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.
Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials
28 February 2012, Palo Alto, United States
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Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States
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ComplianceOnline
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