This adverse event reporting Webinar/training will discuss the clinical trial regulations requirements with respect to adverse event and explain how to assess and report AEs and SAEs.
Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs
19 October 2010, Palo Alto, United States
Introduction
Venue
Online Event
2600 E. Bayshore Road, Online Event, Palo Alto, 94303, United States
Organised by
ComplianceOnline
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