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Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials

28 February 2012, Palo Alto, United States


Introduction
This 90-minute webinar will provide an overview of regulatory management for clinical trials. It will discuss key regulatory aspects of a clinical project such as clinical protocol management, IRB management, safety reporting, rules for recruitment programs, seeking advice from FDA, trial master files, and training requirements.

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Venue
Online Event

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

Useful links

Organised by
ComplianceOnline
Contact information
ComplianceOnline
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
+1-650-620-3915
Contact us by email

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