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Webinar | Medicare Coverage and Clinical Trials

Description

Essential Components of a Clinical Trial Agreement | Webinar Series

Historically, when payors saw that patients were enrolled in clinical trials, they declined to cover many routine costs of care and presumed many costs were associated with the clinical trial. This led to many sponsors excluding older participants who may have a variety of medical conditions. To encourage device and drug manufacturers to include Medicare beneficiaries in clinical trials, a law was passed wherein Medicare (and Medicare Advantage Organizations), would cover not only routine costs that would have been covered absent a clinical trial, but would also cover a portion of the costs of the clinical trial and medical complications that might arise from such participation. In this webinar, we will learn how savvy sponsors and institutions conduct analyses of the costs of a clinical trial and bill Medicare for medical services when possible.

Learning Objectives:

  1. How to qualify a clinical trial for Medicare coverage of certain costs.
  2. How to minimize the chances that clinical trial costs will prompt an audit of a facility's billing practices.
Knowledge Level: All Levels

Registration
(Deadline May 15)
Late Registration***
(After May 15)

Individual Registration
Member Rate* $99 $114
Non-Member Rate $165 $180
Group Registration**
Member/Non-Member Rate $350 $365

Register for the entire Webinar Series for one low rate!

Registration includes access to the live event, PowerPoint slides, and complimentary access to the On-Demand version for 30-days.
*To receive the member registration rate, you must an SRAI member during the event.
**All Group Attendees must be added when registering. Up to 12 attendees per group.
***If registering late, please contact registration@srainternational.org for assistance.

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  • Click the blue Register button to register for the Webinar
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Policies:
Written requests for registration refunds must be postmarked on or before May 9. Cancellations submitted on or before May 9, less a $25 meeting cancellation fee. If you paid membership dues while registering, these will not be refunded; only the actual registration fees will be refunded less the cancellation fee(s). No refunds will be made after May 9. Refunds are not given for no-shows. Registration substitutions from the same institution are accepted; membership substitutions are NOT accepted. All fees will be reimbursed if the program is cancelled. In the case of a cancellation, you will be notified by SRAI from srameetings@srainternational.org.

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Contributors

  • Debra Parrish, Partner, Parrish Law Offices, LLC

    Ms. Parrish is an attorney who works with academic medical centers, research institutions and companies, particularly those in the life sciences area in the United States. Her areas of legal concentration are science law (including research misconduct, regulations, compliance and investigations), health care law, and intellectual property. Ms. Parrish previously worked at the Office of Research Integrity as an attorney and now counsels journals, institutions and scientists on matters of research integrity. She is a frequent speaker and author on research integrity issues and has worked on some of the most high profile and complex cases over the past 25 years. In March 2016 she served as an invited panel member on research integrity issues at the National Academy of Sciences. She received her law degree and bachelor of science in biomedical engineering from Duke University and is a member of the patent bar.

May 16, 2024
Thu 2:00 PM EDT

Duration 1H 0M

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