations or the way in which they deal with us. If such laws and regulations are determined to be 
applicable to us and if we fail to comply with any applicable laws and regulations, we could be subject to civil and criminal 

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penalties, sanctions or other liability, including exclusion from government health programs, which could have a material 
adverse effect on our business, results of operations and financial condition.  Even an unsuccessful challenge by a regulatory 
or prosecutorial authority of our activities could result in adverse publicity, could require a costly response from us and could 
adversely affect our business, financial condition and results of operations. 

Preparation, Transmission and Submission of Medical Claims for Reimbursement.  Our solutions are capable of electronically 
transmitting claims for services and items rendered by a physician to many patients' payers for approval and reimbursement.  
We also provide services to our clients that include the coding, preparation and submission of claims for medical service to 
payers for reimbursement.  Such claims are governed by federal and state laws.  Federal law provides civil liability to any 
person that knowingly submits a claim to a payer, including Medicare, Medicaid and private health plans, seeking payment 
for any services or items that have not been provided to the patient.  Federal law may also impose criminal penalties for 
intentionally submitting such false claims.  We have policies and procedures in place that we believe result in the accurate 
and complete preparation, transmission, submission and collection of claims, provided that the information given to us by 
our clients is also accurate and complete.  The HIPAA security, privacy and transaction standards, as discussed below, also 
have a potentially significant effect on our claims preparation, transmission and submission services, since those services 
must be structured and provided in a way that supports our clients' HIPAA compliance obligations. In connection with these 
laws, we may be subjected to federal or state government investigations and possible penalties may be imposed upon us; 
false claims actions may have to be defended; private payers may file claims against us; and we may be excluded from 
Medicare, Medicaid or other government-funded health care programs.  Any investigation or proceeding related to these 
laws, even if unwarranted or without merit, may have a material adverse effect on our business, results of operations and 
financial condition.

Implementation of ICD-10 Coding for Medical Coding.  The Centers for Medicare & Medicaid Services (CMS) has mandated 
that all providers, payers, clearinghouses and billing services implement the use of new patient codes for medical coding, 
referred to as ICD-10 codes on or before October 1, 2015.  This mandate substantially increases the number of medical 
billing codes by which providers will seek reimbursement, increasing the complexity of submitting claims for reimbursement.  
Claims submitted after October 1, 2015 must use ICD-10 codes or they will not be paid. Our efforts to provide services and 
solutions that enable our clients to comply with the ICD-10 mandate could be time consuming and expensive. In addition, 
due to the effort and expense of complying with the ICD-10 mandate, our clients may postpone or cancel decisions to purchase 
our solutions and services.  Either of the foregoing could have a material adverse effect on our business, financial condition 
and results of operations.

Regulation of Health Care Devices. The United States Food and Drug Administration (the FDA) has determined that certain 
of our solutions are health care devices that are actively regulated under the Federal Food, Drug and Cosmetic Act (Act) and 
amendments to the Act. Other countries have similar regulations in place related to health care devices, that now or may in 
the future apply to certain of our solutions. If other of our solutions are deemed to be actively regulated health care devices 
by the FDA or similar regulatory agencies in countries where we do business, we could be subject to extensive requirements 
governing pre- and post-marketing activities including pre-market notification clearance. Complying with these health care 
device regulations on a global perspective is time consuming and expensive and could be subject to unanticipated and 
significant delays. Further, it is possible that these regulatory agencies may become more active in regulating software and 
health care devices that are used in health care. If we are unable to obtain the required regulatory approvals for any such 
solutions or health care devices, our short and long term business plans for these solutions or health care devices could be 
delayed or canceled. 

There have been eight FDA inspections at various Cerner sites since 2003. Inspections conducted at our World Headquarters 
and Innovations Campus in 2010 resulted in the issuance of an FDA Form 483 observation to which we responded promptly. 
The FDA has taken no further action with respect to the Form 483 observation that was issued in 2010. The remaining FDA 
inspections, including inspections at our world headquarters in 2006, 2007 and 2014, resulted in no issuance of a Form 483. 
We remain subject to periodic FDA inspections and we could be required to undertake additional actions to comply with the 
Act and any other applicable regulatory requirements. Our failure to comply with the Act and any other applicable regulatory 
requirements could have a material adverse effect on our ability to continue to manufacture, distribute and deliver our solutions, 
services and devices. The FDA has many enforcement tools including recalls, product corrections, seizures, injunctions, 
refusal to grant pre-market clearance of products, civil fines and criminal prosecutions. Any of the foregoing could have a 
material adverse effect on our business, results of operations and financial condition. 

Security and Privacy of Patient Information. Federal, state, local and foreign laws regulate the confidentiality of patient records 
and the circumstances under which those records may be used and released. These regulations govern both the disclosure 
and use of confidential patient medical record information and require the users of such information to implement specified 

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security and privacy measures. United States regulations currently in place governing electronic health data transmissions 
continue to evolve and are often unclear and difficult to apply. Laws in non-U.S. jurisdictions may have similar or even stricter 
requirements related to the treatment of patient information. 

In the United States, HIPAA regulations require national standards for some types of electronic health information transactions 
and the data elements used in those transactions to ensure the integrity, security and confidentiality of health information 
and  standards  to  protect  the  privacy  of  individually  identifiable  health  information.  Covered  entities  under  HIPAA,  which 
include  health  care  organizations  such  as  our  clients,  our  employer  clinic  business  model  and  our  claims  processing, 
transmission and submission services, are required to comply with the privacy standards, the transaction regulations and 
the security regulations. Moreover, the HITECH provisions of ARRA, and associated regulatory requirements, extend many 
of the HIPAA obligations, formerly imposed only upon covered entities, to business associates as well. As a business associate 
of our clients who are covered entities, we were in most instances already contractually required to ensure compliance with 
the HIPAA regulations as they pertain to handling of covered client data. However, the extension of these HIPAA obligations 
to business associates by law has created additional liability risks related to the privacy and security of individually identifiable 
health information. 

Evolving HIPAA and HITECH-related laws or regulations in the U.S. and data privacy and security laws or regulations in non-
U.S. jurisdictions could restrict the ability of our clients to obtain, use or disseminate patient information. This could adversely 
affect demand for our solutions if they are not re-designed in a timely manner in order to meet the requirements of any new 
interpretations or regulations that seek to protect the privacy and security of patient data or enable our clients to execute 
new  or  modified  health  care  transactions.  We  may  need  to  expend  additional  capital,  software  development  and  other 
resources to modify our solutions and devices to address these evolving data security and privacy issues.  Furthermore, our 
failure to maintain confidentiality of sensitive personal information in accordance with the applicable regulatory requirements 
could damage our reputation and expose us to claims, fines and penalties. 

In Europe, we are subject to the European Union (“EU”) data protection regulations, including the EU Directive on Data 
Protection, which requires member states to impose minimum restrictions on the collection and use of personal data that, in 
some respects, are more stringent, and impose more significant burdens on subject businesses, than current privacy standards 
in the United States. The EU regulations establish several obligations that organizations must follow with respect to use of 
personal data, including a prohibition on the transfer of personal information from the EU to other countries whose laws do 
not protect personal data to an adequate level of privacy or security. In addition to this EU-wide legislation, certain member 
states have adopted more stringent data protection standards. Cerner has addressed these requirements by certification to 
the US - EU and US - Switzerland Safe Harbor Frameworks.  The costs of compliance with, and other burdens imposed by, 
such laws, regulations and policies, or modifications thereto, that are applicable to us may limit the use and adoption of our 
solutions and could have a material adverse impact on our results of operations.

Applicable statutes and regulations have granted broad enforcement powers to regulatory agencies to investigate and enforce 
our compliance with these privacy and security laws and regulations.  Governmental enforcement personnel have substantial 
funding, powers and remedies to pursue suspected or perceived violations.  If we fail to comply with any applicable laws or 
regulations, we could be subject to civil penalties, sanctions or other liability.  Enforcement investigations, even if meritless, 
could have a negative impact on our reputation, cause us to lose existing clients or limit our ability to attract new clients.

Interoperability Standards. Our clients are concerned with and often require that our software solutions and health care 
devices be interoperable with other third party HCIT suppliers. Market forces or governmental/regulatory authorities could 
create  software  interoperability  standards  that  would  apply  to  our  solutions,  health  care  devices  or  solutions,  and  if  our 
software solutions, health care devices or services are not consistent with those standards, we could be forced to incur 
substantial additional development costs to conform. The Office of the National Coordinator for Health Information Technology 
(ONC) has developed a comprehensive set of criteria for the functionality, interoperability and security of various software 
modules  in  the  HCIT  industry.  ONC,  however,  continues  to  modify  and  refine  those  standards. Achieving  certification  is 
becoming a competitive requirement, resulting in increased software development and administrative expense to conform 
to these requirements. 

ARRA Meaningful Use Program. Various federal, state and non-U.S. government agencies are also developing standards 
that could become mandatory for systems purchased by these agencies. For example, ARRA requires “meaningful use of 
certified electronic health record technology” by health care providers in order to receive stimulus funds from the U.S. federal 
government.  Regulations  have  been  issued  that  identify  standards  and  implementation  specifications  and  establish  the 
certification standards for qualifying electronic health record technology. Nevertheless, these standards and specifications 
are subject to interpretation by the entities designated to certify such technology. While a combination of our solutions have 

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been certified as meeting the initial standards for certified health record technology, the regulatory standards to achieve 
certification will continue to evolve over time. We may incur increased development costs and delays in delivering solutions 
if we need to upgrade our software, devices or health care devices to be in compliance with these varying and evolving 
standards.  In  addition,  delays  in  interpreting  these  standards  may  result  in  postponement  or  cancellation  of  our  clients’ 
decisions to purchase our solutions or health care devices. If our software solutions, devices or health care devices are not 
compliant  with  these  evolving  standards,  our  market  position  and  sales  could  be  impaired  and  we  may  have  to  invest 
significantly in changes to our software solutions, devices or health care devices. 

We operate in intensely competitive and dynamic industries, and our ability to successfully compete and continue 
to grow our business depends on our ability to respond quickly to market changes and changing technologies and 
to bring competitive new solutions, devices, features and services to market in a timely fashion. The market for health 
care information systems, health care solutions and services to the health care industry is intensely competitive, dynamically 
evolving and subject to rapid technological and innovative changes. Development of new proprietary technology or services 
is complex, entails significant time and expense and may not be successful. We cannot guarantee that we will be able to 
introduce new solutions, devices or services on schedule, or at all, nor can we guarantee that such solutions, devices or 
services will achieve market acceptance.  Moreover, we cannot guarantee that errors will not be found in our new solution 
releases, devices or services before or after commercial release, which could result in solution, device or service delivery 
redevelopment  costs,  harm  to  our  reputation,  lost  sales,  license  terminations  or  renegotiations,  product  liability  claims, 
diversion of resources to remedy errors and loss of, or delay in, market acceptance. 

Certain of our competitors have greater financial, technical, product development, marketing or other resources than us and 
some of our competitors offer software solutions, devices or services that we do not offer. Our principal existing competitors 
are set forth above under Part I, Item 1 "Competition". 

In addition, we expect that major software information systems companies, large information technology consulting service 
providers and system integrators, start-up companies and others specializing in the health care industry may offer competitive 
software solutions, devices or services. As we continue to develop new health care devices and services to address areas 
such as analytics, transaction services, HCIT and device integration, revenue cycle and population health management, we 
expect to face new competitors, and these competitors may have more experience in these markets and/or more established 
relationships with prospective clients.  We face strong competition and often face downward price pressure, which could 
adversely affect our results of operations or liquidity. Additionally, the pace of change in the health care information systems 
market  is  rapid  and  there  are  frequent  new  software  solution  introductions,  software  solution  enhancements,  device 
introductions,  device  enhancements  and  evolving  industry  standards  and  requirements.  There  are  a  limited  number  of 
hospitals and other health care providers in the United States market and in recent years, the health care industry has been 
subject  to  increasing  consolidation.  If  we  are  unable  to  recognize  the  impact  of  industry  consolidation,  falling  costs  and 
technological advancements in a timely manner, or we are too inflexible to rapidly adjust our business models, our growth 
ambitions and financial results could be negatively affected materially. 

Risks Related to Our Common Stock 

Our quarterly operating results may vary, which could adversely affect our stock price. Our quarterly operating results 
have  varied  in  the  past  and  may  continue  to  vary  in  future  periods,  including  variations  from  guidance,  expectations  or 
historical results or trends. Quarterly operating results may vary for a number of reasons including demand for our solutions, 
devices and services, the financial condition of our current and potential clients, our long sales cycle, potentially long installation 
and implementation cycles for larger, more complex systems, accounting policy changes and other factors described in this 
section and elsewhere in this report. As a result of health care industry trends and the market for our solutions, a large 
percentage of our revenues are generated by the sale and installation of larger, more complex and higher-priced systems. 
The sales process for these systems is lengthy and involves a significant technical evaluation and commitment of capital 
and other resources by the client. Sales may be subject to delays due to changes in clients’ internal budgets, procedures for 
approving large capital expenditures, competing needs for other capital expenditures, additions or amendments to federal, 
state or local regulations, availability of personnel resources or by actions taken by competitors. Delays in the expected sale, 
installation or implementation of these large systems may have a significant negative impact on our anticipated quarterly 
revenues and consequently our earnings, since a significant percentage of our expenses are relatively fixed. 

Revenue recognized in any quarter may depend upon our or our clients’ abilities to meet project milestones. Delays in meeting 
these milestone conditions or modification of the project plan could result in a shift of revenue recognition from one quarter 
to another and could have a material adverse effect on results of operations for a particular quarter.

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Our revenues from system sales historically have been lower in the first quarter of the year and greater in the fourth quarter 
of the year, primarily as a result of clients’ year-end efforts to make final capital expenditures for the then-current year.

Our sales forecasts may vary from actual sales in a particular quarter. We use a “pipeline” system, a common industry 
practice, to forecast sales and trends in our business. Our sales associates monitor the status of all sales opportunities, such 
as the date when they estimate that a client will make a purchase decision and the potential dollar amount of the sale. These 
estimates are aggregated periodically to generate a sales pipeline. We compare this pipeline at various points in time to 
evaluate trends in our business. This analysis provides guidance in business planning and forecasting, but these pipeline 
estimates are by their nature speculative. Our pipeline estimates are not necessarily reliable predictors of revenues in a 
particular quarter or over a longer period of time, partially because of changes in the pipeline and in conversion rates of the 
pipeline into contracts that can be very difficult to estimate. A negative variation in the expected conversion rate or timing of 
the pipeline into contracts, or in the pipeline itself, could cause our plan or forecast to be inaccurate and thereby adversely 
affect business results. For example, a slowdown in information technology spending, adverse economic conditions, new 
federal, state or local regulations related to our industry or a variety of other factors can cause purchasing decisions to be 
delayed, reduced in amount or cancelled, which would reduce the overall pipeline conversion rate in a particular period of 
time. Because a substantial portion of our contracts are completed in the latter part of a quarter, we may not be able to adjust 
our cost structure quickly enough in response to a revenue shortfall resulting from a decrease in our pipeline conversion rate 
in any given fiscal quarter. 

The trading price of our common stock may be volatile. The market for our common stock may experience significant 
price and volume fluctuations in response to a number of factors including actual or anticipated variations in operating results, 
articles or rumors about our performance or solutions, devices or services, announcements of technological innovations or 
new services or products by our competitors or us, changes in expectations of future financial performance or estimates of 
securities analysts, governmental regulatory action, health care reform measures, client relationship developments, economic 
conditions and changes occurring in the securities markets in general and other factors, many of which are beyond our 
control. For instance, our quarterly operating results have varied in the past and may continue to vary in future periods, due 
to a number of reasons including, but not limited to, demand for our solutions, devices and services, the financial condition 
of our current and potential clients, our long sales cycle, potentially long installation and implementation cycles for larger, 
more complex and higher-priced systems, accounting policy changes and other factors described herein. As a matter of 
policy, we do not generally comment on our stock price or rumors. 

Furthermore, the stock market in general, and the markets for software, health care devices, other health care solutions and 
services and information technology companies in particular, have experienced extreme volatility that often has been unrelated 
to the operating performance of particular companies. These broad market and industry fluctuations may adversely affect 
the trading price of our common stock, regardless of actual operating performance. 

Our Directors have authority to issue preferred stock and our corporate governance documents contain anti-takeover 
provisions. Our Board of Directors has the authority to issue up to 1,000,000 shares of preferred stock and to determine 
the preferences, rights and privileges of those shares without any further vote or action by the shareholders. The rights of 
the holders of common stock may be harmed by rights granted to the holders of any preferred stock that may be issued in 
the future. 

In addition, some provisions of our Certificate of Incorporation and Bylaws could make it more difficult for a potential acquirer 
to acquire a majority of our outstanding voting stock. These include provisions that provide for a classified board of directors, 
prohibit shareholders from taking action by written consent and restrict the ability of shareholders to call special meetings. 
We are also subject to provisions of Delaware law that prohibit us from engaging in any business combination with any 
interested shareholder for a period of three years from the date the person became an interested shareholder, unless certain 
conditions are met, which could have the effect of delaying or preventing a change of control.

Factors that May Affect Future Results of Operations, Financial Condition or Business 

Statements made in this report, the Annual Report to Shareholders of which this report is made a part, other reports and 
proxy statements filed with the Securities and Exchange Commission (SEC), communications to shareholders, press releases 
and oral statements made by representatives of the Company that are not historical in nature, or that state the Company’s 
or management’s intentions, hopes, beliefs, expectations, plans, goals or predictions of future events or performance, may 
constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and 
Section 21E of the Securities Exchange Act of 1934, as amended (the Exchange Act). Forward-looking statements can often 
be identified by the use of forward-looking terminology, such as “could,” “should,” “will,” “intended,” “continue,” “believe,” 

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“may,”  “expect,”  “hope,”  “anticipate,”  “goal,”  “forecast,”  “plan,”  “guidance”  or  “estimate”  or  the  negative  of  these  words, 
variations thereof or similar expressions. Forward-looking statements are not guarantees of future performance or results. 
They involve risks, uncertainties and assumptions. It is important to note that any such performance and actual results, 
financial condition or business, could differ materially from those expressed in such forward-looking statements. Factors that 
could cause or contribute to such differences include, but are not limited to, those discussed in this Item 1A. Risk Factors 
and elsewhere herein or in other reports filed with the SEC. Other unforeseen factors not identified herein could also have 
such an effect. We undertake no obligation to update or revise forward-looking statements to reflect changed assumptions, 
the occurrence of unanticipated events or changes in future operating results, financial condition or business over time. 

Item 1B. Unresolved Staff Comments

None

Item 2. Properties

Our properties consist mainly of owned and leased office and data center facilities. 

Our United States corporate world headquarters is located in a Company-owned office park (the Headquarters Campus) in 
North Kansas City, Missouri.  The Headquarters Campus and three other nearby locations, collectively contain approximately 
2.22 million gross square feet of useable space situated on 278 acres of land.  The Headquarters Campus and the nearby 
properties primarily house office space, but also include space for other business needs, such as our Healthe Clinic and our 
Headquarters Campus data centers. 

Company-owned  office  space,  known  as  the  Innovation  Campus,  houses  associates  from  our  intellectual  property 
organization and consists of 790,000 gross square feet of useable space located in Kansas City, Missouri.

Owned office space known as the Continuous Campus, houses associates who manage and support our clients' IT systems 
and consists of 611,000 gross square feet of useable space located in Kansas City, Kansas.  Construction of the Continuous 
Campus was completed in February 2014.

Our Cerner-operated data center facilities, which are used to provide remote hosting, disaster recovery and other services 
to our clients, are located at the Headquarters Campus and a leased facility in Lee’s Summit, Missouri. 

We have purchased approximately 260 acres of land located in Kansas City, Missouri. This property, known as the Trails 
Campus,  was  acquired  as  a  site  for  future  office  space  development  to  further  accommodate  our  anticipated  growth.  
Construction on the Trails Campus began in November 2014.

As  of  the  end  of  2014,  we  leased  additional  office  space  in Tempe, Arizona;  Carlsbad,  Culver  City  and  Garden  Grove, 
California; Denver, Colorado; Lenexa, Kansas; Waltham, Massachusetts; Minneapolis and Rochester, Minnesota; Columbia, 
Nevada, Lee’s Summit and Kansas City, Missouri; Durham, North Carolina; New Concord, Ohio; Franklin, Tennessee; Salt 
Lake City, Utah; Burlington, Vermont; and Vienna, Virginia. Globally, we also leased office space in: Brisbane, Sydney and 
Melbourne, Australia; Sao Paulo, Brazil; Peterborough and Toronto, Ontario, Canada; Cairo, Egypt; London, England; Paris, 
France;  Idstein,  Germany;  Bangalore,  India;  Dublin,  Ireland;  Kuala  Lumpur,  Malaysia;  Riyadh,  Saudi Arabia;  Singapore; 
Madrid, Spain; Doha, Qatar; and Abu Dhabi and Dubai, United Arab Emirates.

In connection with our acquisition of Siemens Health Services on February 2, 2015, we acquired approximately 110 acres 
of  property  in  Malvern,  Pennsylvania.   This  property  includes  approximately  675,000  square  feet  of  office  space,  and  a 
102,000 square foot data center. We also now lease additional office space in various locations, globally.

Item 3. Legal Proceedings

We are not a party to and none of our property is subject to any material pending legal proceedings, other than ordinary 
routine litigation incidental to our business.

Item 4. Mine Safety Disclosures

Not applicable

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Part II

Item 5. Market for the Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity 
Securities 

Our common stock trades on The NASDAQ Global Select MarketSM under the symbol CERN. The following table sets forth 
the high, low and last sales prices for the fiscal quarters of 2014 and 2013 as reported by The Nasdaq Stock Market®. 

