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Maintaining Compliance of Clinical Sites with Regards to the FDA Draft Guidance on (Risk-Based Approach to Monitoring)

18 July 2012, Wilmington, United States


Introduction
Overview: Monitoring of clinical sites is a critical part of the Good Clinical Practices. With the advent of electronic data capture (EDC processes and more recently the FDA guidance, Oversight of Clinical Investigations-a Risk-based Approach to Monitoring some changes in the way we monitor sites and the data collection are taking place.
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Online Training

Online Training, 1000 N West Street, Suite 1200, DE | USA | 19801, Wilmington, 19801, United States

Organised by
GlobalCompliancePanel
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