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Ensure the Safety of Clinical Trials: The Roles of Data Safety Monitoring Boards (DSMB) and Institutional Review Boards (IRB) - Webinar By GlobalCompliancePanel

1 December 2011, Wilmington, United States


Introduction
This presentation will review the definition, purpose, composition, guiding documents, responsibilities of DSMB, its role in the Data and Safety Monitoring Plan, the role of IRBs and DSMBs in clinical studies, PI's responsibility of AE reporting, and finally discuss which studies would benefit from the DSMB's involvement.

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Venue
online training

online training, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States

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Organised by
Global compliance panel
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