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Discussion with Former Center for Devices and Radiological Health (CDRH) Management
Program Code:
164
Date:
Monday, June 25, 2012
Time:
3:30 PM to 5:00 PM
EST
CHAIR
:
Daniel Schultz, Greenleaf Health, LLC, United States
PRESENTER
(S):
David Feigal, NDA Partners, LLC, United States
Timothy Ulatowski, Becker & Associates Consulting, Inc., United States
Dr. Donna-Bea Tillman is a senior consultant at Biologics Consulting Group with 17 years of medical device regulatory experience at the US Food and Drug Administration, Center for Device and Radiological Health.
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Description
Join this moderated panel discussion with former CDRH Directors and Management. The session will focus on the evolving face of medical devices, the interface between drugs and devices, new challenges and opportunities, and the changing regulatory landscape.
Learning Objectives:
Identify the new challenges and evolving face of medical devices
Explain the interface between drugs and devices
Describe the changing regulatory landscape.