First Quarter
Second Quarter
Third Quarter
Fourth Quarter

High

2014

Low

Last

High

2013(a)

Low

$

$

63.07
56.94
60.07
66.45

$

51.65
48.39
50.30
55.75

56.15
51.27
58.66
65.03

$

$

47.37
49.68
52.61
58.24

$

38.76
45.60
46.06
52.55

Last

47.37
48.05
52.61
55.58

(a) Sales prices have been retroactively adjusted to give effect to the 2-for-1 stock split effective June 28, 2013.

At February 6, 2015, there were approximately 940 owners of record. To date, we have paid no cash dividends and we do 
not intend to pay cash dividends in the foreseeable future. We believe it is in the shareholders’ best interest for us to reinvest 
funds in the operation of the business. 

The following table provides information with respect to Common Stock purchases by the Company during the fourth fiscal 
quarter of 2014: 

(In millions, except share data)

Period
September 28, 2014 - October 25, 2014
October 26, 2014 - November 22, 2014
November 23, 2014 - January 3, 2015

Total

Total Number of
Shares
Purchased (a)

Average Price
Paid per Share

—
658
—
658

$

$

—
63.34
—
63.34

Total Number of
Shares Purchased
as Part of Publicly
Announced Plans
or Programs (b)

Approximate Dollar
Value of Shares
That May Yet Be
Purchased Under
the Plans or
Programs (b)

— $
—
—
—

100.0
100.0
100.0

(a)   All of the shares of common stock, par value $0.01 per share, presented on the table above were originally granted to employees as restricted 
stock pursuant to our 2011 Omnibus Equity Incentive Plan (the Omnibus Plan). The Omnibus Plan allows for the withholding of shares to satisfy 
minimum tax obligations due upon the vesting of restricted stock.  Pursuant to the Omnibus Plan, the shares reflected above were relinquished 
by employees in exchange for our agreement to pay federal and state withholding obligations resulting from the vesting of the Company’s restricted 
stock.

(b) 

In May 2014, our Board of Directors approved an amendment to the stock repurchase program that was authorized in December 2013.  Under 
the amendment, the Company may repurchase shares of our common stock up to an aggregate of $317.0 million, excluding transaction costs. 
During 2014, the Company repurchased 4.1 million shares for consideration of $217.0 million, excluding transaction costs, pursuant to a Rule 
10b5-1 plan.  As of January 3, 2015, $100.0 million remains available under the authorized program.

See Part III, Item 12 for information relating to securities authorized for issuance under our equity compensation plans. 

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Item 6. Selected Financial Data

(In thousands, except per share data)

Statement of Operations Data:

Revenues
Operating earnings
Earnings before income taxes
Net earnings

Earnings per share:

Basic
Diluted

Weighted average shares outstanding:

Basic
Diluted

Balance Sheet Data:

2014
(1)(2)

2013
(1)(3)

2012
(1)

2011
(1)

2010
(1)

$ 3,402,703
763,084
774,174
525,433

$ 2,910,748
576,012
588,054
398,354

$ 2,665,436
571,662
587,708
397,232

$ 2,203,153
459,798
469,694
306,627

$ 1,850,222
359,333
362,212
237,272

1.54
1.50

1.16
1.13

1.16
1.13

0.91
0.88

0.72
0.69

342,150
350,386

343,636
352,281

341,861
351,394

337,267
347,734

329,833
341,695

Working capital
Total assets
Long-term debt and capital lease obligations, excl. current
installments
Shareholders' equity

$ 1,714,471
4,530,565

$ 1,121,276
4,098,364

$ 1,210,394
3,704,468

$ 1,063,593
3,000,358

$

840,129
2,422,790

62,868
3,565,968

111,717
3,167,664

136,557
2,833,650

86,821
2,310,681

67,923
1,905,297

(1) 

Includes share-based compensation expense. The impact of this expense is as follows:

(In thousands, except share data)

2014

2013

2012

2011

2010

Total share-based compensation expense

Amount of related income tax benefit

Net impact on earnings

Decrease to diluted earnings per share

$

$

$

62,965

(22,101)

40,864

0.12

$

$

$

48,954

(18,607)

30,347

0.09

$

$

$

38,112

(14,578)

23,534

0.07

$

$

$

29,479

(11,256)

18,223

0.05

$

$

$

24,903

(9,329)

15,574

0.05

(2) 

Includes $15.8 million of pre-tax costs in connection with our acquisition of Siemens Health Services, as further described in Note 2 of the notes 
to consolidated financial statements.

(3) 

Includes a pre-tax settlement charge of $106.2 million, as further described in Note 11 of the notes to consolidated financial statements.

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Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations

The  following  Management  Discussion  and Analysis  (MD&A)  is  intended  to  help  the  reader  understand  our  results  of 
operations and financial condition. This MD&A is provided as a supplement to, and should be read in conjunction with, our 
financial statements and the accompanying notes to the financial statements (Notes). 

Our fiscal year ends on the Saturday closest to December 31. Fiscal year 2014 consisted of 53 weeks and ended on January 3, 
2015, and fiscal years 2013 and 2012 each consisted of 52 weeks and ended on December 28, 2013 and December 29, 
2012, respectively.  The additional week in fiscal 2014 impacts the results of operations discussion below, for the comparison 
of fiscal years 2014 and 2013.  All references to years in this MD&A represent fiscal years unless otherwise noted.

Management Overview

Our revenues are primarily derived by selling, implementing and supporting software solutions, clinical content, hardware, 
devices and services that give health care providers secure access to clinical, administrative and financial data in real time, 
allowing them to improve quality, safety and efficiency in the delivery of health care.

Our fundamental strategic focus is the creation of organic growth by investing in research and development (R&D) to create 
solutions and services for the health care industry. This strategy has driven strong growth over the long-term, as reflected 
in five- and ten-year compound annual revenue growth rates of 14% or more. This growth has also created an important 
strategic footprint in health care, with Cerner® solutions in more than 18,000 facilities worldwide, including hospitals, physician 
practices, laboratories, ambulatory centers, behavioral health centers, cardiac facilities, radiology clinics, surgery centers, 
extended care facilities, retail pharmacies, and employer sites. Selling additional solutions back into this client base is an 
important element of our future revenue growth. We are also focused on driving growth through market share expansion by 
strategically aligning with health care providers that have not yet selected a supplier and by displacing competitors in health 
care settings that are looking to replace their current supplier. 

We expect to drive growth through solutions and services that reflect our ongoing ability to innovate and expand our reach 
into health care. Examples of these include our CareAware® health care device architecture and devices, Cerner ITWorks 
services, revenue cycle solutions and services, and population health solutions and services. Finally, we believe there is 
significant opportunity for growth outside of the United States, with many non-U.S. markets focused on health care information 
technology as part of their strategy to improve the quality and lower the cost of health care. 

Beyond our strategy for driving revenue growth, we are also focused on earnings growth. Similar to our history of growing 
revenue, our net earnings have increased at compound annual rates of 20% or more over the most recent five- and ten-year 
periods.  We expect to drive continued earnings growth through ongoing revenue growth coupled with margin expansion, 
which we expect to achieve through efficiencies in our implementation and operational processes and by leveraging R&D 
investments and controlling general and administrative expenses. 

We are also focused on continuing to deliver strong levels of cash flow, which we expect to do by continuing to grow earnings 
and prudently managing capital expenditures. 

Results Overview 

The Company delivered strong levels of bookings, revenues, earnings and operating cash flows in 2014. 

New business bookings revenue in 2014, which reflects the value of executed contracts for software, hardware, professional 
services and managed services, was $4.3 billion, which is an increase of 13% compared to $3.8 billion in 2013.  Our 2014 
revenues increased 17% to $3.4 billion compared to $2.9 billion in 2013. The year-over-year increase in revenue reflects 
ongoing demand for Cerner's core solutions and services driven by our clients’ needs to keep up with regulatory requirements, 
increased contributions from Cerner ITWorks and Cerner revenue cycle solutions and services, and attaining new clients. 

Our 2014 net earnings were $525.4 million compared to $398.4 million in 2013. Diluted earnings per share were $1.50 in 
2014 compared to $1.13 in 2013. The 2014 and 2013 net earnings and diluted earnings per share reflect the impact of stock-
based compensation expense. The effect of these expenses reduced the 2014 net earnings and diluted earnings per share 
by $40.9 million and $0.12, respectively, and the 2013 net earnings and diluted earnings per share by $30.3 million and 
$0.09, respectively. The 2014 net earnings and diluted earnings per share also reflect the impact of acquisition costs related 
to our acquisition of Siemens Health Services, as further described below.  These costs reduced net earnings and diluted 

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earnings per share by $10.1 million and $0.03, respectively.  The 2013 net earnings and diluted earnings per share also 
reflect the impact of a settlement charge, as further described in Note (11) of our notes to consolidated financial statements.  
The effect of this charge reduced 2013 net earnings and diluted earnings per share by $68.1 million and $0.19, respectively. 

We had cash collections of receivables of $3.5 billion in 2014 compared to $3.1 billion in 2013. Days sales outstanding was 
66 days for the 2014 fourth quarter compared to 67 days for both the 2014 third quarter and the 2013 fourth quarter.  Operating 
cash flows for 2014 were strong at $847.0 million compared to $695.9 million in 2013.

Siemens Health Services

On February 2, 2015, we acquired substantially all of the assets, and assumed certain liabilities of Siemens Health Services, 
the health information technology business unit of Siemens AG, a stock corporation established under the laws of Germany.  
Siemens Health Services offers a portfolio of enterprise-level clinical and financial health care information technology solutions, 
as well as departmental, connectivity, population health, and care coordination solutions globally.  Solutions are offered on 
the Soarian, Invision, and i.s.h.med platforms, among others.  Siemens Health Services also offers a range of complementary 
and support services including hosting and managed services, implementation services, and strategic consulting.

We believe the acquisition enhances our organic growth opportunities as it provides us a larger base into which we can sell 
our  combined  portfolio  of  solutions  and  services.  The  acquisition  also  augments  our  non-U.S.  footprint  and  growth 
opportunities, increases our ability and scale for R&D investment, and adds approximately 5,500 highly-skilled associates 
that  will  enhance  our  capabilities.    These  factors,  combined  with  the  synergies  and  economies  of  scale  expected  from 
combining the operations of Cerner and Siemens Health Services, are the basis for the acquisition.

Consideration for the acquisition was $1.37 billion of cash, consisting of the $1.3 billion agreed upon price plus working 
capital  adjustments.   The  purchase  price  is  subject  to  certain  post-closing  adjustments  for  working  capital  and  pension 
obligations, as specified in the Master Sale and Purchase Agreement dated August 5, 2014, as amended.

The operating results of Siemens Health Services will be combined with our operating results subsequent to the purchase 
date of February 2, 2015.  We expect the acquisition of Siemens Health Services to have a significant impact on our results 
of  operations  in  2015.   As  a  reference  for  magnitude,  we  expect  the  Siemens  Health  Services  business  to  contribute 
approximately $1.0 billion of revenues in 2015.  We are currently unable to provide estimates of contributions to GAAP net 
earnings and diluted earnings per share, primarily due to the timing of the transaction in proximity to the date of this filing.  
The initial accounting for the acquisition, including the preliminary allocation of purchase price, is incomplete as of the filing 
date.  

Health Care Information Technology Market Outlook 

We have provided an assessment of the health care information technology market under “Health Care and Health Care IT 
Industry” in Part I, Item 1 "Business." 

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Results of Operations

Fiscal Year 2014 Compared to Fiscal Year 2013

(In thousands)
Revenues

System sales
Support and maintenance
Services
Reimbursed travel

Total revenues

Costs of revenue

Costs of revenue

Total margin

Operating expenses

Sales and client service
Software development
General and administrative

Total operating expenses

Total costs and expenses

Operating earnings

Other income, net
Income taxes

Net earnings

Revenues & Backlog

2014

% of
Revenue

2013

% of
Revenue

%
Change  

$

945,858
724,840
1,642,119
89,886

28% $
21%
48%
3%

847,809
661,979
1,330,851
70,109

29%
23%
46%
2%

3,402,703

100%

2,910,748

100%

604,377

2,798,326

1,395,568
392,805
246,869

2,035,242

2,639,619

763,084

11,090
(248,741)

18%

82%

41%
12%
7%

60%

78%

22%

514,722

2,396,026

1,173,051
338,786
308,177

1,820,014

2,334,736

576,012

12,042
(189,700)

18%

82%

40%
12%
11%

63%

80%

20%

12 %
9 %
23 %
28 %

17 %

17 %

17 %

19 %
16 %
(20)%

12 %

13 %

32 %

$

525,433

$

398,354

32 %

Revenues increased 17% to $3.4 billion in 2014, as compared to $2.9 billion in 2013.

•  System sales, which include revenues from the sale of licensed software (including perpetual license sales and 
software as a service), technology resale  (hardware, devices, and sublicensed  software), deployment  period 
licensed software upgrade rights, installation fees, transaction processing and subscriptions, increased 12% to 
$945.9 million in 2014 from $847.8 million in 2013. The increase in system sales was primarily driven by strong 
growth in software and subscriptions of $65.4 million and $22.9 million, respectively.

•  Support and maintenance revenues increased 9% to $724.8 million in 2014 compared to $662.0 million in 2013. 
This increase was attributable to continued success at selling Cerner Millennium applications and implementing 
them at client sites. We expect that support and maintenance revenues will continue to grow as the base of 
installed Cerner Millennium systems grows.

•  Services revenue, which includes professional services, excluding installation, and managed services, increased 
23% to $1.6 billion in 2014 from $1.3 billion in 2013. This increase was driven by growth in CernerWorks managed 
services of $70.0 million as a result of continued demand for our hosting services and a $241.3 million increase 
in professional services due to increased implementation and consulting activities.

Revenue backlog, which reflects contracted revenue that has not yet been recognized as revenue, increased 19% to 
$10.6 billion in 2014 compared to $8.9 billion in 2013.  This increase was driven by growth in new business bookings 
during the past four quarters, including continued strong levels of managed services, Cerner ITWorks and Cerner revenue 
cycle services bookings that typically have longer contract terms. 

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Costs of Revenue

Cost of revenues as a percentage of total revenues was 18% in both 2014 and 2013. 

Cost of revenues includes the cost of reimbursed travel expense, sales commissions, third party consulting services and 
subscription content and computer hardware, devices and sublicensed software purchased from manufacturers for delivery 
to  clients.  It  also  includes  the  cost  of  hardware  maintenance  and  sublicensed  software  support  subcontracted  to  the 
manufacturers. Such costs, as a percent of revenues, typically have varied as the mix of revenue (software, hardware, 
devices, maintenance, support, services and reimbursed travel) carrying different margin rates changes from period to 
period. Cost of revenues does not include the costs of our client service personnel who are responsible for delivering our 
service offerings. Such costs are included in sales and client service expense.

Operating Expenses

Total operating expenses increased 12% to $2.0 billion in 2014, compared with $1.8 billion in 2013.

•  Sales and client service expenses as a percent of total revenues were 41% in 2014, compared to 40% in 2013. 
These expenses increased 19% to $1.4 billion in 2014, from $1.2 billion in 2013.  Sales and client service expenses 
include salaries of sales, marketing, support, and services personnel, depreciation and other expenses associated 
with our CernerWorks managed service business, communications expenses, unreimbursed travel expenses, 
expense for share-based payments, and trade show and advertising costs. The increase as a percent of revenue 
reflects a higher mix of services during the period that was driven by strong services revenue growth.

•  Software development expenses as a percent of revenue were 12% in 2014 and 2013.  Expenditures for software 
development  reflect  ongoing  development  and  enhancement  of  the  Cerner  Millennium  and  HealtheIntent 
platforms, with a focus on supporting key initiatives to enhance physician experience, revenue cycle and population 
health solutions.  A summary of our total software development expense in 2014 and 2013 is as follows:

(In thousands)

Software development costs
Capitalized software costs
Capitalized costs related to share-based payments
Amortization of capitalized software costs

Total software development expense

For the Years Ended

2014

2013

$ 467,158
(175,262)
(2,538)
103,447

$ 418,747
(172,211)
(2,438)
94,688

$ 392,805

$ 338,786

•  General and administrative expenses as a percent of total revenues were 7% in 2014, compared to 11% in 2013. 
These expenses decreased 20% to $246.9 million in 2014, from $308.2 million in 2013. General and administrative 
expenses include salaries for corporate, financial and administrative staffs, utilities, communications expenses, 
professional fees, depreciation and amortization, transaction gains or losses on foreign currency, expense for 
share-based payments and acquisition costs. The 2013 amount includes a $106.2 million settlement charge, as 
further described in Note (11) of our notes to consolidated financial statements.  The decrease of $61.3 million 
was primarily driven by the 2013 settlement charge, offset by $15.8 million of acquisition costs related to the 
acquisition of Siemens Health Services and a $14.8 million increase in corporate personnel costs, as we have 
continued to increase such personnel to support our overall revenue growth.

Non-Operating Items

•  Other income was $11.1 million in 2014 and $12.0 million in 2013.  Refer to Note (12) of the notes to consolidated 

financial statements for further detail on the composition of other income.

•  Our effective tax rate was 32% in both 2014 and 2013.  The rate includes net favorable permanent differences 
recognized  in  both  periods.  Refer  to  Note  (13) of  the  notes  to  consolidated  financial  statements  for  further 
information regarding our effective tax rate.

In January 2013, the research and development tax credit was extended retroactively from January 1, 2012 to 
December 31, 2013.  In the first quarter of 2013, we recognized the research and development tax credit related 
to 2012 as a favorable discrete item and the credit related to 2013 as a component of the overall 2013 effective 
tax rate.  The credit expired on December 31, 2013, but in the fourth quarter of 2014, was retroactively reinstated 

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from January 1, 2014 to December 31, 2014.  We recognized the research and development tax credit related 
to 2014 in the fourth quarter of 2014.  We estimate the expiration of the research and development tax credit on 
December 31, 2014 will negatively impact our effective tax rate for 2015 by approximately one percentage point, 
unless such credit is reinstated.

Operations by Segment

We have two operating segments:  Domestic and Global. The Domestic segment  includes  revenue  contributions and 
expenditures associated with business activity in the United States. The Global segment includes revenue contributions 
and expenditures linked to business activity in Aruba, Australia, Austria, Brazil, Canada, Cayman Islands, Chile, Egypt, 
England, Finland, France, Germany, Guam, India, Ireland, Israel, Malaysia, Mexico, Netherlands, Qatar, Saudi Arabia, 
Singapore, Spain, Switzerland and the United Arab Emirates.

The following table presents a summary of our operating segment information for the years ended 2014 and 2013:

(In thousands)

Domestic Segment
Revenues
Costs of revenue
Operating expenses
Total costs and expenses

Domestic operating earnings

Global Segment
Revenues
Costs of revenue
Operating expenses
Total costs and expenses

Global operating earnings

Other, net

Consolidated operating earnings

Domestic Segment

2014

% of
Revenue

2013

% of
Revenue

%
Change  

$ 3,021,790
542,210
677,817
1,220,027

100%
18%
22%
40%

$ 2,550,115
458,540
600,341
1,058,881

100%
18%
24%
42%

1,801,763

60%

1,491,234

58%

380,913
62,167
131,096
193,263

100%
16%
34%
51%

360,633
56,182
115,281
171,463

100%
16%
32%
48%

187,650

49%

189,170

52%

(1,226,329)

(1,104,392)

$

763,084

$

576,012

18%
18%
13%
15%

21%

6%
11%
14%
13%

(1)%

11%

32%

•  Revenues increased 18% to $3.0 billion in 2014 from $2.6 billion in 2013. This increase was driven by strong 

growth across most of our business.

•  Cost of revenues was 18% of revenues in both 2014 and 2013.

•  Operating expenses increased 13% to $677.8 million in 2014 from $600.3 million in 2013, due primarily to growth 

in professional services expenses.

Global Segment

•  Revenues increased 6% to $380.9 million in 2014 from $360.6 million in 2013. This increase was primarily driven 
by  increases  in  managed  services  and  professional  services  of  $11.3  million  and  $12.7  million,  respectively, 
partially offset by a decline in software revenues of $7.3 million.

•  Cost of revenues was 16% of revenues in both 2014 and 2013. 

•  Operating expenses increased 14% to $131.1 million in 2014 from $115.3 million in 2013, due primarily to an 

increase in bad debt expense.

Other, net

Operating results not attributed to an operating segment include expenses, such as centralized professional services 
costs,  software  development,  marketing,  general  and  administrative,  stock-based  compensation,  acquisition  costs, 

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depreciation and amortization.  These expenses increased 11% to $1.2 billion in 2014 from $1.1 billion in 2013.  The 
increase was driven by an increase in corporate personnel costs of $182.7 million, as we have continued to increase such 
personnel to support our overall revenue growth, combined with $15.8 million of acquisition costs related to our acquisition 
of Siemens Health Services.  This is partially offset by the 2013 settlement charge of $106.2 million, as further described 
in Note (11) of our notes to consolidated financial statements. 

