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Session Chair(s)
Jonathan Seltzer, MD, MA, MBA, FACC
Chief Scientific Officer
WCG, United States
Learning Objective : Describe the rationale for convening an endpoint adjudication committee (EAC); Recognize the principal regulatory and practical considerations underlying a well-run EAC from CRO, sponsor, and agency perspectives; Identify and discuss how to apply at least three EAC best practices into clinical development.
Speaker(s)
Panelist
Douglas Burgener
Biofourmis, United States
Sr. Marketing Director
Panelist
Debra Montgomery, MSN, RN
Duke Clinical Research Institute, United States
eCRF Librarian, CDS III
Panelist
Nicole Pushlar
Boehringer Ingelheim Pharmaceuticals, Inc., United States
Clinical Scientist, Clinical Trial Management
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