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Investigator responsibilities and Legal commitments in Drug and Device Clinical Research

14 September 2011, Palo Alto, United States


Introduction
This webinar will focus on the principal investigator's role and responsibilities, the legal language of FDA form 1572 or Device equivalent and how you can ensure a celan audit by following GCP.
Venue
Online Event

Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States

Organised by
ComplianceOnline
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