Fiscal Year 2013 Compared to Fiscal Year 2012 

(In thousands)
Revenues

System sales
Support and maintenance
Services
Reimbursed travel

Total revenues

Costs of revenue

Costs of revenue

Total margin

Operating expenses

Sales and client service
Software development
General and administrative

Total operating expenses

Total costs and expenses

Operating earnings

Other income, net
Income taxes

Net earnings

Revenues & Backlog

2013

% of
Revenue

2012

% of
Revenue

%
Change  

$

847,809
661,979
1,330,851
70,109

29% $
23%
46%
2%

902,799
604,247
1,103,082
55,308

34%
23%
41%
2%

2,910,748

100%

2,665,436

100%

514,722

2,396,026

1,173,051
338,786
308,177

1,820,014

2,334,736

576,012

12,042
(189,700)

18%

82%

40%
12%
11%

63%

80%

20%

608,197

2,057,239

1,020,640
301,370
163,567

1,485,577

2,093,774

571,662

16,046
(190,476)

23%

77%

38%
11%
6%

56%

79%

21%

(6)%
10 %
21 %
27 %

9 %

(15)%

16 %

15 %
12 %
88 %

23 %

12 %

1 %

$

398,354

$

397,232

— %

Revenues increased 9% to $2.9 billion in 2013, as compared to $2.7 billion in 2012.

•  System sales decreased 6% to $847.8 million in 2013 from $902.8 million in 2012. The decrease in system sales 
was driven by lower levels of technology resale, which more than offset growth in licensed software, subscriptions, 
and software as a service.

•  Support and maintenance revenues increased 10% to $662.0 million in 2013 compared to $604.2 million in 2012. 
This increase was attributable to continued success at selling Cerner Millennium systems and implementing them 
at client sites. 

•  Services revenue increased 21% to $1.3 billion in 2013 compared to $1.1 billion in 2012. This increase was driven 
by growth in CernerWorks managed services as a result of continued demand for our hosting services and an 
increase in professional services due to increased implementation and consulting activities and growth in Cerner 
ITWorks and Cerner RevWorks services.

Revenue backlog increased 23% to $8.9 billion in 2013 compared to $7.3 billion in 2012 This increase was driven by 
growth in new business bookings during the past four quarters, including continued strong levels of managed services, 
Cerner ITWorks and Cerner revenue cycle services bookings that typically have longer contract terms. 

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Costs of Revenue

Cost of revenues as a percentage of total revenues was 18% of total revenues in 2013, as compared to 23% of total 
revenues in 2012. The lower cost of revenues as a percent of revenue was driven by a lower mix of technology resale, 
which carries a higher cost of revenue.

Operating Expenses

Total operating expenses increased 23% in 2013 to $1.8 billion as compared to $1.5 billion in 2012.

•  Sales and client service expenses as a percent of total revenues were 40% in 2013, as compared to 38% in 2012. 
These expenses increased 15% to $1.2 billion in 2013, from $1.0 billion in 2012. The increase as a percent of 
revenue reflects a higher mix of services during 2013 that was driven by strong services revenue growth and the 
decline in technology resale revenue. 

•  Software development expenses as a percent of revenue were 12% in 2013, as compared to 11% in 2012.  These 
expenses increased 12% in 2013 to $338.8 million, from $301.4 million in 2012.  The increase in both expensed 
and capitalized software development expenditures reflects a focus on development and enhancement of solutions 
that support key initiatives to enhance physician experience, revenue cycle, and population health.  A summary 
of our total software development expense in 2013 and 2012 is as follows:

(In thousands)

Software development costs
Capitalized software costs
Capitalized costs related to share-based payments
Amortization of capitalized software costs

Total software development expense

For the Years Ended

2013

2012

$ 418,747
(172,211)
(2,438)
94,688

$ 319,828
(98,067)
(2,122)
81,731

$ 338,786

$ 301,370

•  General and administrative expenses as a percent of total revenues were 11% in 2013, compared to 6% in 2012. 
These expenses increased 88% to $308.2 million in 2013 from $163.6 million in 2012.  The 2013 amount includes 
a  $106.2  million  settlement  charge,  as  further  described  in  Note  (11)  of  our  notes  to  consolidated  financial 
statements.  Absent this charge, the increase in general and administrative expenses was primarily driven by an 
increase in corporate personnel costs, as we have continued to increase such personnel to support our overall 
revenue growth, and an increase in amortization expense due to acquired intangibles.

Non-Operating Items

• 

Interest income decreased to $15.3 million in 2013 from $16.5 million in 2012 due primarily to a slight decrease 
in investment returns. Interest expense decreased to $4.2 million in 2013 from $5.1 million in 2012 due primarily 
to  payments  on  our  long-term  debt,  offset  by  increased  capital  lease  obligations.  Other  income  in  2012  also 
includes a $4.5 million gain recognized on the disposition of one of our cost-method investments.

•  Our effective tax rate was 32% in both 2013 and 2012.  The rate includes net favorable permanent differences 
recognized  in  both  periods.  Refer  to  Note  (13) of  the  notes  to  consolidated  financial  statements  for  further 
information regarding our effective tax rate.

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Operations by Segment

The following table presents a summary of our operating segment information for the years ended 2013 and 2012:

(In thousands)

Domestic Segment
Revenues
Costs of revenue
Operating expenses
Total costs and expenses

Domestic operating earnings

Global Segment
Revenues
Costs of revenue
Operating expenses
Total costs and expenses

Global operating earnings

Other, net

Consolidated operating earnings

Domestic Segment

2013

% of
Revenue

2012

% of
Revenue

%
Change  

$ 2,550,115
458,540
600,341
1,058,881

100%
18%
24%
42%

$ 2,341,304
548,813
506,249
1,055,062

100%
23%
22%
45%

1,491,234

58%

1,286,242

55%

360,633
56,182
115,281
171,463

100%
16%
32%
48%

324,132
59,384
131,580
190,964

100%
18%
41%
59%

189,170

52%

133,168

41%

(1,104,392)

(847,748)

$

576,012

$

571,662

9%
(16)%
19%
—%

16%

11%
(5)%
(12)%
(10)%

42%

30%

1%

•  Revenues increased 9% to $2.6 billion in 2013 from $2.3 billion in the same period in 2012. This increase was 
primarily driven by strong growth across most of our business, partially offset by lower levels of technology resale.

•  Cost of revenues was 18% of revenues in 2013, compared to 23% in 2012. The lower cost of revenues as a 
percent of revenue was primarily driven by a lower mix of technology resale, which carries a higher cost of revenue.

•  Operating expenses increased 19% to $600.3 million in 2013, from $506.2 million in 2012, due primarily to growth 

in managed services and professional services expenses.

Global Segment

•  Revenues increased 11% to $360.6 million in 2013 from $324.1 million in 2012. This increase was primarily driven 

by growth across most of our business, partially offset by lower levels of technology resale.

•  Cost of revenues was 16% in 2013, compared to 18% in 2012.  The lower cost of revenues as a percent of 

revenue was primarily driven by a lower mix of technology resale, which carries a higher cost of revenue.

•  Operating expenses decreased 12% to $115.3 million in 2013 from $131.6 million in 2012, due primarily to a 

decrease in non-personnel and bad debt expense.

Other, net

These expenses increased 30% to $1.1 billion in 2013 from $847.7 million in 2012. The 2013 amount includes a $106.2 
million settlement charge, as further described in Note (11) of our notes to consolidated financial statements.  Absent this 
charge, the increase was primarily due to growth in corporate and development personnel costs, along with increased 
depreciation and amortization related to acquired intangibles.  This was partially offset by increased software capitalization.

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Liquidity and Capital Resources

Our liquidity is influenced by many factors, including the amount and timing of our revenues, our cash collections from our 
clients and the amount we invest in software development, acquisitions and capital expenditures.

Our principal sources of liquidity are our cash, cash equivalents, which primarily consist of money market funds, commercial 
paper, and time deposits with original maturities of less than 90 days, and short-term investments. At the end of 2014, we 
had cash and cash equivalents of $635.2 million and short-term investments of $785.7 million, as compared to cash and 
cash equivalents of $202.4 million and short-term investments of $677.0 million at the end of 2013.  

The non-U.S. subsidiaries for which we have elected to indefinitely reinvest earnings outside the U.S. held approximately 
11% of our aggregate cash, cash equivalents and short-term investments at January 3, 2015.  As part of our current business 
strategy, we plan to indefinitely reinvest the earnings of these foreign operations; however, should the earnings of these 
foreign operations be repatriated, we would accrue and pay tax on such earnings, which may be material.

In January 2015, we issued $500.0 million aggregate principal amount of Senior Notes.  Proceeds from the Senior Notes 
are available for general corporate purposes.  Refer to Note (9) of the notes to consolidated financial statements for additional 
information regarding the Senior Notes.

We maintain a $100.0 million multi-year revolving credit facility, which expires in February 2017. The facility provides an 
unsecured revolving line of credit for working capital purposes, along with a letter of credit facility. As of the end of 2014, we 
had no outstanding borrowings under this agreement; however, we had $16.6 million of outstanding letters of credit, which 
reduced our available borrowing capacity to $83.4 million.  Refer to Note (9) of the notes to consolidated financial statements 
for additional information regarding our credit facility.

On February 2, 2015 we acquired Siemens Health Services, as discussed above.  Consideration for the acquisition was 
$1.37 billion of cash, consisting of the $1.3 billion agreed upon price plus working capital adjustments.  We used a combination 
of cash on hand and proceeds from the sale of investments to fund the acquisition.

We believe that our present cash position, together with cash generated from operations, short-term investments and, if 
necessary, our available line of credit, will be sufficient to meet anticipated cash requirements during 2015.

The following table summarizes our cash flows in 2014, 2013 and 2012:

(In thousands)

Cash flows from operating activities
Cash flows from investing activities
Cash flows from financing activities
Effect of exchange rate changes on cash

Total change in cash and cash equivalents

Cash and cash equivalents at beginning of period

Cash and cash equivalents at end of period

Free cash flow (non-GAAP)

For the Years Ended
2013

2012

2014

$ 847,027
(284,567)
(120,324)
(9,310)
432,826

$ 695,865
(688,429)
(119,389)
(2,790)
(114,743)

$ 708,314
(701,631)
66,034
1,257
73,974

202,377

317,120

243,146

$ 635,203

$ 202,377

$ 317,120

$ 392,643

$ 168,339

$ 424,696

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Cash from Operating Activities

(In thousands)

Cash collections from clients
Cash paid to employees and suppliers and other
Cash paid for interest
Cash paid for taxes, net of refund

Total cash from operations

For the Years Ended
2013

2012

2014

$ 3,480,591
(2,483,559)
(5,682)
(144,323)

$ 3,050,633
(2,172,418)
(6,973)
(175,377)

$ 2,714,315
(1,840,682)
(6,448)
(158,871)

$ 847,027

$ 695,865

$ 708,314

Cash flow from operations increased $151.2 million in 2014 compared to 2013, due primarily to 2013 including a payment 
related to the previously mentioned settlement charge, along with an increase in 2014 of cash impacting earnings.  Cash 
flow from operations decreased $12.4 million in 2013 compared to 2012, due primarily to the aforementioned settlement 
charge.  During 2014, 2013 and 2012, we received total client cash collections of $3.5 billion, $3.1 billion and $2.7 billion, 
respectively, of which 2%, 2% and 3%, respectively, were received from third party client financing arrangements and non-
recourse payment assignments.  Days sales outstanding was 66 days in the fourth quarter of 2014, compared to 67 days 
for both the 2014 third quarter and the 2013 fourth quarter.  Revenues provided under support and maintenance agreements 
represent recurring cash flows.  Support and maintenance revenues increased 9% in 2014 and 10% in 2013.  We expect 
these revenues to continue to grow as the base of installed Cerner Millennium systems grows.

Cash from Investing Activities

(In thousands)

Capital purchases
Capitalized software development costs
Purchases of investments, net of sales and maturities
Acquisition of businesses, net of cash acquired
Other, net

Total cash flows from investing activities

For the Years Ended
2013

2012

2014

$ (276,584) $ (352,877) $ (183,429)
(100,189)
(354,603)
(40,540)
(22,870)

(177,800)
190,810
(7,476)
(13,517)

(174,649)
(36,221)
(67,877)
(56,805)

$ (284,567) $ (688,429) $ (701,631)

Cash flows from investing activities consist primarily of capital spending, short-term investment, and acquisition activities. 

Our  capital  spending  in  2014  has  been  driven  by  capitalized  equipment  purchases  primarily  to  support  growth  in  our 
CernerWorks managed services business, investments in a cloud infrastructure to support cloud-based solutions, building 
and improvement purchases to support our facilities requirements and capitalized spending to support our ongoing software 
development initiatives.  Capital spending is expected to increase in 2015, as we continue our current capital and software 
development initiatives, fund equipment purchases necessary in connection with our acquisition of Siemens Health Services, 
and construction on our Trails Campus.

Short-term investment activity historically consists of the investment of cash generated by our business in excess of what is 
necessary to fund operations. The 2014 activity is impacted by a change in investment mix, whereas we have invested more 
heavily in cash equivalents versus short-term and long-term investments, as we prepared to fund our acquisition of Siemens 
Health Services.  Refer to Notes (2) and (3) of the notes to consolidated financial statements.  We expect short-term investment 
activity to moderate in 2015 as excess cash will primarily be used to fund capital spending and acquisition activity. 

During 2014, we acquired 100% of the outstanding membership interests of InterMedHx, LLC for $7.5 million.  In 2013, we 
acquired the net assets of Kaufman & Keen, LLC (doing business as PureWellness) and 100% of the outstanding stock of 
Labotix Corporation for $67.5 million, net of cash acquired.  During 2012, we completed our acquisition of Anasazi Software, 
Inc. for $40.5 million, net of cash acquired.  We expect to continue seeking and completing strategic business acquisitions 
that are complementary to our business.

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Cash from Financing Activities 

(In thousands)

Repayment of long-term debt and capital lease obligations
Cash from option exercises (including excess tax benefits)
Treasury stock purchases
Contingent consideration payments for acquisition of businesses
Cash grants
Other, net

Total cash flows from financing activities

For the Years Ended
2013

2012

2014

$

(14,930) $
71,411
(217,082)
(10,617)
48,000
2,894

(24,700) $
71,330
(170,042)
(800)
—
4,823

(17,083)
86,517
—
(3,400)
—
—

$ (120,324) $ (119,389) $

66,034

Cash inflows from stock option exercises are dependent on a number of factors, including the price of our common stock, 
grant activity under our stock option and equity plans, and overall market volatility.  We expect cash inflows from stock option 
exercises to continue in 2015 based on the number of exercisable options at the end of 2014 and our current stock price.

In  May  2014,  our  Board  of  Directors  approved  an  amendment  to  the  stock  repurchase  program  that  was  authorized  in 
December 2013.  Under the amendment, the Company may repurchase shares of our common stock up to an aggregate of 
$317.0 million, excluding transaction costs.  In 2014, we purchased 4.1 million shares for total consideration of $217.1 million.  
At the end of 2014, $100.0 million remains available for purchases under the program.  We may continue to purchase shares 
under this program in 2015, which will be dependent on a number of factors, including the price of our common stock. 

In December 2012, our Board of Directors authorized a stock repurchase program of up to $170.0 million, excluding transaction 
costs, of our common stock.  During 2013, we repurchased 3.6 million shares for total consideration of $170.0 million. This 
program is now complete.

In September 2014 we paid $10.6 million of the contingent consideration related to our acquisition of PureWellness.  We 
expect additional contingent consideration payments in 2015 related to our acquisitions of PureWellness and InterMedHx. 
Refer  to  Note  (2)  of  the  notes  to  consolidated  financial  statements  for  additional  information  regarding  our  contingent 
consideration arrangements.

In January 2014 we received $48.0 million of cash grants from the Kansas Department of Commerce for project costs in 
connection  with  the  construction  of  our  Continuous  Campus.    Refer  to  Note  (17)  of  the  notes  to  consolidated  financial 
statements for additional information.

Free Cash Flow 

(In thousands)

Cash flows from operating activities (GAAP)
Capital purchases
Capitalized software development costs

Free cash flow (non-GAAP)

For the Years Ended
2013

2012

2014

$ 847,027
(276,584)
(177,800)

$ 695,865
(352,877)
(174,649)

$ 708,314
(183,429)
(100,189)

$ 392,643

$ 168,339

$ 424,696

Free cash flow increased $224.3 million from 2013 to 2014.  This increase is largely due to an increase in cash flows from 
operations combined with a decrease in capital purchases, primarily due to the completion of construction on our Continuous 
Campus.  Free cash flow for 2013 also includes a payment related to the settlement charge, described in Note (11) of our 
notes to consolidated financial statements.  Free cash flow decreased $256.4 million from 2012 to 2013.  This decrease was 
primarily due to the previously mentioned settlement charge, combined with increased capital spending in 2013 to support 
our growth initiatives and facilities requirements and capitalized spending to support our ongoing software development 
initiatives.  We believe our free cash flow levels reflect continued strength in our earnings.  Free cash flow is a non-GAAP 
financial measure used by management along with GAAP results to analyze our earnings quality and overall cash generation 
of the business. The presentation of free cash flow is not meant to be considered in isolation, nor as a substitute for, or 
superior to, GAAP results and investors should be aware that non-GAAP measures have inherent limitations and should be 
read only in conjunction with our consolidated financial statements prepared in accordance with GAAP.  Free cash flow may 
also be different from similar non-GAAP financial measures used by other companies and may not be comparable to similarly 

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titled captions of other companies due to potential inconsistencies in the method of calculation. We believe free cash flow is 
important  to  enable  investors  to  better  understand  and  evaluate  our  ongoing  operating  results  and  allows  for  greater 
transparency in the review of our overall financial, operational and economic performance, because free cash flow takes into 
account the capital expenditures necessary to operate our business.

Contractual Obligations, Commitments and Off Balance Sheet Arrangements 

The following table represents a summary of our contractual obligations and commercial commitments at the end of 2014, 
except short-term purchase order commitments arising in the ordinary course of business. 

(In thousands)

Balance sheet obligations(a):

Long-term debt obligations (b)
Interest on long-term debt obligations

Capital lease obligations

Interest on capital lease obligations

Other obligations:

Operating lease obligations

Purchase obligations

2015

2016

2017

2018

2019

2020 and
thereafter

Total

Payments Due by Period

$

14,233

$

789

53,227

2,741

23,525

42,300

— $

—

— $

—

34,510

1,458

21,693

23,481

19,522

530

21,467

6,762

— $

— $

— $

14,233

—

6,721

156

—

2,115

22

—

—

—

789

116,095

4,907

19,294

4,345

14,984

4,001

39,607

8,000

140,570

88,889

Total

$ 136,815

$

81,142

$

48,281

$

30,516

$

21,122

$

47,607

$ 365,483

(a)    At the end of 2014, liabilities for unrecognized tax benefits were $7.2 million. 
(b)    Amounts do not include the long-term debt issued in January 2015.

We have no off balance sheet arrangements as defined in Regulation S-K. The effects of inflation on our business during 
2014, 2013 and 2012 were not significant.

Recent Accounting Pronouncements

Refer  to  Note  (1)  of  the  notes  to  consolidated  financial  statements  for  information  regarding  recently  issued  accounting 
pronouncements. 

Critical Accounting Policies

We believe that there are several accounting policies that are critical to understanding our historical and future performance, 
as these policies affect the reported amount of revenue and other significant areas involving our judgments and estimates. 
These significant accounting policies relate to revenue recognition, software development, potential impairments of goodwill, 
and income taxes. These policies and our procedures related to these policies are described in detail below and under specific 
areas  within  this  MD&A.  In  addition,  Note  (1)  to  the  consolidated  financial  statements  expands  upon  discussion  of  our 
accounting policies. 

Revenue Recognition
We recognize revenue within our multiple element arrangements, including software and software-related services, using 
the residual method. Key factors in our revenue recognition model are our assessments that installation services are essential 
to the functionality of our software, whereas implementation services are not, and the length of time it takes for us to achieve 
the  delivery  and  installation  milestones  for  our  licensed  software.  If  our  business  model  were  to  change  such  that 
implementation services are deemed to be essential to the functionality of our software, the period of time over which our 
licensed software revenue would be recognized would lengthen. 

We generally recognize revenue from the sale of our licensed software over two key milestones, delivery and installation, 
based on percentages that reflect the underlying effort from planning to installation. Generally, both milestones are achieved 
in the quarter the contracts are executed. If the period of time to achieve our delivery and installation milestones for our 

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licensed software were to lengthen, our milestones would be adjusted and the timing of revenue recognition for our licensed 
software could materially change.

We also recognize revenue for certain projects in which services are deemed essential to the functionality of the software 
using the percentage of completion method. Our revenue recognition is dependent upon our ability to reliably estimate the 
direct labor hours to complete a project which generally can span several years. We utilize our historical project experience 
and detailed planning process as a basis for our future estimates to complete current projects. Significant delays in completion 
of the projects, unforeseen cost increases or penalties could result in significant reductions to revenue and margins on these 
contracts. The actual project results can be significantly different from the estimated results. When adjustments are identified 
near or at the end of a project, the full impact of the change in estimate is recognized in that period. This can result in a 
material impact on our results for a single reporting period. 

Software Development Costs
Costs incurred internally in creating computer software solutions and enhancements to those solutions are expensed until 
completion of a detailed program design, which is when we determine that technological feasibility has been established. 
Thereafter, all software development costs are capitalized until such time as the software solutions and enhancements are 
available  for  general  release,  and  the  capitalized  costs  subsequently  are  reported  at  the  lower  of  amortized  cost  or  net 
realizable value. 

Net realizable value is computed as the estimated gross future revenues from each software solution less the amount of 
estimated future costs of completing and disposing of that product. Because the development of projected net future revenues 
related to our software solutions used in our net realizable value computation is based on estimates, a significant reduction 
in our future revenues could impact the recovery of our capitalized software development costs. If we missed our estimates 
of net future revenues by 10%, the amount of our capitalized software development costs would not be impaired. 

Capitalized costs are amortized based on current and expected net future revenue for each software solution with minimum 
annual amortization equal to the straight-line amortization over the estimated economic life of the software solution. We are 
amortizing capitalized costs over five years. The five-year period over which capitalized software development costs are 
amortized is an estimate based upon our forecast of a reasonable useful life for the capitalized costs. Historically, use of our 
software programs by our clients has exceeded five years and is capable of being used a decade or more. 

