In this Clinical compliance training learn how to assess record and manage the adverse events occurring during conduct of clinical research utilizing human subjects and how to avoid the common mistakes.
How Accurate Adverse Event Reporting is the Key to Subject Safety of approved drugs
4 August 2010, Palo Alto, United States
Introduction
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Online Event
Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States
Organised by
ComplianceOnline
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