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.
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
14 September 2011, Palo Alto, United States
Introduction
Venue
Online Event
Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States
Organised by
ComplianceOnline
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