We expect that major software information systems companies, large information technology consulting service providers 
and systems integrators and others specializing in the health care industry may offer competitive products or services. The 
pace of change in the HCIT market is rapid and there are frequent new product introductions, product enhancements and 
evolving industry standards and requirements. As a result, the capitalized software solutions may become less valuable or 
obsolete and could be subject to impairment. 

Goodwill
Goodwill is not amortized but is evaluated for impairment annually or whenever there is an impairment indicator. All goodwill 
is assigned to a reporting unit, where it is subject to an annual impairment assessment. We assess goodwill for impairment 
in the second quarter of each fiscal year and evaluate impairment indicators at each quarter end. We assessed our goodwill 
for impairment in the second quarters of 2014 and 2013 and concluded that goodwill was not impaired. The assessments 
consisted of a qualitative analysis in accordance with new guidance effective in 2012.  A key consideration in conducting 
those analyses was the growth in both the revenues and operating earnings of our reporting units since our last quantitative 
assessment.  Our last quantitative assessment was performed in 2011, in which the fair values of each of our reporting units 
exceeded their carrying amounts by a significant margin. We used a discounted cash flow analysis utilizing Level 3 inputs, 
to determine the fair value of the reporting units in 2011. Goodwill amounted to $320.5 million and $307.4 million at the end 
of 2014 and 2013, respectively. If future anticipated cash flows from our reporting units that recognized goodwill do not 
materialize as expected, our goodwill could be impaired, which could result in significant charges to earnings. 

Income Taxes
We make a number of assumptions and estimates in determining the appropriate amount of expense to record for income 
taxes.  These  assumptions  and  estimates  consider  the  taxing  jurisdictions  in  which  we  operate  as  well  as  current  tax 
regulations. Accruals are established for estimates of tax effects for certain transactions, business structures and future 
projected profitability of our businesses based on our interpretation of existing facts and circumstances. If these assumptions 
and estimates were to change as a result of new evidence or changes in circumstances, the change in estimate could result 
in a material adjustment to the consolidated financial statements. 

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We have discussed the development and selection of these critical accounting estimates with the Audit Committee of our 
Board of Directors and the Audit Committee has reviewed our disclosure contained herein. 

Item 7A. Quantitative and Qualitative Disclosures about Market Risk 

We use a foreign-currency denominated debt instrument to reduce our foreign currency exchange rate exposure in the U.K. 
As of the end of 2014, we designated all of our Great Britain Pound (GBP) denominated long-term debt (9.3 million GBP) 
as a net investment hedge of our U.K. operations. Because the borrowing is denominated in pounds, we are exposed to 
movements in the foreign currency exchange rate between the U.S. dollar (USD) and the GPB.  We estimate that a hypothetical 
10% adverse change in the foreign currency exchange rate between the USD and GBP would have impacted the unrealized 
loss, net of related income tax effects, of the net investment hedge recognized in other comprehensive income in 2014 by 
approximately $0.9 million, as compared to $1.9 million in 2013.  The 2014 model assumes an exchange rate of 1.533 at 
January 3, 2015 and a tax rate of 38.8%.  The hypothetical decrease in other comprehensive income in 2014 from 2013 is 
a result of a lower amount of GBP denominated debt outstanding.  Actual results may differ. Please refer to Notes (9) and 
(10)  to  the  Consolidated  Financial  Statements  for  a  more  detailed  discussion  of  the  foreign-currency  denominated  debt 
instrument. 

Item 8. Financial Statements and Supplementary Data 

The Financial Statements and Notes required by this Item are submitted as a separate part of this report.  See Note (20) to   
the Consolidated Financial Statements for supplementary financial information.

Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure 

N/A 

Item 9A. Controls and Procedures

a)  The Company’s Chief Executive Officer (CEO) and Chief Financial Officer (CFO) have evaluated the effectiveness 
of the Company’s disclosure controls and procedures (as defined in the Exchange Act Rules 13a-15(e) and 15d-15
(e)) as of the end of the period covered by this Annual Report (the Evaluation Date). They have concluded that, as 
of the Evaluation Date and based on the evaluation of these controls and procedures required by paragraph (b) of 
Exchange Act Rule 13a-15 or 15d-15, these disclosure controls and procedures were effective to ensure that material 
information relating to the Company and its consolidated subsidiaries would be made known to them by others within 
those entities and would be disclosed on a timely basis. The CEO and CFO have concluded that the Company’s 
disclosure controls and procedures are designed, and are effective, to give reasonable assurance that the information 
required to be disclosed by the Company in reports that it files under the Exchange Act is recorded, processed, 
summarized and reported within the time period specified in the rules and forms of the SEC. They have also concluded 
that the Company’s disclosure controls and procedures are effective to ensure that information required to be disclosed 
in the reports that are filed or submitted under the Exchange Act are accumulated and communicated to the Company’s 
management to allow timely decisions regarding required disclosure. 

b)  There were no changes in the Company’s internal controls over financial reporting during the three months ended 
January 3, 2015, that have materially affected, or are reasonably likely to materially affect, its internal controls over 
financial reporting. 

c)  The  Company’s  management,  including  its  CEO  and  CFO,  have  concluded  that  our  disclosure  controls  and 
procedures and internal control over financial reporting are designed to provide reasonable assurance of achieving 
their objectives and are effective at that reasonable assurance level. However, the Company’s management can 
provide no assurance that our disclosure controls and procedures or our internal control over financial reporting can 
prevent all errors and all fraud under all circumstances.  A control system, no matter how well conceived and operated, 
can provide only reasonable, not absolute, assurance that the objectives of the control system are met. Further, the 
design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must 
be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of 
controls can provide absolute assurance that all control issues and instances of fraud, if any, within the Company 
have been or will be detected. The design of any system of controls also is based in part upon certain assumptions 
about the likelihood of future events, and there can be no assurance that any design will succeed in achieving its 
stated goals under all potential future conditions; over time, controls may become inadequate because of changes 

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in conditions, or the degree of compliance with policies or procedures may deteriorate. Because of the inherent 
limitations in a cost-effective control system, misstatements due to error or fraud may occur and not be detected. 

Management’s Report on Internal Control over Financial Reporting 

The Company’s management is responsible for establishing and maintaining adequate internal control over financial reporting 
(as  defined  in  Rule  13a-15(f)  under  the  Securities  Exchange Act  of  1934,  as  amended).  The  Company’s  management 
assessed the effectiveness of the Company’s internal control over financial reporting as of January 3, 2015. In making this 
assessment, the Company’s management used the criteria set forth by the Committee of Sponsoring Organizations of the 
Treadway  Commission  (COSO)  in  its  Internal  Control-Integrated  Framework  (1992).  The  Company’s  management  has 
concluded that, as of January 3, 2015, the Company’s internal control over financial reporting is effective based on these 
criteria. The Company’s independent registered public accounting firm that audited the consolidated financial statements 
included in this annual report has issued an audit report on the effectiveness of the Company’s internal control over financial 
reporting, which is included herein under “Report of Independent Registered Public Accounting Firm”. 

Item 9B. Other Information

N/A

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PART III

Item 10. Directors, Executive Officers and Corporate Governance 

The information required by this Item 10 regarding our Directors and any nominees to become Directors will be set forth 
under the caption “Information Concerning Directors” in our Proxy Statement in connection with the 2015 Annual Shareholders’ 
Meeting scheduled to be held May 22, 2015 (the Proxy Statement), and is incorporated in this Item 10 by reference. The 
information required by this Item 10 regarding family relationships between any Director, Executive Officer or other person 
nominated to become a Director or Executive Officer will be set forth under the caption “Certain Transactions” in our Proxy 
Statement and is incorporated in this Item 10 by reference. The information required by this Item 10 concerning compliance 
with  Section  16(a)  of  the  Securities  Exchange Act  of  1934  will  be  set  forth  under  the  caption  “Section  16(a)  Beneficial 
Ownership Reporting Compliance” in our Proxy Statement and is incorporated in this Item 10 by reference.

The information required by this Item 10 concerning our Code of Business Conduct and Ethics will be set forth under the 
caption “Corporate Governance: Code of Business Conduct and Ethics” in our Proxy Statement and is incorporated in this 
Item 10 by reference. The information required by this Item 10 concerning our Audit Committee and our Audit Committee 
financial expert will be set forth under the caption “Committees of the Board: Audit Committee” in our Proxy Statement and 
is incorporated in this Item 10 by reference. 

There have been no material changes to the procedures by which security holders may recommend nominees to our Board 
of Directors since our last disclosure thereof. The information required by this Item 10 regarding our Executive Officers is set 
forth under the caption “Executive Officers of the Registrant” in Part I above. 

Item 11. Executive Compensation

The  information  required  by  this  Item  11  concerning  our  executive  compensation  will  be  set  forth  under  the  caption 
“Compensation  Discussion  and Analysis”  in  our  Proxy  Statement  and  is  incorporated  in  this  Item  11  by  reference.  The 
information  required  by  this  Item  11  concerning  Director  compensation  will  be  set  forth  under  the  caption  "Director 
Compensation" in our Proxy Statement and is incorporated in this Item 11 by reference.  The information required by this 
Item  11  concerning  Compensation  Committee  interlocks  and  insider  participation  will  be  set  forth  under  the  caption 
“Compensation Committee Interlocks and Insider Participation” in our Proxy Statement and is incorporated in this Item 11 
by reference. The information required by this Item 11 concerning Compensation Committee report will be set forth under 
the caption “Compensation Committee Report” in our Proxy Statement and is incorporated in this Item 11 by reference. 

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Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters 

The information required by this Item 12 will be set forth under the caption “Security Ownership of Certain Beneficial 
Owners and Management” in our Proxy Statement and is incorporated in this Item 12 by reference. 

The following table provides information about our common stock that may be issued under our equity compensation 
plans as of January 3, 2015: 

(In thousands, except per share data)

Plan category

Equity compensation plans approved by 
security holders (4)
Equity compensation plans not approved by
security holders

Total

Securities to 
be issued 
upon 
exercise of 
outstanding 
options and 
rights (1)

Weighted 
average 
exercise 
price per 
share (2)

Securities 
available for 
future 
issuance(3)

25,135

$

27.00

—

25,135

—

8,080

—

8,080

(1) Includes grants of stock options, time-based and performance-based restricted stock.

(2) Includes weighted-average exercise price of outstanding stock options only. 

(3) Excludes securities to be issued upon exercise of outstanding options and rights.

(4) Includes the Stock Option Plan D, Stock Option Plan E, 2001 Long-Term Incentive Plan F, 2004 Long-Term Incentive Plan G and 2011 Omnibus Equity Incentive Plan. All new grants are 

made under the 2011 Omnibus Equity Incentive Plan, as the previous plans are no longer active.

All other information required by this Item is incorporated by reference from the Proxy Statement under the section entitled 
“Principal Security Ownership and Certain Beneficial Owners.”

Item 13. Certain Relationships and Related Transactions, and Director Independence 

The information required by this Item 13 concerning our transactions with related parties will be set forth under the caption 
“Certain Transactions” in our Proxy Statement and is incorporated in this Item 13 by reference. The information required by 
this Item 13 concerning director independence will be set forth under the caption “Meetings of the Board and Committees” 
in our Proxy Statement and is incorporated in this Item 13 by reference. 

Item 14. Principal Accountant Fees and Services

The information required by this Item 14 will be set forth under the caption “Relationship with Independent Registered Public 
Accounting Firm” in our Proxy Statement and is incorporated in this Item 14 by reference. 

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PART IV 

Item 15. Exhibits and Financial Statement Schedules 

a)  Financial Statements and Exhibits

(1)  Consolidated Financial Statements:

Reports of Independent Registered Public Accounting Firm

Consolidated Balance Sheets - As of January 3, 2015 and December 28, 2013 

Consolidated Statements of Operations -Years Ended January 3, 2015, December 28, 2013 and 
December 29, 2012 

Consolidated Statements of Comprehensive Income - Years Ended January 3, 2015, 
December 28, 2013 and December 29, 2012

Consolidated Statements of Cash Flows -  Years Ended January 3, 2015, December 28, 2013 
and December 29, 2012

Consolidated Statements of Changes in Shareholders' Equity - Years Ended January 3, 2015, 
December 28, 2013 and December 29, 2012

Notes to Consolidated Financial Statements

(2)  The following financial statement schedule and Report of Independent Registered Public Accounting Firm 

of the Registrant for the three-year period ended January 3, 2015 are included herein: 

Schedule  II—Valuation  and  Qualifying  Accounts,  Report  of  Independent  Registered  Public 
Accounting Firm

All other schedules  are omitted, as the  required  information  is  inapplicable  or the information  is 
presented in the consolidated financial statements or related notes. 

(3)  See the Index to Exhibits immediately following the signature page of this Annual Report on Form 10-K.

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SIGNATURES

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. 

Date: February 11, 2015

CERNER CORPORATION

By:

/s/ Neal L. Patterson                   
Neal L. Patterson
Chairman of the Board and
Chief Executive Officer

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 and Title

Date

/s/ Neal L. Patterson

February 11, 2015

Neal L. Patterson, Chairman of the Board and Chief
Executive Officer (Principal Executive Officer)

/s/ Clifford W. Illig

February 11, 2015

Clifford W. Illig, Vice Chairman and Director

/s/ Marc G. Naughton

February 11, 2015

Marc G. Naughton, Executive Vice President and
Chief Financial Officer (Principal Financial Officer)

/s/ Michael R. Battaglioli

February 11, 2015

Michael R. Battaglioli, Vice President and
Chief Accounting Officer (Principal Accounting Officer)

/s/ Gerald E. Bisbee, Jr.

Gerald E. Bisbee, Jr., Ph.D., Director

/s/ Denis A. Cortese, M.D.

Denis A. Cortese, M.D., Director

/s/ John C. Danforth

John C. Danforth, Director

/s/ Mitchell E. Daniels

Mitchell E. Daniels, Director

/s/ Linda M. Dillman

Linda M. Dillman, Director

/s/ William B. Neaves

William B. Neaves, Ph.D., Director

/s/ William D. Zollars

William D. Zollars, Director

February 11, 2015

February 11, 2015

February 11, 2015

February 11, 2015

February 11, 2015

February 11, 2015

February 11, 2015

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INDEX TO EXHIBITS

Incorporated by Reference

Exhibit 
Number

Exhibit Description

Form

Exhibit(s)

Filing Date 
SEC File No./Film No.

Filed
Herewith

8-K

3.2

12/23/2013

X

Cerner Corporation 2001 Long-Term Incentive Plan F

DEF 14A

Annex I

3(a)

3(b)

4(a)

10.1*

10.2*

10.3*

10.4*

10.5*

10.6*

10.7*

10.8*

10.9*

10.10*

10.11*

10.12*

10.13*

10.14*

10.15*

10.16*

10.17*

Third  Restated  Certificate  of 
September 12, 2013

Incorporation  dated 

Amended & Restated Bylaws as of September 16, 2008 
(as  amended  March  31,  2010,  March  9,  2011  and 
December 23, 2013)

Specimen stock certificate

2006  Form  of  Indemnification  Agreement  for  use 
between the Registrant and its Directors

2010  Form  of  Indemnification  Agreement  for  use 
between the Registrant and its Directors and Section 16 
Officers

Amended  &  Restated  Executive  Employment 
Agreement of Neal L. Patterson dated January 1, 2008

Amended  Stock  Option  Plan  D  of  Registrant  dated 
December 8, 2000

Amended  Stock  Option  Plan  E  of  Registrant  dated 
December 8, 2000

Cerner Corporation 2001 Long-Term Incentive Plan F 
Nonqualified Stock Option Agreement

Cerner Corporation 2001 Long-Term Incentive Plan F 
Nonqualified Stock Option Grant Certificate

Cerner Corporation 2001 Long-Term Incentive Plan F 
Director Restricted Stock Agreement

Cerner Corporation 2001 Long-Term Incentive Plan F 
Nonqualified Stock Option Director Agreement

Cerner Corporation 2001 Long-Term Incentive Plan F 
Performance-Based  Restricted  Stock  Agreement  for 
Section 16 Officers

Cerner Corporation 2004 Long-Term Incentive Plan G 
(as amended on December 3, 2007)

Cerner Corporation 2004 Long-Term Incentive Plan G 
Nonqualified Stock Option Grant Certificate

Cerner Corporation 2011 Omnibus Equity Incentive Plan

Cerner Corporation 2011 Omnibus Equity Incentive Plan 
- Director Restricted Stock Agreement

Cerner Corporation 2011 Omnibus Equity Incentive Plan 
- Performance Based Restricted Stock Agreement

Cerner  Corporation  2011  Omnibus  Equity  Incentive 
Plan-Non-Qualified Stock Option Grant Certificate

59
40

10-K

4(a)

10-K

10(a)

8-K

99.1

10-K

10(c)

10-K

10(f)

10-K

10(g)

10-K

10(v)

10-Q

10(a)

10-K

10(x)

10-K

10(w)

8-K

99.1

2/28/2007
000-15386/07658265

2/28/2007
000-15386/07658265

6/3/2010
000-15386/10875957

2/27/2008
000-15386/08646565

3/30/2001
000-15386/1586224

3/30/2001
000-15386/1586224

4/16/2001
000-15386/1603080

3/17/2005
000-15386/05688830

11/10/2005
000-15386/051193974

3/17/2005
000-15386/05688830

3/17/2005
000-15386/05688830

6/4/2010
000-15386/10879084

10-K

10(g)

10-K

10(q)

S-8

10-Q

4.5

10.1

2/27/2008
000-15386/08646565

2/27/2008
000-15386/08646565

5/27/2011

7/27/2012

10-K

10(u)

2/8/2013

10-K

10(v)

2/8/2013

Table of Contents

10.18*

10.19*

10.20*

10.21*

10.22*

10.23*

10.24*

10.25

10.26

10.27

10.28

10.29

10.30

10.31

10.32

10.33

10.34

Cerner  Corporation  2001  Associate  Stock  Purchase 
Plan as Amended and Restated March 1, 2010 and May 
27, 2011

Cerner Corporation Performance-Based Compensation 
Plan (as Amended and Restated March 5, 2014)

Form of 2014 Executive Performance Agreement

Cerner Corporation Executive Deferred Compensation 
Plan as Amended & Restated dated January 1, 2008

Cerner  Corporation  2005  Enhanced  Severance  Pay 
Plan  as  Amended  &  Restated  (for  I.R.C.  §  409A) 
Effective December 31, 2012

Cerner  Corporation  2005  Enhanced  Severance  Pay 
Plan  as  Amended  &  Restated  (for  I.R.C.  §  409A) 
Effective January 4, 2015

Exhibit A Severance Matrix, effective April 1, 2011 to the 
Cerner  Corporation  2005  Enhanced  Severance  Pay 
Plan as Amended & Restated dated August 15, 2010

Second Amended and Restated Aircraft Time Sharing 
Agreement  between  Cerner  Corporation  and  Neal  L. 
Patterson dated July 24, 2013

Interparty Agreement, dated January 19, 2010, among 
Kansas Unified Development, LLC, OnGoal, LLC and 
Cerner Corporation

Real  Estate  Purchase  Agreement  between  Cerner 
Property Development, Inc. and Trails Property II, Inc. 
dated July 30, 2013

First Amendment to Real Estate Purchase Agreement 
between Cerner Property Development, Inc. and Trails 
Property II, Inc. dated December 23, 2013

Second  Amendment 
to  Real  Estate  Purchase 
Agreement between Cerner Property Development, Inc. 
and Trails Property II, Inc. dated October 16, 2014

Master  Sale  and  Purchase  Agreement  between 
Siemens AG and Cerner Corporation dated August 5, 
2014

Amendment  Agreement 
the  Master  Sale  and 
to 
Purchase Agreement between Siemens AG and Cerner 
Corporation dated February 2, 2015

Note Purchase Agreement, dated November 1, 2005, 
among Cerner Corporation, as issuer, and AIG Annuity 
Insurance Company, American General Life Insurance 
Company  and  Principal  Life  Insurance  Company,  as 
purchasers

Master  Note  Purchase  Agreement  between  Cerner 
Corporation  and  the  Purchasers  listed  in  Schedule A 
thereto dated December 4, 2014

Amended  and  Restated  Credit  Agreement,  dated 
February 10, 2012, among Cerner Corporation and U.S. 
Bank  National  Association,  Bank  of  America,  N.A., 
Commerce  Bank,  N.A.,  UMB  Bank,  N.A.  and  RBS 
Citizens, N.A.

60
41

X

X

X

X

S-8

4.6

5/27/2011

10-Q

10-K

10.1

10(k)

4/25/2014

2/27/2008
000-15386/08646565

10-K

10(l)

2/8/2013

10-Q

10(a)

4/29/2011

10-Q

10.1

7/26/2013

8-K

99.1

1/22/2010
000-153866/10543089

8-K

10.1

8/1/2013

10-Q

2.1

10/24/2014

8-K

10.1

2/2/2015

8-K

99.1

11/7/2005
000-15386/051183275

8-K

10.1

12/5/2014

8-K

99.1

2/13/2012
000-15386/12599122

Table of Contents

10.35

10.36

21

23

31.1

31.2

32.1

32.2

First  Amendment  to  Amended  and  Restated  Credit 
Agreement, dated December 28, 2012, among Cerner 
Corporation and U.S. Bank National Association, Bank 
of America, N.A.,  Commerce  Bank,  N.A.,  UMB  Bank, 
N.A. and RBS Citizens, N.A.

Second Amendment to Amended and Restated Credit 
Agreement,  dated  January  15,  2015,  among  Cerner 
Corporation and U.S. Bank National Association, Bank 
of America, N.A.,  Commerce  Bank,  N.A.,  UMB  Bank, 
N.A. and RBS Citizens, N.A.

