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.
Maintaining Compliance of Clinical Sites with Regards to the FDA Draft Guidance on (Risk-Based Approach to Monitoring) - Webinar By GlobalCompliancePanel
18 July 2012, Wilmington, United States
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Online Training, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States
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