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.