Subsidiaries of Registrant

Consent of Independent Registered Public Accounting 
Firm

Certification of Neal L. Patterson pursuant to Section 302 
of Sarbanes-Oxley Act of 2002

Certification of Marc G. Naughton pursuant to Section 
302 of Sarbanes-Oxley Act of 2002

Certification of Neal L. Patterson pursuant to 18 U.S.C. 
Section 1350, as adopted pursuant to Section 906  of 
Sarbanes-Oxley Act of 2002

Certification of Marc G. Naughton pursuant to 18 U.S.C. 
Section 1350, as adopted pursuant to Section 906  of 
Sarbanes-Oxley Act of 2002

101.INS

XBRL Instance Document

101.SCH

XBRL Taxonomy Extension Schema Document

101.CAL

101.LAB

101.PRE

101.DEF

XBRL Taxonomy Extension Calculation Linkbase
Document

XBRL Taxonomy Extension Labels Linkbase
Document

XBRL Taxonomy Extension Presentation Linkbase
Document

XBRL Taxonomy Extension Definition Linkbase
Document

10-K

4(c)

2/8/2013

X

X

X

X

X

X

X

X

X

X

X

X

X

*  Indicates a management contract or compensatory plan or arrangement required to be identified by Part IV, Item 15(a)(3).

61
42

Table of Contents

Report of Independent Registered Public Accounting Firm

The Board of Directors and Shareholders 
Cerner Corporation: 

We have audited Cerner Corporation and subsidiaries’ internal control over financial reporting as of January 3, 2015, based 
on criteria established in Internal Control - Integrated Framework (1992) issued by the Committee of Sponsoring Organizations 
of the Treadway Commission (COSO). Cerner Corporation and subsidiaries’ 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 Cerner Corporation and subsidiaries’ 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, and testing and evaluating the 
design and operating effectiveness of internal control based on the assessed risk. Our audit also included 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 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 its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, 
projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate 
because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.

In our opinion, Cerner Corporation and subsidiaries maintained, in all material respects, effective internal control over financial 
reporting as of January 3, 2015, based on criteria established in Internal Control - Integrated Framework (1992) issued by 
the Committee of Sponsoring Organizations of the Treadway Commission (COSO).

We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), 
the consolidated balance sheets of Cerner Corporation and subsidiaries as of January 3, 2015 and December 28, 2013, and 
the related consolidated statements of operations, comprehensive income, cash flows, and changes in shareholders’ equity 
for each of the years in the three-year period ended January 3, 2015, and our report dated February 11, 2015 expressed an 
unqualified opinion on those consolidated financial statements. 

/s/KPMG LLP 
Kansas City, Missouri 
February 11, 2015 

43
62

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Report of Independent Registered Public Accounting Firm

The Board of Directors and Shareholders 
Cerner Corporation: 

We have audited the accompanying consolidated balance sheets of Cerner Corporation and subsidiaries as of  January 3, 
2015 and December 28, 2013, and the related consolidated statements of operations, comprehensive income, cash flows, 
and changes in shareholders’ equity for each of the years in the three-year period ended January 3, 2015. These consolidated 
financial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on 
these consolidated financial statements 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 consolidated financial statements referred to above present fairly, in all material respects, the financial 
position  of  Cerner  Corporation  and  subsidiaries  as  of  January 3,  2015  and  December 28,  2013,  and  the  results  of  their 
operations and their cash flows for each of the years in the three-year period ended January 3, 2015, in conformity with U.S. 
generally accepted accounting principles.

We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), 
Cerner  Corporation  and  subsidiaries’  internal  control  over  financial  reporting  as  of  January 3,  2015,  based  on  criteria 
established in Internal Control - Integrated Framework (1992) issued by the Committee of Sponsoring Organizations of the 
Treadway Commission (COSO), and our report dated February 11, 2015 expressed an unqualified opinion on the effectiveness 
of Cerner Corporation and subsidiaries’ internal control over financial reporting.

/s/KPMG LLP 
Kansas City, Missouri 
February 11, 2015 

44
63

Table of Contents

CERNER CORPORATION AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
As of January 3, 2015 and December 28, 2013 

(In thousands, except share data)

Assets

Current assets:

Cash and cash equivalents
Short-term investments
Receivables, net
Inventory
Prepaid expenses and other
Deferred income taxes, net
Total current assets

Property and equipment, net
Software development costs, net
Goodwill
Intangible assets, net
Long-term investments
Other assets

Total assets

Liabilities and Shareholders’ Equity

Current liabilities:

Accounts payable
Current installments of long-term debt and capital lease obligations
Deferred revenue
Accrued payroll and tax withholdings
Other accrued expenses
Total current liabilities

Long-term debt and capital lease obligations
Deferred income taxes and other liabilities
Deferred revenue
Total liabilities

Shareholders’ Equity:

Common stock, $.01 par value, 500,000,000 shares authorized, 346,985,811 shares issued at January 3, 

2015 and 344,338,030 shares issued at December 28, 2013

Additional paid-in capital
Retained earnings
Treasury stock, 4,652,515 shares at January 3, 2015 and 570,616 shares at December 28, 2013
Accumulated other comprehensive loss, net

Total shareholders’ equity

Total liabilities and shareholders’ equity

See notes to consolidated financial statements.

64
45

2014

2013

$ 635,203
785,663
672,778
23,789
209,278
22,075
2,348,786

$ 202,377
677,004
582,926
32,299
175,488
91,614
1,761,708

924,260
420,199
320,538
126,636
231,147
158,999

792,781
347,077
307,422
144,132
554,873
190,371

$ 4,530,565

$ 4,098,364

$ 160,285
67,460
209,655
140,230
56,685
634,315

$ 145,019
54,107
209,746
147,986
83,574
640,432

62,868
256,601
10,813
964,597

111,717
170,392
8,159
930,700

3,470
933,446
2,918,481
(245,333)
(44,096)
3,565,968

3,443
812,853
2,393,048
(28,251)
(13,429)
3,167,664

$ 4,530,565

$ 4,098,364

Table of Contents

CERNER CORPORATION AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF OPERATIONS
For the years ended January 3, 2015, December 28, 2013 and December 29, 2012 

(In thousands, except per share data)

Revenues:

System sales

Support, maintenance and services

Reimbursed travel

Total revenues

Costs and expenses:

Cost of system sales

Cost of support, maintenance and services

Cost of reimbursed travel

Sales and client service

Software development (Includes amortization of $103,447, $94,688 and $81,731, respectively)

General and administrative

Total costs and expenses

Operating earnings

Other income, net

Earnings before income taxes

Income taxes

Net earnings

Basic earnings per share

Diluted earnings per share

Basic weighted average shares outstanding

Diluted weighted average shares outstanding

See notes to consolidated financial statements.

For the Years Ended
2013

2012

2014

$ 945,858

$ 847,809

$ 902,799

2,366,959

1,992,830

1,707,329

89,886

70,109

55,308

3,402,703

2,910,748

2,665,436

314,089

200,402

89,886

302,374

142,239

70,109

427,456

125,433

55,308

1,395,568

1,173,051

1,020,640

392,805

246,869

338,786

308,177

301,370

163,567

2,639,619

2,334,736

2,093,774

763,084

576,012

571,662

11,090

12,042

16,046

774,174

588,054

587,708

(248,741)

(189,700)

(190,476)

$ 525,433

$ 398,354

$ 397,232

$

$

1.54

1.50

$

$

1.16

1.13

$

$

1.16

1.13

342,150

343,636

341,861

350,386

352,281

351,394

46
65

 
 
Table of Contents

CERNER CORPORATION AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME
For the years ended January 3, 2015, December 28, 2013 and December 29, 2012 

(In thousands)

Net earnings

Foreign currency translation adjustment and other (net of tax benefits of $1,111, $3,604 and $1,396,

respectively)

Change in net unrealized holding gain (loss) on available-for-sale investments (net of taxes (benefits) of

$(331), $10 and $125, respectively)

Comprehensive income

See notes to consolidated financial statements.

For the Years Ended
2013

2012

2014

$ 525,433

$ 398,354

$ 397,232

(30,145)

(8,185)

6,511

(522)

11

201

$ 494,766

$ 390,180

$ 403,944

47
66

 
 
Table of Contents

CERNER CORPORATION AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CASH FLOWS
For the years ended January 3, 2015, December 28, 2013 and December 29, 2012 

(In thousands)
CASH FLOWS FROM OPERATING ACTIVITIES:
Net earnings
Adjustments to reconcile net earnings to net cash provided by operating activities:

Depreciation and amortization
Share-based compensation expense
Provision for deferred income taxes

Changes in assets and liabilities (net of businesses acquired):

Receivables, net
Inventory
Prepaid expenses and other
Accounts payable
Accrued income taxes
Deferred revenue
Other accrued liabilities

Net cash provided by operating activities

CASH FLOWS FROM INVESTING ACTIVITIES:

Capital purchases
Capitalized software development costs
Purchases of investments
Sales and maturities of investments
Purchase of other intangibles
Acquisition of businesses, net of cash acquired

Net cash used in investing activities

CASH FLOWS FROM FINANCING ACTIVITIES:

Repayment of long-term debt and capital lease obligations
Proceeds from excess tax benefits from share-based compensation
Proceeds from exercise of options
Treasury stock purchases
Contingent consideration payments for acquisition of businesses
Cash grants
Other

Net cash provided by (used in) financing activities

Effect of exchange rate changes on cash and cash equivalents

Net increase (decrease) in cash and cash equivalents
Cash and cash equivalents at beginning of period

Cash and cash equivalents at end of period

Supplemental disclosures of cash flow information

Cash paid during the year for:

Interest
Income taxes, net of refunds
Summary of acquisition transactions:

Fair value of net tangible assets (liabilities) acquired (assumed)
Fair value of intangible assets acquired
Fair value of goodwill
Less: Fair value of contingent liability payable

Cash paid for acquisitions

Cash acquired

Net cash used

See notes to consolidated financial statements.

48
67

For the Years Ended
2013

2012

2014

$ 525,433

$ 398,354

$ 397,232

302,353
59,292
106,905

(74,786)
8,117
(14,625)
2,974
(21,764)
4,346
(51,218)

263,538
46,295
(22,647)

(9,599)
(8,111)
(36,038)
4,130
14,694
18,053
27,196

222,580
36,113
8,342

(83,705)
(279)
(2,224)
35,265
(22,784)
33,277
84,497

847,027

695,865

708,314

(276,584)
(177,800)
(1,214,036)
1,404,846
(13,517)
(7,476)

(352,877)
(174,649)
(1,106,819)
1,070,598
(56,805)
(67,877)

(183,429)
(100,189)
(1,286,997)
932,394
(22,870)
(40,540)

(284,567)

(688,429)

(701,631)

(14,930)
39,532
31,879
(217,082)
(10,617)
48,000
2,894

(24,700)
39,927
31,403
(170,042)
(800)
—
4,823

(120,324)

(119,389)

(9,310)

(2,790)

432,826
202,377

(114,743)
317,120

(17,083)
48,370
38,147
—
(3,400)
—
—

66,034

1,257

73,974
243,146

$ 635,203

$ 202,377

$ 317,120

$

$

5,682
144,323

$

6,973
175,377

(1,509) $
3,800
16,785
(11,600)
7,476
—

2,550
25,489
59,570
(18,982)
68,627
(750)

$

$

6,448
158,871

(6,375)
18,559
35,281
(1,916)
45,549
(5,009)

$

7,476

$

67,877

$

40,540

Table of Contents

CERNER CORPORATION AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS' EQUITY
For the years ended January 3, 2015, December 28, 2013 and December 29, 2012

(In thousands)

Common Stock

Additional

Retained

Treasury

Shares

Amount

Paid-in Capital

Earnings

Stock

Accumulated
Other

Noncont
rolling

Comprehensiv
e Income
(Loss)

Interest

Balance at December 31, 2011

339,132

$ 3,392

$

721,794

$

1,597,462

$

— $

(11,967) $

120

Exercise of stock options (including net-settled option exercises)

5,047

Employee share-based compensation expense

Employee share-based compensation net excess tax benefit

Other comprehensive income (loss)

Dissolution of underlying entity

Net earnings

—

—

—

—

—

50

—

—

—

—

—

32,536

36,113

50,326

—

—

—

—

—

—

—

—

397,232

Balance at December 29, 2012

344,179

3,442

840,769

1,994,694

Exercise of stock options (including net-settled option exercises)

3,204

Employee share-based compensation expense

Employee share-based compensation net excess tax benefit

Other comprehensive income (loss)

Treasury stock purchases

Distribution of treasury stock in stock split

Net earnings

—

—

—

—

(3,045)

—

32

—

—

—

—

(31)

—

27,056

46,295

40,493

—

—

(141,760)

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

(170,042)

141,791

—

398,354

—

—

—

—

6,712

—

—

(5,255)

—

—

—

(8,174)

—

—

—

Balance at December 28, 2013

344,338

3,443

812,853

2,393,048

(28,251)

(13,429)

Exercise of stock options (including net-settled option exercises)

2,648

Employee share-based compensation expense

Employee share-based compensation net excess tax benefit

Other comprehensive income (loss)

Treasury stock purchases

Net earnings

—

—

—

—

—

27

—

—

—

—

—

21,613

59,292

39,688

—

—

—

—

—

—

—

—

—

—

—

—

(217,082)

525,433

—

—

—

—

(30,667)

—

—

Balance at January 3, 2015

346,986

$ 3,470

$

933,446

$

2,918,481

$

(245,333) $

(44,096) $

See notes to consolidated financial statements.

49
68

—

—

—

—

(120)

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

—

Table of Contents

CERNER CORPORATION AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

(1) Basis of Presentation, Nature of Operations and Summary of Significant Accounting Policies

Basis of Presentation 

The consolidated financial statements include all the accounts of Cerner Corporation (Cerner, the Company, we, us or our) 
and its subsidiaries. All significant intercompany transactions have been eliminated in consolidation. 

The consolidated financial statements were prepared using accounting principles generally accepted in the United States. 
These principles require us to make estimates and assumptions that affect the reported amounts of assets and liabilities, 
the disclosure of contingent assets and liabilities and the reported amounts of revenues and expenses. Actual results could 
differ from those estimates. 

Our fiscal year ends on the Saturday closest to December 31. Fiscal year 2014 consisted of 53 weeks and ended on January 3, 
2015, and fiscal years 2013 and 2012 consisted of 52 weeks each and ended on December 28, 2013 and December 29, 
2012, respectively.  All references to years in these notes to consolidated financial statements represent fiscal years unless 
otherwise noted. 

Nature of Operations 

We design, develop, market, install, host and support health care information technology, health care devices, hardware and 
content  solutions  for  health  care  organizations  and  consumers.  We  also  provide  a  wide  range  of  value-added  services, 
including implementation and training, remote hosting, operational management services, revenue cycle services, support 
and maintenance, health care data analysis, clinical process optimization, transaction processing, employer health centers, 
employee wellness programs and third party administrator services for employer-based health plans. 

Summary of Significant Accounting Policies 

(a) Revenue Recognition - We recognize software related revenue in accordance with the provisions of Accounting Standards 
Codification (ASC) 985-605, Software – Revenue Recognition and non-software related revenue in accordance with ASC 
605, Revenue Recognition. In general, revenue is recognized when all of the following criteria have been met:

•  Persuasive evidence of an arrangement exists;

•  Delivery has occurred or services have been rendered;

•  Our fee is fixed or determinable; and

•  Collection of the revenue is reasonably assured.

The following are our major components of revenue:

•  System sales – includes the licensing of computer software, software as a service, deployment period upgrades, 
installation, content subscriptions, transaction processing and the sale of computer hardware and sublicensed 
software;

•  Support, maintenance and service – includes software support and hardware maintenance, remote hosting and 

managed services, training, consulting and implementation services; and

•  Reimbursed travel – includes reimbursable out-of-pocket expenses (primarily travel) incurred in connection with 

our client service activities.

We provide for several models of procurement of our information systems and related services. The predominant model 
involves multiple deliverables  and includes a perpetual software  license agreement, project-related  installation services, 
implementation and consulting services, software support and either hosting services or computer hardware and sublicensed 
software, which requires that we allocate revenue to each of these elements. 

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69

 
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Allocation of Revenue to Multiple Element Arrangements

For multiple element arrangements that contain software and non-software elements, we allocate revenue to software and 
software-related elements as a group and any non-software element separately. After the arrangement consideration has 
been allocated to the non-software elements, revenue is recognized when the basic revenue recognition criteria are met for 
each element. For the group of software and software-related elements, revenue is recognized under the guidance applicable 
to software transactions. 

Since we do not have vendor specific objective evidence (VSOE) of fair value on software licenses within our multiple element 
arrangements, we recognize revenue on our software and software-related elements using the residual method. Under the 
residual method, license revenue is recognized in a multiple-element arrangement when vendor-specific objective evidence 
of fair value exists for all of the undelivered elements in the arrangement, when software is delivered, installed and all other 
conditions  to  revenue  recognition  are  met.  We  allocate  revenue  to  each  undelivered  element  in  a  multiple-element 
arrangement based on the element’s respective fair value, with the fair value determined by the price charged when that 
element  is  sold  separately.  Specifically,  we  determine  the  fair  value  of  the  software  support,  hardware  maintenance, 
sublicensed software support, remote hosting, subscriptions and software as a service portions of the arrangement based 
on the substantive renewal price for these services charged to clients; professional services (including training and consulting) 
portion of the arrangement, other than installation services, based on hourly rates which we charge for these services when 
sold apart from a software license; and sublicensed software based on its price when sold separately from the software. The 
residual amount of the fee after allocating revenue to the fair value of the undelivered elements is attributed to the licenses 
for software solutions, including project-related installation services. If evidence of the fair value cannot be established for 
the  undelivered  elements  of  a  license  agreement  using  VSOE,  the  entire  amount  of  revenue  under  the  arrangement  is 
deferred until these elements have been delivered or VSOE of fair value can be established. 

We also enter into arrangements that include multiple non-software deliverables. For each element in a multiple element 
arrangement  that  does  not  contain  software-related  elements  to  be  accounted  for  as  a  separate  unit  of  accounting,  the 
following  must  be  met:  the  delivered  products  or  services  have  value  to  the  client  on  a  stand-alone  basis;  and  for  an 
arrangement that includes a general right of return relative to the delivered products or services, delivery or performance of 
the undelivered product or service is considered probable and is substantially controlled by the Company.  We allocate the 
arrangement consideration to each element based on the selling price hierarchy of VSOE of fair value, if it exists, or third-
party  evidence  (TPE)  of  selling  price.  If  neither  VSOE  nor  TPE  are  available,  we  use  estimated  selling  price. After  the 
arrangement consideration has been allocated to the elements, we account for each respective element in the arrangement 
as described below.

For certain arrangements, revenue for software, implementation services and, in certain cases, support services for which 
VSOE of fair value cannot be established are accounted for as a single unit of accounting. The revenue recognized from 
single units of accounting are typically allocated and classified as system sales and support, maintenance and services. If 
available, the VSOE of fair value of the services provides the basis for support, maintenance and services allocation, and 
the remaining residual consideration provides the basis for system sales revenue allocations. In cases where VSOE cannot 
be established, revenue is classified based on the nature of related costs incurred. 

Revenue Recognition Policies for Each Element 

We provide project-related installation services when licensing our software solutions, which include project-scoping services, 
conducting pre-installation audits and creating initial environments. We have deemed installation services to be essential to 
the functionality of the software and, therefore, recognize the software license over the software installation period using the 
percentage-of-completion method. We measure the percentage-of-completion based on output measures that reflect direct 
labor hours incurred, beginning at software delivery and culminating at completion of installation. Installation generally occurs 
in the same period the contracts are executed but in the past has been extended over a longer period of time depending on 
client specific factors. 

We provide implementation and consulting services. These services vary depending on the scope and complexity of the 
engagement. Examples of such services may include database consulting, system configuration, project management, testing 
assistance,  network  consulting,  post  conversion  review  and  application  management  services.  Except  for  limited 
arrangements where our software requires significant modifications or customization, implementation and consulting services 
generally are not deemed to be essential to the functionality of the software and, thus, do not impact the timing of the software 
license recognition. However, if software license fees are tied to implementation milestones, then the portion of the software 
license fee tied to implementation milestones is deferred until the related milestone is accomplished and related fees become 

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due and payable and non-forfeitable. Implementation fees are recognized over the service period, which may extend from 
nine months to several years for multi-phased projects. 

Remote hosting and managed services are marketed under long-term arrangements generally over periods of five to 10 
years. These services are typically provided to clients that have acquired a perpetual license for licensed software and have 
contracted with us to host the software in our data center. Under these arrangements, the client generally has the contractual 
right to take possession of the licensed software at any time during the hosting period without significant penalty and it is 
feasible for the client to either run the software on its own equipment or contract with another party unrelated to us to host 
the software. Additionally, these services are not deemed to be essential to the functionality of the licensed software or other 
elements of the arrangement and as such, we allocate a portion of the services fee to the software and recognize it once 
the client has the ability to take possession of the software. The remaining services fee in these arrangements, as well as 
the services fee for arrangements where the client does not have the contractual right or the ability to take possession of the 
software at any time, is generally recognized ratably over the hosting service period.

We also offer our solutions on a software as a service model, providing time-based licenses for our software solutions available 
within an environment that we manage from our data centers. The data centers provide system and administrative support 
as well as processing services. Revenue on these services is combined and recognized on a monthly basis over the term 
of  the  contract.  We  capitalize  related  pre-contract  direct  set-up  costs  consisting  of  third  party  costs  and  direct  software 
installation and implementation costs associated with the initial set up of a software as a service client. These costs are 
amortized over the term of the arrangement.

