News, Analysis, Trends, Management Innovations for
Clinical Laboratories and Pathology Groups

Hosted by Robert Michel

News, Analysis, Trends, Management Innovations for
Clinical Laboratories and Pathology Groups

Hosted by Robert Michel
Sign In

PAMA in 2019: What Labs Need to Know
to Collect Data, Report on Time
and Avoid $10,000 per day Penalties

 

Webinar held February 20, 2019

Please contact us at 512-26-7103 or info@darkreport.com for information

Recent changes made to PAMA regulations in the last few months mean that many more hospital and other labs must now report their PAMA private payer price data to Medicare. These revisions to reporting requirements and fees will dramatically affect all laboratories!

In fact, your laboratory or organization faces considerable risk if not compliant with the latest PAMA requirements, with continuing adjustments and proposals to the Clinical Laboratory Fee Schedule carrying far-reaching budget implications. The most current understanding of PAMA’s impact is crucial!

This 90-minute program, including an interactive Q&A session, is a must-attend event for everyone in your hospital and lab team responsible for gathering, analyzing, and reporting data to CMS. You’ll get answers to your toughest questions and master the knowledge you need to report accurate and complete data on time!

Learn about how the current PAMA rules will affect your laboratory operationally, the magnitude of PAMA’s financial impact to your organization, members of your team crucial to include in the data collection and reporting process, the latest on very recent changes regarding hospital outreach programs, and much more!

Attend this program, and our experts will guide you through the following important areas

•  Who has to report this year and why reporting requirements changed

•  Collection and reporting periods under current PAMA rules

•  The definition of “applicable information” when reporting and how to establish appropriate reporting capabilities

•  Why proper data capture is critical, data validation, and preparing for data submission

•  Assessing your billing and IT limitations and responding accordingly

•  Up-to-the-minute info on potential issues specific to hospital outreach programs

•  Strategies to offset PAMA impact in your laboratory, compliance obstacles that you may encounter, and much more!

Who should attend?

•  Laboratory Directors, Managers, and Administrators

•  Hospital COOs, CFOs, CIOs, Contract Officers, Compliance Officers

•  Laboratory IT and Billing Departments

Please contact us at 512-26-7103 or info@darkreport.com for information


Our expert speakers:

Rodney W. Forsman
Assistant Professor Emeritus, Lab Medicine and Pathology
College of Medicine
Mayo Clinic
Rochester, MN

Brian Kemp
Vice President
Change Healthcare
North Charleston, SC

Your order includes:

•  A site license to attend the webinar. Invite as many members of your team as you would like!

•  A full transcript emailed to you soon after the conference

For more information, call us at 512-264-7103.


Speakers:

Stephen Stone

Rodney W. Forsman
Assistant Professor Emeritus, Lab Medicine and Pathology
College of Medicine
Mayo Clinic
Rochester, MN

Over the past ten years, Rod has been a President, Secretary/Treasurer and a Director of the Clinical Laboratory Management Association (CLMA). He is currently on the Board of Directors for Path-Tec. He is a member of the American College of Healthcare Executives (ACHE), the American Association for Clinical Chemistry (AACC), the CLMA Legislative Compliance and Regulatory Committee (LCRC) and the CLMA Finance Committee.

Spanning the past five decades, Rod was a member of the Department of Laboratory Medicine and Pathology at Mayo Clinic in Rochester as a development technologist, Supervisor, Coordinator of purchasing, Coordinator of quality assurance, Administrative Director of sales for Mayo Medical Laboratories (MML) and President of MML New England.  He participated in the expansion of the Mayo laboratory practice from a local outreach program to one serving thousands of hospitals worldwide. 

Rod has actively participated in laboratory advocacy efforts together with the Clinical Laboratory Coalition, the CLMA and the AACC. He has been a member of the AMA Molecular Pathology CPT coding workgroup, the Mayo Public Affairs-Federal committee and the AACC Government Relations Committee. He also coordinated licensure, accreditation and legislative affairs for the laboratories at Mayo Clinic.

Rita D’Angelo

Brian Kemp
Vice President
Change Healthcare
North Charleston, SC

The Vice President of Laboratory Operations and Client Management for Change Healthcare’s Technology Enabled Services, Brian Kemp has over 25 years of experience in financial management and business operations. In 2008, he joined Change Healthcare as Director of Client Management supporting the laboratory business. In his tenure with Change Healthcare, Kemp has directed the client management aspects of both the pathology and laboratory businesses.

Immediately before joining Change Healthcare, Kemp held the position of Director of Finance at Bostwick Laboratories. Prior to that, he built a strong track record of industry experience in retail, insurance, and financial services.

Kemp holds a Bachelor of Business Administration degree in accounting from the College of William and Mary, a Master of Business Administration degree in marketing and operations from Indiana University, and an expired CPA license in the commonwealth of Virginia.

;