This training course is designed to give pharmaceutical and biologic companies operating in the U.S. and EU an understanding of product safety and regulatory compliance. The course will include case studies of adverse events to illustrate the decision-making process and reasoning needed behind when and how to properly report incidents to regulatory authorities.
USFDA & EU Essentials of Drug Safety and Pharmacovigilance - India Seminar 2012 at Mumbai
5 - 7 March 2012, Mumbai, India
Introduction
Venue
TBD Hotel
TBD Hotel, Mumbai, India
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Organised by
GlobalCompliancePanel
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