Software support fees are marketed under annual and multi-year arrangements and are recognized as revenue ratably over 
the contractual support term. Hardware and sublicensed software maintenance revenues are recognized ratably over the 
contractual maintenance term.

Subscription and content fees are generally marketed under annual and multi-year agreements and are recognized ratably 
over the contractual terms.

Hardware and sublicensed software sales are generally recognized when title and risk of loss have transferred to the client. 

The sale of equipment under sales-type leases is recorded as system sales revenue at the inception of the lease. Sales-
type leases also produce financing income, which is included in system sales revenue and is recognized at consistent rates 
of return over the lease term.

Where we have contractually agreed to develop new or customized software code for a client, we utilize percentage-of-
completion accounting, labor-hours method.

Revenue generally is recognized net of any taxes collected from clients and subsequently remitted to governmental authorities. 

Payment Arrangements

Our payment arrangements with clients typically include an initial payment due upon contract signing and date-based licensed 
software payment terms and payments based upon delivery for services, hardware and sublicensed software. Revenue 
recognition on support payments received in advance of the services being performed are deferred and classified as either 
current or long term deferred revenue depending on whether the revenue will be earned within one year. 

We have periodically provided long-term financing options to creditworthy clients through third party financing institutions 
and have directly provided extended payment terms to clients from contract date. These extended payment term arrangements 
typically provide for date based payments over periods ranging from 12 months up to seven years. As a significant portion 
of the fee is due beyond one year, we have analyzed our history with these types of arrangements and have concluded that 
we have a standard business practice of using extended payment term arrangements and a long history of successfully 
collecting under the original payment terms for arrangements with similar clients, product offerings, and economics without 
granting  concessions. Accordingly,  we  consider  the  fee  to  be  fixed  and  determinable  in  these  extended  payment  term 
arrangements and, thus, the timing of revenue is not impacted by the existence of extended payments. 

Some of these payment streams have been assigned on a non-recourse basis to third party financing institutions. We account 
for the assignment of these receivables as sales of financial assets. Provided all revenue recognition criteria have been met, 

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we recognize revenue for these arrangements under our normal revenue recognition criteria, and if appropriate, net of any 
payment discounts from financing transactions. 

(b) Cash Equivalents - Cash equivalents consist of short-term marketable securities with original maturities less than 90 
days. 

(c) Investments – Our short-term investments are primarily invested in time deposits, commercial paper, government and 
corporate bonds, with maturities of less than one year.  Our long-term investments are primarily invested in government and 
corporate bonds with maturities of less than two years.  All of our investments, other than a small portion accounted for under 
the cost and equity methods, are classified as available-for-sale.

Available-for-sale securities are recorded at fair value with the unrealized gains and losses reflected in accumulated other 
comprehensive income until realized. Realized gains and losses from the sale of available-for-sale securities, if any, are 
determined on a specific identification basis. 

We regularly review investment securities for impairment based on both quantitative and qualitative criteria that include the 
extent to which cost exceeds fair value, the duration of any market decline, and the financial health of and specific prospects 
for the issuer. Unrealized losses that are other than temporary are recognized in earnings.

Premiums are amortized and discounts are accreted over the life of the security as adjustments to interest income for our 
investments. Interest income is recognized when earned. 

Refer to Note (3) and Note (4) for further description of these assets and their fair value. 

(d) Concentrations - The majority of our cash and cash equivalents are held at three major financial institutions. The majority 
of our cash equivalents consist of money market funds and commercial paper. Deposits held with banks may exceed the 
amount of insurance provided on such deposits. Generally these deposits may be redeemed upon demand. 

As of the end of 2014, we had a significant concentration of receivables owed to us by Fujitsu Services Limited, which are 
currently in dispute. Refer to Note (5) for additional information. 

(e) Inventory - Inventory consists primarily of computer hardware and sublicensed software, held for resale. Inventory is 
recorded at the lower of cost (first-in, first-out) or market.

(f) Property and Equipment - We account for property and equipment in accordance with ASC 360, Property, Plant, and 
Equipment. Property, equipment and leasehold improvements are stated at cost. Depreciation of property and equipment is 
computed using the straight-line method over periods of one to 50 years. Amortization of leasehold improvements is computed 
using a straight-line method over the shorter of the lease terms or the useful lives, which range from periods of one to 15 
years. 

(g) Software Development Costs - Software development costs are accounted for in accordance with ASC 985-20, Costs 
of Software to be Sold, Leased or Marketed. Software development costs incurred internally in creating computer software 
products are expensed until technological feasibility has been established upon completion of a detailed program design. 
Thereafter,  all  software  development  costs  incurred  through  the  software’s  general  release  date  are  capitalized  and 
subsequently reported at the lower of amortized cost or net realizable value. Capitalized costs are amortized based on current 
and  expected  future  revenue  for  each  software  solution  with  minimum  annual  amortization  equal  to  the  straight-line 
amortization over the estimated economic life of the solution. We amortize capitalized software development costs over five 
years. 

(h) Goodwill - We account for goodwill under the provisions of ASC 350, Intangibles – Goodwill and Other. Goodwill is not 
amortized but is evaluated for impairment annually or whenever there is an impairment indicator. All goodwill is assigned to 
a reporting unit, where it is subject to an annual impairment assessment.  Based on these evaluations, there was no impairment 
of goodwill in 2014, 2013 or 2012. Refer to Note (7) for more information on goodwill and other intangible assets. 

(i) Derivative Instruments and Hedging Activities - We account for our hedging activities in accordance with ASC 815, 
Derivatives  and  Hedging.  Historically,  our  use  of  hedging  instruments  has  primarily  been  to  hedge  foreign  currency 
denominated assets and liabilities. We record all hedging instruments on our consolidated balance sheets at fair value. For 
hedging instruments that are designated and qualify as a net investment hedge, the effective portion of the gain or loss on 

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the hedging instrument is reported in the foreign currency translation component of other comprehensive income (loss). Any 
ineffective portion of the gain or loss on the hedging instrument is recorded in the results of operations immediately. Refer 
to Note (10) for more information on our hedging activities. 

(j) Income Taxes - Income taxes are accounted for in accordance with ASC 740, Income Taxes. Deferred tax assets and 
liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying 
amounts of existing assets and liabilities and their respective tax bases. Deferred tax assets and liabilities are measured 
using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected 
to be recovered or settled. Refer to Note (13) for additional information regarding income taxes. 

(k) Earnings per Common Share - Basic earnings per share (EPS) excludes dilution and is computed, in accordance with 
ASC 260, Earnings Per Share, by dividing income available to common shareholders by the weighted-average number of 
common shares outstanding for the period. Diluted EPS reflects the potential dilution that could occur if securities or other 
contracts to issue stock were exercised or converted into common stock or resulted in the issuance of common stock that 
then shared in our earnings. Refer to Note (14) for additional details of our earnings per share computations.

(l)  Accounting  for  Share-based  Payments  -  We  recognize  all  share-based  payments  to  associates,  directors  and 
consultants,  including  grants  of  stock  options,  restricted  stock  and  performance  shares,  in  the  financial  statements  as 
compensation  cost  based  on  their  fair  value  on  the  date  of  grant,  in  accordance  with ASC  718,  Compensation-Stock 
Compensation. This compensation cost is recognized over the vesting period on a straight-line basis for the fair value of 
awards that actually vest. Refer to Note (15) for a detailed discussion of share-based payments. 

(m) Foreign Currency - In accordance with ASC 830, Foreign Currency Matters, assets and liabilities of non-U.S. subsidiaries 
whose functional currency is the local currency are translated into U.S. dollars at exchange rates prevailing at the balance 
sheet date. Revenues and expenses are translated at average exchange rates during the year. The net exchange differences 
resulting from these translations are reported in accumulated other comprehensive income. Gains and losses resulting from 
foreign currency transactions are included in the consolidated statements of operations. 

(n) Collaborative Arrangements - In accordance with ASC 808, Collaborative Arrangements, third party costs incurred and 
revenues generated by arrangements involving joint operating activities of two or more parties that are each actively involved 
and exposed to risks and rewards of the activities are classified in the consolidated statements of operations on a gross 
basis only if we are determined to be the principal participant in the arrangement. Otherwise, third party revenues and costs 
generated by collaborative arrangements are presented on a net basis. Payments between participants are recorded and 
classified based on the nature of the payments. 

(o) Recently Issued Accounting Pronouncements

Revenue Recognition. In May 2014, the Financial Accounting Standards Board issued Accounting Standards Update (ASU) 
No. 2014-09, Revenue from Contracts with Customers, which 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.  ASU 2014-09 will replace most existing 
revenue recognition guidance in U.S. GAAP when it becomes effective. This new guidance is effective for the Company in 
the  first  quarter  of  2017,  with  no  early  adoption  permitted.   The  standard  permits  the  use  of  either  the  retrospective  or 
cumulative effect transition method.  At this time we have not selected a transition method.  We are currently evaluating the  
effect that ASU 2014-09 will have on our consolidated financial statements and related disclosures.

(2) Business Acquisitions

Siemens Health Services

On February 2, 2015, we acquired substantially all of the assets, and assumed certain liabilities of Siemens Health Services, 
the health information technology business unit of Siemens AG ("Siemens"), a stock corporation established under the laws 
of Germany.  Siemens Health Services offers a portfolio of enterprise-level clinical and financial health care information 
technology  solutions,  as  well  as  departmental,  connectivity,  population  health,  and  care  coordination  solutions  globally.  
Solutions are offered on the Soarian, Invision, and i.s.h.med platforms, among others.  Siemens Health Services also offers 
a range of complementary and support services including hosting and managed services, implementation services, and 
strategic consulting.

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We believe the acquisition enhances our organic growth opportunities as it provides us a larger base into which we can sell 
our  combined  portfolio  of  solutions  and  services.  The  acquisition  also  augments  our  non-U.S.  footprint  and  growth 
opportunities, increases our ability and scale for R&D investment, and adds approximately 5,500 of highly-skilled associates 
that  will  enhance  our  capabilities.    These  factors,  combined  with  the  synergies  and  economies  of  scale  expected  from 
combining the operations of Cerner and Siemens Health Services, are the basis for acquisition.

Consideration for the acquisition was $1.37 billion of cash, consisting of the $1.3 billion agreed upon price plus working 
capital  adjustments.   The  purchase  price  is  subject  to  certain  post-closing  adjustments  for  working  capital  and  pension 
obligations, as specified in the Master Sale and Purchase Agreement ("MSPA") dated August 5, 2014, as amended.

In 2014 we incurred $15.8 million of pre-tax costs in connection with our acquisition of Siemens Health Services, which are 
included in general and administrative expense in our consolidated statements of operations.

Our acquisition of Siemens Health Services will be treated as a purchase in accordance with ASC 805, Business Combinations, 
which requires allocation of the purchase price to the estimated fair values of assets and liabilities acquired in the transaction.  
Due to the timing of the acquisition subsequent to our 2014 fiscal year-end, certain disclosures, including the preliminary 
allocation of purchase price, have been omitted from this Annual Report on Form 10-K because the initial accounting for the 
business combination is incomplete as of the filing date.  We will include necessary disclosures in our Quarterly Report on 
Form 10-Q for our first fiscal quarter of 2015.

The operating results of Siemens Health Services will be combined with our operating results subsequent to the purchase 
date of February 2, 2015.

InterMedHx

On April 1, 2014, we purchased 100% of the outstanding membership interests of InterMedHx, LLC (InterMedHx). InterMedHx 
is a provider of health technology solutions in the areas of preventive care, patient administration, and medication history. 
We believe the addition of InterMedHx solutions provides additional capabilities in the market. 

Consideration for the acquisition of InterMedHx is expected to total $19.1 million, consisting of up-front cash plus contingent 
consideration, which is payable at a percentage of the revenue contribution from InterMedHx solutions and services.  We 
valued the contingent consideration at $11.6 million based on projections of revenue over the assessment period.

The allocation of purchase price to the estimated fair value of the identified tangible and intangible assets acquired and 
liabilities assumed resulted in goodwill of $16.8 million and $3.8 million in intangible assets related to the value of existing 
technologies. The goodwill was allocated to our Domestic operating segment and is expected to be deductible for tax purposes. 
Identifiable intangible assets are being amortized over a period of five years. 

The operating results of InterMedHx were combined with our operating results subsequent to the purchase date of April 1, 
2014.  Pro-forma results of operations have not been presented because the effect of this acquisition was not material to 
our results. 

PureWellness 

On March 4, 2013, we purchased the net assets of Kaufman & Keen, LLC (doing business as PureWellness).  PureWellness 
is a health and wellness company that develops solutions for the administration and management of wellness programs, 
and to enable plan member engagement strategies.  Our acquisition of PureWellness will further expand what we believe to 
be a robust offering of solutions to manage and improve the health of populations. 

Consideration for the acquisition of PureWellness is expected to total $69.2 million consisting of up-front cash plus contingent 
consideration, which is payable if we achieve certain revenue milestones from PureWellness solutions and services during 
the period commencing on August 1, 2013 and ending April 30, 2015.  We valued the contingent consideration at $19.0 
million based on a probability-weighted assessment of potential contingent consideration payment scenarios.  During 2014, 
we paid $10.6 million to satisfy a portion of this contingent consideration obligation.

The allocation of the purchase price to the estimated fair value of the identified tangible and intangible assets acquired and 
liabilities assumed resulted in goodwill of $48.6 million and $20.3 million in intangible assets, of which $10.5 million and $9.8 
million was related to the value of established customer relationships and existing technologies, respectively.  The goodwill 

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was allocated to our Domestic operating segment and is expected to be deductible for tax purposes. Identifiable intangible 
assets are being amortized over a weighted-average period of seven years.

The operating results of PureWellness were combined with our operating results subsequent to the purchase date of March 4, 
2013. Pro-forma results of operations, assuming this acquisition was made at the beginning of the earliest period presented, 
have not been presented because the effect of this acquisition was not material to our results. 

Labotix 

On March 18, 2013, we purchased 100% of the outstanding stock of Labotix Corporation (together with its wholly owned 
subsidiary Labotix Automation, Inc., Labotix).  Labotix is a developer of laboratory automation solutions for clinical laboratories. 
We believe the combination of Cerner Millennium, Cerner Copath, and Labotix will allow us to offer a comprehensive set of 
capabilities to support high volume laboratory testing. 

Consideration for the acquisition of Labotix was $18.0 million, which was paid in cash. The allocation of purchase price to 
the estimated fair value of the identified tangible and intangible assets acquired and liabilities assumed resulted in goodwill 
of $11.7 million and $5.2 million in intangible assets related to the value of existing technologies. The goodwill was allocated 
to our Domestic operating segment and is not expected to be deductible for tax purposes. Identifiable intangible assets are 
being amortized over a period of five years. 

The operating results of Labotix were combined with our operating results subsequent to the purchase date of March 18, 
2013. Pro-forma results of operations have not been presented because the effect of this acquisition was not material to 
our results.

Anasazi Software, Inc. 

On November 26, 2012, we completed the purchase of 100% of the outstanding stock of Anasazi Software, Inc. (Anasazi). 
Anasazi is a provider of behavioral health technology solutions. We believe the combination of Cerner Millennium, including 
in-patient behavioral health, and Anasazi's community behavioral health solutions create a more comprehensive offering in 
the market. 

Consideration for the acquisition of Anasazi was $47.7 million consisting of up-front cash plus contingent consideration, which 
was payable upon the achievement of certain revenue milestones during 2013 from Anasazi solutions and services.   During 
2013, we paid $0.8 million to satisfy all contingent consideration obligations.

The allocation of the purchase price to the estimated fair value of the identified tangible and intangible assets acquired and 
liabilities assumed resulted in goodwill of $34.6 million and $18.6 million in intangible assets, of which $12.8 million and $5.2 
million was related to the value of established customer relationships and existing technologies, respectively.  The goodwill 
was allocated to our Domestic operating segment and is not expected to be deductible for tax purposes. Identifiable intangible 
assets are being amortized over a weighted-average period of 12 years.

The operating results of Anasazi were combined with our operating results subsequent to the purchase date of November 26, 
2012. 

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(3) Investments

Available-for-sale investments at the end of 2014 were as follows:

(In thousands)

Cash equivalents:

Money market funds

Time deposits

Commercial Paper

Total cash equivalents

Short-term investments:

Time deposits

Commercial paper

Government and corporate bonds

Total short-term investments

Long-term investments:

Government and corporate bonds

Total available-for-sale investments

Available-for-sale investments at the end of 2013 were as follows:

(In thousands)

Cash equivalents:

Money market funds

Time deposits

Commercial Paper

Government and corporate bonds

Total cash equivalents

Short-term investments:

Time deposits

Commercial paper

Government and corporate bonds

Total short-term investments

Long-term investments:

Government and corporate bonds

Total available-for-sale investments

Adjusted
Cost

Gross
Unrealized
Gains

Gross
Unrealized
Losses

Fair Value

$ 189,137

$

— $

— $ 189,137

9,989

115,638

314,764

52,830

435,555

297,311

785,696

219,439

$ 1,319,899

$

—

—

—

—

1

69

70

26

96

—

—

—

(1)

(12)

(90)

(103)

9,989

115,638

314,764

52,829

435,544

297,290

785,663

(500)

218,965

$

(603) $ 1,319,392

Adjusted
Cost

Gross
Unrealized
Gains

Gross
Unrealized
Losses

Fair Value

$

57,254

$

— $

— $

57,254

7,771

3,000

410

68,435

70,303

33,750

572,670

676,723

542,644

—

—

—

—

12

1

356

369

346

—

—

—

—

—

(9)

(79)

(88)

7,771

3,000

410

68,435

70,315

33,742

572,947

677,004

(279)

542,711

$ 1,287,802

$

715

$

(367) $ 1,288,150

Investments reported under the cost method of accounting as of January 3, 2015 and December 28, 2013 were $8.7 million 
and  $7.2  million,  respectively.    Investments  reported  under  the  equity  method  of  accounting  as  of  January 3,  2015  and 
December 28, 2013 were $3.5 million and $5.0 million, respectively.

We sold available-for-sale investments for proceeds of $697.9 million and $125.3 million in 2014 and 2013, respectively, 
resulting in insignificant gains.

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(4) Fair Value Measurements

We determine fair value measurements used in our consolidated financial statements based upon the price that would be 
received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement 
date. The fair value hierarchy distinguishes between (1) market participant assumptions developed based on market data 
obtained  from  independent  sources  (observable  inputs)  and  (2)  an  entity’s  own  assumptions  about  market  participant 
assumptions developed based on the best information available in the circumstances (unobservable inputs). The fair value 
hierarchy consists of three broad levels, which gives the highest priority to unadjusted quoted prices in active markets for 
identical assets or liabilities (Level 1) and the lowest priority to unobservable inputs (Level 3). The three levels of the fair 
value hierarchy are described below: 

• 

• 

• 

Level 1 – Valuations based on quoted prices in active markets for identical assets or liabilities that the entity has the 
ability to access.

Level 2 – Valuations based on quoted prices for similar assets or liabilities, quoted prices in markets that are not 
active, or other inputs that are observable or can be corroborated by observable data for substantially the full term 
of the assets or liabilities.

Level 3 – Valuations based on inputs that are supported by little or no market activity and that are significant to the 
fair value of the assets or liabilities.

The following table details our financial assets measured and recorded at fair value on a recurring basis at the end of 2014: 

(In thousands)

Description

Money market funds

Time deposits

Commercial paper

Time deposits

Commercial paper

Balance Sheet Classification

Cash equivalents

Cash equivalents

Cash equivalents

Short-term investments

Short-term investments

Government and corporate bonds

Short-term investments

Government and corporate bonds

Long-term investments

Fair Value Measurements Using

Level 1

Level 2

Level 3

$ 189,137

$

— $

—
—
—

—

—

—

9,989

115,638

52,829

435,544

297,290

218,965

—

—
—
—

—

—

—

The following table details our financial assets measured and recorded at fair value on a recurring basis at the end of  2013: 

(In thousands)

Description

Money market funds

Time deposits

Commercial paper

Government and corporate bonds

Time deposits

Commercial paper

Balance Sheet Classification

Cash equivalents

Cash equivalents

Cash equivalents

Cash equivalents

Short-term investments

Short-term investments

Government and corporate bonds

Short-term investments

Government and corporate bonds

Long-term investments

Fair Value Measurements Using

Level 1

Level 2

Level 3

$

57,254

$

— $

—

—

—

—

—

—

—

7,771

3,000

410

70,315

33,742

572,947

542,711

—

—

—

—

—

—

—

—

We estimate the fair value of our long-term, fixed rate debt using a Level 3 discounted cash flow analysis based on current 
borrowing rates for debt with similar maturities. The fair value of our long-term debt, including current maturities, at the end 
of 2014 and 2013 was approximately $14.9 million and $32.6 million, respectively. The carrying amount of such fixed-rate 
debt at the end of 2014 and 2013 was $14.2 million and $30.6 million, respectively. 

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(5) Receivables

Receivables  consist  of  accounts  receivable  and  the  current  portion  of  amounts  due  under  sales-type  leases. Accounts 
receivable  represent  recorded  revenues  that  have  been  billed.  Billings  and  other  consideration  received  on  contracts  in 
excess of related revenues recognized are recorded as deferred revenue. Substantially all receivables are derived from sales 
and related support and maintenance and professional services of our clinical, administrative and financial information systems 
and solutions to health care providers located throughout the United States and in certain non-U.S. countries.

We perform ongoing credit evaluations of our clients and generally do not require collateral from our clients. We provide an 
allowance  for  estimated  uncollectible  accounts  based  on  specific  identification,  historical  experience  and  our  judgment. 
Provisions for losses on uncollectible accounts for 2014, 2013, and 2012 totaled $5.3 million, $7.0 million and $13.5 million, 
respectively. 

