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Session Chair(s)
Peter Richard Arlett, MD, FFPM, FRCP
Head Data Analytics and Methods Task Force
European Medicines Agency, Netherlands
Learning Objective : Distinguish the different approaches taken by EMA and FDA to address common challenges; Identify the complementary approaches to using common tools including the Periodic Benefit Risk Evaluation Reports (PBRER) and the planning of data collection; Recognize how EMA and FDA collaborate on the safety of specific drug reviews and on the development of procedures and guidance.
Speaker(s)
FDA Perspective
Gerald Dal Pan, MD, MHS
FDA, United States
Director, Office of Surveillance and Epidemiology, CDER
Industry Perspective
Valerie E. Simmons, MD, FFPM
Eli Lilly and Company Ltd, United Kingdom
Senior Medical Fellow, Global Patient Safety
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