A summary of net receivables is as follows:

(In thousands)

Gross accounts receivable

Less: Allowance for doubtful accounts

Accounts receivable, net of allowance

Current portion of lease receivables

Total receivables, net

2014

2013

$ 641,160

$ 583,312

25,531

36,286

615,629

547,026

57,149

35,900

$ 672,778

$ 582,926

Lease receivables represent our net investment in sales-type leases resulting from the sale of certain health care devices 
to our clients. The components of our net investment in sales-type leases are as follows:

(In thousands)

Minimum lease payments receivable

Less: Unearned income

Total lease receivables

Less: Long-term receivables included in other assets

Current portion of lease receivables

2014

2013

$ 125,906

$ 146,566

6,089

7,602

119,817

138,964

62,668

103,064

$

57,149

$

35,900

Future minimum lease payments to be received under existing sales-type leases for the next five years are as follows: 

(In thousands)

2015

2016

2017

2018

2019

$

60,198

36,259

20,293

6,986

2,170

During the second quarter of 2008, Fujitsu Services Limited’s (Fujitsu) contract as the prime contractor in the National Health 
Service (NHS) initiative to automate clinical processes and digitize medical records in the Southern region of England was 
terminated by the NHS. This had the effect of automatically terminating our subcontract for the project. We continue to be in 
dispute  with  Fujitsu  regarding  Fujitsu’s  obligation  to  pay  the  amounts  comprised  of  accounts  receivable  and  contracts 
receivable related to that subcontract, and we are working with Fujitsu to resolve these issues based on processes provided 
for  in  the  contract. Part  of  that  process  requires  final  resolution  of  disputes  between  Fujitsu  and  the  NHS  regarding  the 
contract termination. As of January 3, 2015, it remains unlikely that our matter with Fujitsu will be resolved in the next 12 
months. Therefore, these receivables have been classified as long-term and represent less than the majority of other long-
term assets at the end of 2014 and 2013.  While the ultimate collectability of the receivables pursuant to this process is 

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uncertain, we believe that we have valid and equitable grounds for recovery of such amounts and that collection of recorded 
amounts is probable.  Nevertheless, it is reasonably possible that our estimates regarding collectability of such amounts 
might materially change in the near term, considering that we do not have complete knowledge of the status of the proceedings 
between Fujitsu and NHS and their effect on our claim.

During 2014 and 2013, we received total client cash collections of $3.5 billion and $3.1 billion, respectively, of which $79.9 
million and $60.8 million were received from third party arrangements with non-recourse payment assignments.

(6) Property and Equipment

A summary of property, equipment and leasehold improvements stated at cost, less accumulated depreciation and 
amortization, is as follows:

(In thousands)

Computer and communications equipment
Land, buildings and improvements
Leasehold improvements

Furniture and fixtures
Capital lease equipment

Other equipment

Less accumulated depreciation and leasehold amortization

Total property and equipment, net

Depreciable
Lives (Yrs)

1 — 5
12 — 50
1 — 15

5 — 12
3 — 5

3 — 20

2014

2013

$ 1,137,497
439,567
187,351

$ 963,301
411,382
160,030

96,244
3,196

915

72,601
3,207

710

1,864,770

1,611,231

940,510

818,450

$ 924,260

$ 792,781

Depreciation and leasehold amortization expense for 2014, 2013 and 2012 was $163.0 million, $135.7 million and $120.1 
million, respectively. 

(7) Goodwill and Other Intangible Assets

The changes in the carrying amounts of goodwill were as follows: 

(In thousands)

Beginning Balance

Goodwill recorded in connection with business acquisitions

Foreign currency translation adjustment and other

Ending Balance

2014

2013

$ 307,422

$ 247,616

16,757

(3,641)

59,570

236

$ 320,538

$ 307,422

Our intangible assets subject to amortization are amortized on a straight-line basis, and are summarized as follows: 

(In thousands)

Purchased software

Customer lists

Other

Total

Intangible assets, net

2014

2013

Gross
Carrying
Amount

Accumulat
ed
Amortizati
on

Gross
Carrying
Amount

Accumulat
ed
Amortizati
on

$ 169,703

$ 110,344

$ 168,798

$

100,681

68,859

73,637

28,626

100,909

45,915

89,691

68,094

13,705

$ 339,243

$ 212,607

$ 315,622

$ 171,490

$ 126,636

$ 144,132

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Amortization expense for 2014, 2013 and 2012 was $35.9 million, $32.9 million and $20.3 million, respectively. 

Estimated aggregate amortization expense for each of the next five years is as follows: 

(In thousands)

2015

2016

2017

2018

2019

$

34,048

29,359

22,651

8,494

5,208

Note that the above estimate of future amortization expense does not include any impact of intangible assets that may be 
recorded in connection with our February 2, 2015 acquisition of Siemens Health Services, as further described in Note (2).

(8) Software Development

Information regarding our software development costs is included in the following table: 

(In thousands)

Software development costs

Capitalized software development costs

Amortization of capitalized software development costs

Total software development expense

For the Years Ended

2014

2013

2012

$ 467,158 $ 418,747 $ 319,828

(177,800)

(174,649)

(100,189)

103,447

94,688

81,731

$ 392,805 $ 338,786 $ 301,370

Accumulated amortization as of the end of 2014 and 2013 was $890.7 million and $798.0 million, respectively. 

(9) Long-term Debt and Capital Lease Obligations

The following is a summary of indebtedness outstanding:

(In thousands)

Note agreement, 5.54%
Capital lease obligations

Total debt and capital lease obligations
Less: current portion

Long-term debt and capital lease obligations

2014

2013

$

14,233
116,095

$

30,608
135,216

130,328
(67,460)

165,824
(54,107)

$

62,868

$ 111,717

In November 2005, we completed a £65.0 million unsecured private placement of debt at 5.54% pursuant to a Note Agreement. 
The Note Agreement is payable in seven equal annual installments, which commenced November 2009. The proceeds were 
used to repay the outstanding amount under our credit facility and for general corporate purposes. The Note Agreement 
contains certain net worth and fixed charge coverage covenants and provides certain restrictions on our ability to borrow, 
incur liens, sell assets and pay dividends. We were in compliance with all covenants at the end of 2014.

In January 2015, we issued $500.0 million aggregate principal amount of unsecured Senior Notes ("Notes"), pursuant to a 
Master Note Purchase Agreement dated December 4, 2014. The issuance consisted of $225.0 million of 3.18% Series 2015-
A Notes due February 15, 2022, $200.0 million of 3.58% Series 2015-B Notes due February 14, 2025, and $75.0 million in 
floating rate Series 2015-C Notes due February 15, 2022. Interest is payable semiannually on February 15th and August 
15th in each year, commencing on August 15, 2015 for the Series 2015-A Notes and Series 2015-B Notes. The Series 2015-
C Notes will accrue interest at a floating rate equal to the Adjusted LIBOR Rate (as defined in the Master Note Purchase 
Agreement), payable quarterly on February 15th, May 15th, August 15th and November 15th in each year, commencing on 
May 15, 2015. The Master Note Purchase Agreement contains certain leverage and interest coverage ratio covenants and 

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provides certain restrictions on our ability to borrow, incur liens, sell assets, and other customary terms. Proceeds from the 
Notes are available for general corporate purposes.

Our capital lease obligations are primarily related to the procurement of hardware and health care devices, and generally 
have a term of five years. 

Minimum annual payments under existing capital lease obligations and maturities of indebtedness outstanding at the end of 
2014 are as follows:

(In thousands)

2015

2016

2017

2018

2019

Total

Capital Lease Obligations

Minimum
Lease
Payments

Less:
Interest

 Principal

Principal
Amount of
Indebtedn
ess

$

55,968

$

2,741

$

53,227

$

14,233

$

35,968

20,052

6,877

2,137

1,458

530

156

22

34,510

19,522

6,721

2,115

—

—

—

—

 Total

67,460

34,510

19,522

6,721

2,115

$ 121,002

$

4,907

$ 116,095

$

14,233

$ 130,328

We also maintain a $100.0 million multi-year revolving credit facility, which expires in February 2017. The facility provides 
an unsecured revolving line of credit for working capital purposes, along with a letter of credit facility. Interest is payable at 
a rate based on prime, LIBOR, or the U.S. federal funds rate, plus a spread that varies depending on the leverage ratios 
maintained. The agreement provides certain restrictions on our ability to borrow, incur liens, sell assets and pay dividends 
and contains certain cash flow and liquidity covenants.  As of the end of 2014, we were in compliance with all debt covenants. 
As of the end of 2014, we had no outstanding borrowings under this agreement; however, we had $16.6 million of outstanding 
letters of credit, which reduced our available borrowing capacity to $83.4 million. 

(10) Hedging Activities

We designated all of our Great Britain Pound (GBP) denominated long-term debt as a net investment hedge of our U.K. 
operations. The objective of the hedge is to reduce our foreign currency exposure in our U.K. subsidiary investment. Changes 
in the exchange rate between the United States Dollar (USD) and GBP, related to the notional amount of the hedge, are 
recognized as a component of other comprehensive income (loss), to the extent the hedge is effective. The following tables 
represent the fair value of our net investment hedge included within the consolidated balance sheets and the related unrealized 
gain or loss, net of related income tax effects, on the net investment hedge recognized in comprehensive income:  

(In thousands)

Derivatives Designated

Balance Sheet Classification

Total net investment hedge

 Short-term liabilities

(In thousands)

Derivatives Designated

Balance Sheet Classification

Net investment hedge

 Short-term liabilities

Net investment hedge

 Long-term liabilities

Total net investment hedge

62
81

2014

Fair Value

Net
Unrealized
Gain

$

14,233

$

929

2013

Fair Value

Net
Unrealized
Loss

$

$

15,304

$

15,304

30,608

$

178

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(11) Contingencies

We  accrue  estimates  for  resolution  of  any  legal  and  other  contingencies  when  losses  are  probable  and  estimable,  in 
accordance with ASC 450, Contingencies.

The terms of our software license agreements with our clients generally provide for a limited indemnification of such clients 
against losses, expenses and liabilities arising from third party claims based on alleged infringement by our solutions of an 
intellectual property right of such third party. The terms of such indemnification often limit the scope of and remedies for such 
indemnification obligations and generally include a right to replace or modify an infringing solution. To date, we have not had 
to reimburse any of our clients for any losses related to these indemnification provisions pertaining to third party intellectual 
property infringement claims. For several reasons, including the lack of prior indemnification claims and the lack of a monetary 
liability limit for certain infringement cases under the terms of the corresponding agreements with our clients, we cannot 
determine the maximum amount of potential future payments, if any, related to such indemnification provisions.

In addition to commitments and obligations in the ordinary course of business, we are subject to various legal proceedings 
and claims, including for example, employment disputes and litigation alleging solution defects, personal injury, intellectual 
property infringement, violations of law and breaches of contract and warranties.  Many of these proceedings are at preliminary 
stages and many seek an indeterminate amount of damages.

No less than quarterly, we review the status of each significant matter and assess our potential financial exposure. We accrue 
a liability for an estimated loss if the potential loss from any legal proceeding or claim is considered probable and the amount 
can be reasonably estimated. Significant judgment is required in both the determination of probability and the determination 
as to whether the amount of an exposure is reasonably estimable, and accruals are based only on the information available 
to our management at the time the judgment is made. Furthermore, the outcome of legal proceedings is inherently uncertain, 
and we may incur substantial defense costs and expenses defending any of these matters. Should any one or a combination 
of more than one of these proceedings be successful, or should we determine to settle any or a combination of these matters, 
we may be required to pay substantial sums, become subject to the entry of an injunction or be forced to change the manner 
in which we operate our business, which could have a material adverse impact on our financial position or results of operations.

RLIS, Inc., a non-practicing entity, filed a complaint in the Southern District of Texas against the Company alleging that certain 
of the Company’s electronic medical record solutions infringe two patents owned by the plaintiff.  At trial, Plaintiff requested 
damages between $35.3 million and $38.2 million. Plaintiff also sought attorneys’ fees, costs, and an ongoing royalty. A jury 
trial was conducted from January 5, 2015, to January 16, 2015. The jury rendered a verdict that all remaining patent claims 
asserted  against  the  Company  were  invalid  and  not  infringed  by  the  Company. The  Company  continues  to  dispute  the 
Plaintiff’s claims and will vigorously defend itself if the Plaintiff appeals after a final judgment is entered. In the opinion of our 
management, if the Plaintiff were to appeal, there is a reasonable possibility that we could incur losses with respect to this 
matter but we are unable to estimate a range of any such possible losses at this time, and we do not believe a loss is probable.  
Our management will continue to evaluate the potential exposure related to this matter in future periods.

Settlement Charge

On December 10, 2013, the Company received an interim ruling on a pending arbitration matter between Cerner and a 
client, awarding the client damages and awarding us part of our counterclaim to collect accounts receivable.  The client 
dispute arose from allegations that a certain patient accounting software solution sold to the client in 2008 was defective 
and did not deliver the promised benefits.  This matter was resolved and paid in 2013.  We recognized a gross pre-tax 
charge of $106.2 million in the fourth quarter of 2013, which is included in general and administrative expense in our 
consolidated statements of operations.

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(12) Other Income

A summary of other income is as follows:

(In thousands)

Interest income

Interest expense

Other

Other income, net

For the Years Ended
2013

2012

2014

$

16,342

$

15,314

$

16,543

(3,993)

(1,259)

(4,226)

954

(5,068)

4,571

$

11,090

$

12,042

$

16,046

Other income in 2012 includes a $4.5 million gain recognized on the disposition of one of our cost-method investments. 

(13) Income Taxes

Income tax expense (benefit) for 2014, 2013 and 2012 consists of the following: 

(In thousands)

Current:

Federal

State

Foreign

Total current expense

Deferred:

Federal

State

Foreign

Total deferred expense (benefit)

Total income tax expense

For the Years Ended
2013

2012

2014

$ 114,508

$ 178,424

$ 164,690

13,504

13,824

25,148

8,775

13,302

4,142

141,836

212,347

182,134

95,057

8,873

2,975

(9,792)

(7,116)

(5,739)

9,035

4,453

(5,146)

106,905

(22,647)

8,342

$ 248,741

$ 189,700

$ 190,476

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Temporary differences between the financial statement carrying amounts and tax basis of assets and liabilities that give 
rise to significant portions of deferred income taxes at the end of 2014 and 2013 relate to the following: 

(In thousands)

Deferred tax assets:

Accrued expenses

Tax credits and separate return net operating losses

Share based compensation

Contract and service revenues and costs

Other

Gross deferred tax assets

Less: Valuation allowance

Total deferred tax assets

Deferred tax liabilities:

Software development costs
Depreciation and amortization

Contract and service revenues and costs

Other

Total deferred tax liabilities

Net deferred tax liability

2014

2013

$

25,398

$

28,953

58,271

—

10,347

22,948

25,612

44,856

65,407

12,529

122,969

171,352

(776)

(896)

122,193

170,456

(163,938)
(129,684)

(7,511)

(3,625)

(130,583)
(113,492)

—

(2,859)

(304,758)

(246,934)

$ (182,565) $

(76,478)

At the end of 2014, we had net operating loss carry-forwards subject to Section 382 of the Internal Revenue Code for Federal 
income tax purposes of $5.5 million that are available to offset future Federal taxable income, if any, through 2020. We had 
net operating loss carry-forwards from foreign jurisdictions of $0.4 million that are available to offset future taxable income, 
if any, through 2024, $0.7 million that are available to offset future taxable income, if any, through 2033, and $46.8 million 
that are available to offset future taxable income, if any, with no expiration.  We had a deferred tax asset for state net operating 
loss carry-forwards of $0.8 million  which are available to offset future taxable income, if any, through 2034.  In addition, we 
have a state income tax credit carry-forward of $16.0 million available to offset income tax liabilities through 2030.

During 2013, we recorded a valuation allowance of $0.9 million against our deferred tax asset for certain foreign net operating 
losses, generated in prior years, because we concluded that it is not more likely than not that we will generate income of the 
appropriate character to utilize these losses.  We expect to fully utilize all the remaining net operating loss and tax credit 
carry-forwards in future periods.

At  the  end  of  2014,  we  had  not  provided  tax  on  the  cumulative  undistributed  earnings  of  our  foreign  subsidiaries  of 
approximately $99 million, because it is our intention to reinvest these earnings indefinitely. If these earnings were distributed, 
we would be subject to U.S. taxes and foreign withholding taxes, net of U.S. foreign tax credits which may be available. The 
calculation of this unrecognized deferred tax liability is complex and not practicable. 

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The effective income tax rates for 2014, 2013, and 2012 were 32%, 32%, and 32%, respectively. These effective rates differ 
from the Federal statutory rate of 35% as follows: 

(In thousands)

Tax expense at statutory rates

State income tax, net of federal benefit

Tax credits

Unrecognized tax benefit (including interest)

Permanent differences

Other, net

Total income tax expense

For the Years Ended

2014

2013

2012

$ 270,961

$ 205,819

$ 205,698

15,715

(20,986)

5,538

(12,253)

(10,234)

17,502

(18,683)

(20)

(14,760)

(158)

13,856

(1,510)

(12,832)

(19,900)

5,164

$ 248,741

$ 189,700

$ 190,476

 A reconciliation of the beginning and ending amount of unrecognized tax benefit is presented below:

(In thousands)

Unrecognized tax benefit - beginning balance

Gross decreases - tax positions in prior periods

Gross increases - tax positions in prior periods

Unrecognized tax benefit - ending balance

2014

2013

2012

$

$

2,100

$

2,176

$

14,640

(804)

5,906

(76)

—

(12,464)

—

7,202

$

2,100

$

2,176

If recognized, $5.9 million of the unrecognized tax benefit will favorably impact our effective tax rate. We anticipate that it is 
reasonably possible that our unrecognized tax benefits will decrease by up to $4 million within the next twelve months due 
to the potential settlement of examinations and lapse of the statutes of limitations in various taxing jurisdictions.  Our federal 
returns have been examined by the Internal Revenue Service through 2009.  Our federal returns for 2010 through 2012 are 
currently under examination by the Internal Revenue Service.  We have various state and foreign returns under examination.  

The 2014 beginning and ending amounts of accrued interest related to unrecognized tax benefits were $0.2 million and $0.6 
million, respectively. We classify interest and penalties as income tax expense in our consolidated statement of operations. 
No accrual for tax penalties was recorded at the end of the year.

The foreign portion of our earnings before income taxes was $68.3 million, $4.5 million, and ($15.4) million in 2014, 2013, 
and 2012 respectively, and the remaining portion was domestic.

(14) Earnings Per Share

A reconciliation of the numerators and the denominators of the basic and diluted per share computations are as follows:

2014

2013

2012

Earnings

Shares

Per-
Share

Earnings

Shares

Per-
Share

Earnings

Shares

Per-
Share

(In thousands, except per share data)

(Numerator)

(Denominator)

Amount

(Numerator)

(Denominator)

Amount

(Numerator)

(Denominator)

Amount

Basic earnings per share:

Income available to common shareholders

$

525,433

342,150

$

1.54

$

398,354

343,636

$

1.16

$

397,232

341,861

$

1.16

Effect of dilutive securities:

Stock options and non-vested shares

—

8,236

—

8,645

—

9,533

Diluted earnings per share:

Income available to common shareholders

including assumed conversions

$

525,433

350,386

$

1.50

$

398,354

352,281

$

1.13

$

397,232

351,394

$

1.13

Options to purchase 5.7 million, 6.1 million and 4.6 million shares of common stock at per share prices ranging from $44.05 
to $66.10, $36.92 to $56.39 and $27.62 to $42.98, were outstanding at the end of 2014, 2013 and 2012, respectively, but 
were not included in the computation of diluted earnings per share because they were anti-dilutive. 

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(15) Share-Based Compensation and Equity

Stock Option and Equity Plans

As of the end of 2014, we had five fixed stock option and equity plans in effect for associates and directors. This includes 
one plan from which we could issue grants, the Cerner Corporation 2011 Omnibus Equity Incentive Plan (the Omnibus Plan); 
and four plans from which no new grants are permitted, but some awards remain outstanding (Plans D, E, F, and G). 

Awards under the Omnibus Plan may consist of stock options, stock appreciation rights, restricted stock, restricted stock 
units, performance shares, performance units, performance grants and bonus shares. At the end of 2014, 8.1 million shares 
remain available for awards. Stock options granted under the Omnibus Plan are exercisable at a price not less than fair 
market value on the date of grant. Stock options under the Omnibus Plan typically vest over a period of five years and are 
exercisable for periods of up to 10 years. 

Stock Options 

The fair market value of each stock option award is estimated on the date of grant using a lattice option-pricing model. The 
pricing model requires the use of the following estimates and assumptions: 

•  Expected volatilities under the lattice model are based on an equal weighting of implied volatilities from traded options 
on our shares and historical volatility. We use historical data to estimate the stock option exercise and associate 
departure behavior used in the lattice model; groups of associates (executives and non-executives) that have similar 
historical behavior are considered separately for valuation purposes.

•  The expected term of stock options granted is derived from the output of the lattice model and represents the period 

of time that stock options granted are expected to be outstanding. 

•  The risk-free rate is based on the zero-coupon U.S. Treasury bond with a term equal to the contractual term of the 

awards. 

The weighted-average assumptions used to estimate the fair market value of stock options are as follows: 

Expected volatility (%)
Expected term (yrs)
Risk-free rate (%)

Stock option activity for 2014 was as follows:

(In thousands, except per share data)
Outstanding at beginning of year
Granted
Exercised
Forfeited and expired
Outstanding at end of year

Exercisable at end of year

2014

2013

2012

29.7%
9.1
2.9%

30.5%
9.1
1.9%

34.8%
9.1
2.1%

Weighted-
Average
Exercise 
Price

Aggregate
Intrinsic 
Value

Number of
Shares

Weighted-
Average      
Remaining      
Contractual
 Term (Yrs)      

$

24,407
3,271
(2,719)
(330)
24,629

22.24
52.19
12.70
42.31
27.00

$ 936,584

14,387

$

14.39

$ 728,611

6.00

4.50

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(In thousands, except for grant date fair values)

Weighted-average grant date fair values

Total intrinsic value of options exercised

Cash received from exercise of stock options

Tax benefit realized upon exercise of stock options

For the Years Ended

2014

2013

2012

$

22.59

$

19.57

$

18.52

$ 124,828

$ 118,051

$ 152,117

31,879

44,029

31,403

43,523

38,147

55,952

As of the end of 2014, there was $136.1 million of total unrecognized compensation cost related to stock options granted 
under all plans. That cost is expected to be recognized over a weighted-average period of 3.10 years.

Non-vested Shares

Non-vested shares are valued at fair market value on the date of grant and will vest provided the recipient has continuously 
served  on  the  Board  of  Directors  through  such  vesting  date  or,  in  the  case  of  an  associate,  provided  that  performance 
measures are attained. The expense associated with these grants is recognized over the period from the date of grant to 
the vesting date, when achievement of the performance condition is deemed probable. 

Non-vested share activity for 2014 was as follows: 

(In thousands, except per share data)

Outstanding at beginning of year
Granted
Vested
Forfeited

Outstanding at end of year

(In thousands, except for grant date fair values)

Weighted average grant date fair values for shares granted during the year

Total fair value of shares vested during the year

Weighted-
Average
Grant Date 
Fair Value

Number of 
Shares

$

552
167
(208)
(5)

506

$

38.54
55.27
33.38
34.48

46.21

For the Years Ended

2014

2013

2012

$

$

55.27

11,294

$

$

46.66

13,649

$

$

38.28

2,612

As of the end of 2014, there was $11.0 million of total unrecognized compensation cost related to non-vested share awards 
granted under all plans. That cost is expected to be recognized over a weighted-average period of 1.29 years.

Associate Stock Purchase Plan 

We established an Associate Stock Purchase Plan (ASPP) in 2001, which qualifies under Section 423 of the Internal Revenue 
Code. Each individual employed by us and associates of our United States based subsidiaries, except as provided below, 
are eligible to participate in the ASPP (Participants). The following individuals are excluded from participation: (a) persons 
who, as of the beginning of a purchase period under the Plan, have been continuously employed by us or our domestic 
subsidiaries for less than two weeks; (b) persons who, as of the beginning of a purchase period, own directly or indirectly, 
or hold options or rights to acquire under any agreement or Company plan, an aggregate of 5% or more of the total combined 
voting power or value of all outstanding shares of all classes of Company Common Stock; and, (c) persons who are customarily 
employed by us for less than 20 hours per week or for less than five months in any calendar year. Participants may elect to 
make contributions from 1% to 20% of compensation to the ASPP, subject to annual limitations determined by the Internal 
Revenue Service. Participants may purchase Company Common Stock at a 15% discount on the last business day of the 
option period. The purchase of Company Common Stock is made through the ASPP on the open market and subsequently 
reissued to Participants. The difference between the open market purchase and the Participant’s purchase price is recognized 
as compensation expense, as such difference is paid by Cerner, in cash.

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Share Based Compensation Cost

Our stock option and non-vested share awards qualify for equity classification. The costs of our ASPP, along with participant 
contributions,  are  recorded  as  a  liability  until  open  market  purchases  are  completed.  The  amounts  recognized  in  the 
consolidated statements of operations with respect to stock options, non-vested shares and ASPP are as follows: 

(In thousands)

Stock option and non-vested share compensation expense

Associate stock purchase plan expense

Amounts capitalized in software development costs, net of amortization

Amounts charged against earnings, before income tax benefit

Amount of related income tax benefit recognized in earnings

Preferred Stock

For the Years Ended

2014

2013

2012

$

59,292

$

46,295

$

36,113

4,603

(930)

3,704

(1,045)

2,859

(860)

$

$

62,965

22,101

$

$

48,954

18,607

$

$

38,112

14,578

As of the end of 2014 and 2013, we had 1.0 million shares of authorized but unissued preferred stock, $0.01 par value.

Treasury Stock

In  May  2014,  our  Board  of  Directors  approved  an  amendment  to  the  stock  repurchase  program  that  was  authorized  in 
December 2013.  Under the amendment, the Company may repurchase shares of our common stock up to an additional 
$100.0 million.  This increase authorizes repurchases of up to $317.0 million, in the aggregate, excluding transaction costs.  
The repurchases are to be effectuated in the open market, by block purchase, or possibly through other transactions managed 
by broker-dealers. No time limit was set for completion of the program.

During 2014, we repurchased 4.1 million shares for consideration of $217.0 million, excluding transaction costs.  These 
shares were recorded as treasury stock and accounted for under the cost method.  No repurchased shares have been retired.  
At January 3, 2015, $100.0 million remains available for purchases under the program.

In December 2012, our Board of Directors authorized a stock repurchase program of up to $170.0 million, excluding transaction 
costs, of our common stock.  During 2013, we repurchased 3.6 million shares for total consideration of $170.0 million. All of 
the repurchased shares at the time of our June 2013 stock split were utilized to settle a portion of the stock split distribution. 
This program is now complete.

(16) Foundations Retirement Plan

The Cerner Corporation Foundations Retirement Plan (the Plan) was established under Section 401(k) of the Internal Revenue 
Code. All associates age 18 and older and who are not a member of an excluded class are eligible to participate. Participants 
may elect to make pretax contributions from 1% to 80% of eligible compensation to the Plan, subject to annual limitations 
determined by the Internal Revenue Service. Participants may direct contributions into mutual funds, a stable value fund, a 
Company stock fund, or a self-directed brokerage account. The Plan has a first tier discretionary match that is made on 
behalf of participants in an amount equal to 33% of the first 6% of the participant’s salary contribution.  The Plan's first tier 
discretionary match expenses amounted to $17.9 million, $14.9 million and $12.3 million for 2014, 2013 and 2012, respectively. 

We  added  a  second  tier  discretionary  match  to  the  Plan  in  2000.  Contributions  are  based  on  attainment  of  established 
earnings per share goals for the year or the established financial metric for the Plan. Participants who defer 2% of their paid 
base salary, are actively employed as of the last day of the Plan year and are employed before October 1st of the Plan year 
are eligible to receive the second tier discretionary match contribution. For the years ended 2014, 2013 and 2012 we expensed 
$4.9 million, $13.5 million and $11.9 million for the second tier discretionary distributions, respectively. 

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(17) Related Party Transactions

Continuous Campus

During 2009, as part of our long-term space planning analysis, we determined that we would require additional office space 
for associates to accommodate our anticipated growth. We evaluated various sites in the Kansas City metropolitan area and 
negotiated with several different governmental entities regarding available incentives. Upon completion of this review, we 
decided to proceed with an office development (known as our “Continuous Campus”) in Wyandotte County, Kansas. In order 
to maximize available incentives, we agreed to pursue the office development in conjunction with the development of an 
18,000 seat, multi-sport stadium complex and related recreational athletic complex.

The stadium complex was developed by Kansas Unified Development, LLC (the “Developer”), an entity controlled by Neal 
Patterson, Chairman of the Board of Directors and Chief Executive Officer of the Company, and Clifford Illig, Vice Chairman 
of the Board of Directors of the Company. Sporting Kansas City (“Sporting KC”) is the principal tenant of the stadium complex. 
OnGoal LLC (“OnGoal”), the owner of the Sporting KC professional soccer club, is also controlled by Messrs. Patterson and 
Illig.

The Company currently estimates it will receive incentives in the aggregate of $82.0 million from the Developer, the Unified 
Government  of  Wyandotte  County/Kansas  City,  Kansas  (the  “Unified  Government”)  and  the  Kansas  Department  of 
Commerce.  Components of the $82.0 million of incentives are described below:

Cash Grants - In January 2014 we received $48.0 million of cash grants from the Kansas Department of Commerce for 
project costs.  The State of Kansas has issued bonds in order to fund these incentives and has incurred costs of issuance 
and  debt  service  obligations. As  consideration  for  the  grant,  we  made  certain  new  job  and  state  payroll  tax  withholding 
commitments.  Should aggregate state payroll tax withholdings (related to associates at our Continuous Campus) over a 10-
year period commencing in January 2014 be less than $51.9 million (the $48.0 million of cash we received plus amounts 
representing debt service costs incurred by the State of Kansas), we would be required to repay the shortfall.  The $51.9 
million maximum repayment amount will be adjusted up or down during the 10-year period, based on any future change to 
Kansas payroll tax withholding rates. 

Under a separate agreement, the Developer and OnGoal have agreed to be responsible for certain shortfall payments that 
may become due.  If no payment from Developer or OnGoal becomes due at the end of the 10-year period, the Developer 
or OnGoal will pay us a success fee of $4.0 million.

We recorded the cash grants as an obligation/liability at $48.0 million, upon receipt in January 2014.  Over time this liability 
will accrete, utilizing the effective interest method, up to the maximum repayment amount, offset by reductions based on 
actual  state  payroll  tax  withholdings  generated  by  our  Continuous  Campus  associates.   This  activity  is  recognized  as  a 
component of operating expense as it occurs over a period not to exceed 10 years.  At the end of 2014, the obligation/liability 
balance was $43.0 million, the majority of which is included in deferred income taxes and other liabilities in our consolidated 
balance sheets.

Sales Tax Exemptions - We have received a sales tax exemption on materials and other fixed assets purchased in connection 
with the construction.  As such, we will not be required to remit an aggregate of $11.5 million of sales tax on these capital 
purchases.

State Income Tax Credits - We expect state income tax credits to aggregate $18.5 million.  Such credits are available to 
offset our Kansas state income tax in the future, and will be recognized as a reduction of income tax expense as we are 
eligible to claim them.

Land - We acquired the land for our Continuous Campus from the Unified Government with certain contingencies upon which 
the office complex was being constructed. The purchase price of the land, equal to the site’s fair market value, is being paid 
by the Developer. In the second quarter of 2012, we commenced vertical construction on the office development, which 
resolved contingencies and the land contributed to the Company from the Unified Government was recorded at its $4.0 
million appraisal value.

In 2012, we contracted with GRAND Construction, LLC (“Grand”), a limited liability company owned in part by an entity 
controlled by Messrs. Patterson and Illig, to coordinate, supervise, schedule and assist with managing the development, 

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design and construction of our Continuous Campus. Under the agreement, we paid Grand $0.4 million, $1.4 million, and 
$1.4 million in 2014, 2013, and 2012, respectively.  This contract was completed in 2014.

We also paid Grand $0.3 million in both 2013 and 2012 for separate projects to make improvements to parking facilities 
utilized by one of our other office campuses.

Trails Campus Development

In December 2013, we purchased approximately 237 acres of land located in Kansas City, Missouri, from Trails Properties 
II, Inc. (“Trails”), for $42.5 million. Trails is an entity controlled by Messrs. Patterson and Illig.  The property (currently known 
as our "Trails Campus") was acquired as a site for future office space development to further accommodate our anticipated 
growth.  Construction on the Trails Campus began in November 2014.

In December 2014, we contracted with Grand to coordinate, supervise, schedule and assist with managing the development, 
design and construction of the first two phases of our Trails Campus.  Under the agreement, we expect to pay Grand $3.6 
million over a period estimated at two years.

(18) Commitments

Leases 

We are committed under operating leases primarily for office and data center space and computer equipment through October 
2027. Rent expense for office and warehouse space for our regional and global offices for 2014, 2013 and 2012 was $25.1 
million,  $20.0  million  and  $18.1  million,  respectively. Aggregate  minimum  future  payments  under  these  non-cancelable 
operating leases are as follows: 

(In thousands)

2015

2016

2017

2018

2019

2020 and thereafter

Operating
Lease
Obligations

$

23,525

21,693

21,467

19,294

14,984

39,607

$

140,570

Other Obligations 

We have purchase commitments with various vendors, and minimum funding commitments under collaboration agreements 
through 2023. Aggregate future payments under these commitments are as follows: 

(In thousands)

2015
2016
2017
2018
2019
2020 and thereafter

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90

Purchase
Obligations

$

42,300
23,481
6,762
4,345
4,001
8,000

$

88,889

 
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Siemens Innovation Alliance

Concurrently with the execution of the MSPA, we entered into an agreement with Siemens to create a strategic alliance to 
jointly invest in innovative projects that integrate health information technology with medical technologies for the purpose of 
enhancing workflows and improving clinical outcomes.  Each company will contribute up to $50.0 million to fund projects of 
shared importance to both companies and their clients, over an initial term of three years, commencing on February 2, 2015.

(19) Segment Reporting

We have two operating segments, Domestic and Global. Our Chief Executive Officer is our chief operating decision maker 
("CODM"). Revenues are derived primarily from the sale of clinical, financial and administrative information systems and 
solutions.  The  cost  of  revenues  includes  the  cost  of  third  party  consulting  services,  computer  hardware,  devices  and 
sublicensed software purchased from manufacturers for delivery to clients. It also includes the cost of hardware maintenance 
and  sublicensed  software  support  subcontracted  to  the  manufacturers.  Operating  expenses  incurred  by  the  geographic 
business segments consist of sales and client service expenses including salaries of sales and client service personnel, 
communications expenses and unreimbursed travel expenses. “Other” includes expenses that have not been allocated to 
the operating segments, such as software development, marketing, general and administrative (including the settlement 
charge discussed in Note (11)), acquisition costs, share-based compensation expense and depreciation. Performance of the 
segments is assessed at the operating earnings level and, therefore, the segment operations have been presented as such, 
as  our  CODM  reviews  segment  performance  exclusive  of  these  charges.  Items  such  as  interest,  income  taxes,  capital 
expenditures and total assets are managed at the consolidated level and thus are not included in our operating segment 
disclosures. Accounting policies for each of the reportable segments are the same as those used on a consolidated basis. 

The following table presents a summary of our operating segments and other expense for 2014, 2013 and 2012:

(In thousands)

2014

Revenues

Cost of revenues
Operating expenses

Total costs and expenses

Operating earnings (loss)

(In thousands)

2013

Revenues

Cost of revenues

Operating expenses

Total costs and expenses

Operating earnings (loss)

(In thousands)

2012

Revenues

Cost of revenues

Operating expenses

Total costs and expenses

Operating earnings (loss)

Domestic

Global    

Other    

Total    

$ 3,021,790

$ 380,913

$

— $ 3,402,703

542,210
677,817
1,220,027

62,167
131,096
193,263

—
1,226,329
1,226,329

604,377
2,035,242
2,639,619

$ 1,801,763

$ 187,650

$(1,226,329) $ 763,084

Domestic

Global    

Other    

Total    

$ 2,550,115

$ 360,633

$

— $ 2,910,748

458,540

600,341

1,058,881

56,182

115,281

171,463

—

514,722

1,104,392

1,820,014

1,104,392

2,334,736

$ 1,491,234

$ 189,170

$(1,104,392) $ 576,012

Domestic

Global    

Other    

Total    

$ 2,341,304

$ 324,132

$

— $ 2,665,436

548,813

506,249

1,055,062

59,384

131,580

190,964

—

608,197

847,748

847,748

1,485,577

2,093,774

$ 1,286,242

$ 133,168

$ (847,748) $ 571,662

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(20) Quarterly Results (unaudited)

Selected quarterly financial data for 2014 and 2013 is set forth below: 

(In thousands, except per share data)

2014 quarterly results:

First Quarter

Second Quarter

Third Quarter (a)

Fourth Quarter (a)

Total

Earnings
Before
Income
Taxes

Revenues

Net
Earnings

Basic
Earnings
Per Share

Diluted
Earnings
Per Share

$ 784,761

$ 180,993

$ 119,526

$

0.35

$

851,762

194,370

129,033

840,149

190,335

129,002

926,031

208,476

147,872

0.38

0.38

0.43

$ 3,402,703

$ 774,174

$ 525,433

0.34

0.37

0.37

0.42

(a) Third and Fourth quarter results include pre-tax acquisition costs of $9.4 million and $6.4 million, respectively, as further described in Note (2).

(In thousands, except per share data)

2013 quarterly results:

First Quarter

Second Quarter

Third Quarter

Fourth Quarter (b)

Total

Earnings
Before
Income
Taxes

Revenues

Net
Earnings

Basic
Earnings
Per Share

Diluted
Earnings
Per Share

$ 680,029

$ 159,613

$ 110,040

$

0.32

$

707,561

169,189

112,907

727,830

172,747

115,344

795,328

86,505

60,063

0.33

0.34

0.17

$ 2,910,748

$ 588,054

$ 398,354

0.31

0.32

0.33

0.17

(b) Fourth quarter results include a pre-tax settlement charge of $106.2 million, as further described in Note (11).

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STOCK PRICE PERFORMANCE GRAPH

The following graph presents a comparison for the five-year period ended December 31, 2014 of the 
performance of the Common Stock of the Company with the NASDAQ Composite Index (U.S.Companies) 
(as calculated by The Center for Research in Security Prices), the NASDAQ Computer and Data Processing 
Index (as calculated by The Center for Research in Security Prices), the ICB: 9533 Computer Services 
(Subsector) Index and the NASDAQ US Benchmark TR Index. As a result of a change in the total return 
data made available to us through our third-party index provider, in lieu of using indices calculated by 
the Center for Research in Security Prices, as we have in prior years, our performance graphs going 
forward  will  be  using  comparable  indices  provided  by  NASDAQ  OMX  Global  Indexes.  Please  note, 
information for the NASDAQ Computer and Data Processing Index and the NASDAQ Composite Index 
(U.S. Companies) is provided only from December 31, 2009 through December 31, 2013, the last day 
this data was available by our third-party index provider. These indices have been replaced by the ICB: 
9533 Computer Services (Subsector) Index and NASDAQ U.S. Benchmark TR Index, respectively.

Comparison of 5-Year Cumulative Total Return

$350

$300

$250

$200

$150

$100

$50

$0

12/09

12/10

12/11

12/12

12/13

12/14

Cerner Corporation

NASDAQ Computer and Data Processing Index

NASDAQ Stock Market (U.S. Companies)

ICB: 9533 Computer Services (Subsector)

NASDAQ U.S. Benchmark TR Index

The above comparison assumes $100 was invested on December 31, 2009 in Common Stock of the 
Company  and  in  each  of  the  foregoing  indices  and  assumes  reinvestment  of  dividends.  The  results 
of  each  component  issuer  of  each  group  are  weighted  according  to  such  issuer’s  stock  market 
capitalization at the beginning of each year.

93

Corporate Information

ANNUAL SHAREHOLDERS’ MEETING

The Annual Shareholders’ Meeting will be held at 10:00 a.m. local time on May 22, 2015, in The Cerner 
Round  Auditorium  in  the  Cerner  Vision  Center,  located  on  the  Cerner  campus  at  2850  Rockcreek 
Parkway, North Kansas City, Missouri, 64117. A formal notice of the Meeting, with a Proxy Statement 
and Proxy Card, will be available to each shareholder of record in April 2015.

ANNUAL REPORT/FORM 10-K

Publications of interest to current and potential Cerner investors are available upon written request or 
via Cerner’s Web site at www.cerner.com. These include annual and quarterly reports and the Form 
10-K filed with the Securities and Exchange Commission.

Written requests should be made to:

Cerner Corporation 
Investor Relations 
2800 Rockcreek Parkway 
North Kansas City, MO 64117-2551

Inquiries of an administrative nature relating to shareholder accounting records, stock transfer, change 
of  address  and  miscellaneous  shareholder  requests  should  be  directed  to  the  transfer  agent  and 
registrar, Computershare Trust Company, at 1-800-884-4225.

TRANSFER AGENT AND REGISTRAR

Computershare Trust Company, N.A. 
P.O. Box 43078 
Providence, RI 02940-3078 
1-800-884-4225

STOCK LISTINGS

Cerner Corporation’s common stock trades on The NASDAQ Stock Market under the symbol CERN.

INDEPENDENT ACCOUNTANTS

KPMG LLP 
Kansas City, MO

Cerner connects people and systems through our open, powerful and versatile platforms 
and solutions, providing information where it’s needed most. Together with 
our clients and industry collaborators, we’re creating a future where the health system 
works to improve the well-being of individual people and entire populations.

94

© Cerner Corporation. All Rights Reserved. All Cerner trademarks and logos are owned or licensed by Cerner Corporation 

and/or its affiliates. All other brand or product names are trademarks or registered marks of their respective owners.

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Cerner connects people and systems through our open, powerful and versatile platforms 

and solutions, providing information where it’s needed most. Together with 

our clients and industry collaborators, we’re creating a future where the health system 

works to improve the well-being of individual people and entire populations.

© Cerner Corporation. All Rights Reserved. All Cerner trademarks and logos are owned or licensed by Cerner Corporation 
and/or its affiliates. All other brand or product names are trademarks or registered marks of their respective owners.

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Connecting what mattersTM

World Headquarters
Cerner Corporation
2800 Rockcreek Parkway
Kansas City, MO USA 64117
816 201 1024

Worldwide
Australia
Austria
Belgium
Brazil
Canada
Chile
Egypt
Finland
France
Germany
India
Ireland
Malaysia

Mexico
Netherlands
Norway
Portugal
Qatar
Romania
Saudi Arabia
Singapore
Slovakia
Spain
Sweden
United Arab Emirates
United Kingdom

Health care is too important to stay the same.TM
cerner.com

Cerner Corporation      2014 Annual Report

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