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Key Aspects of the Trial Master File and How to Pass FDA Inspection - Webinar By GlobalCompliancePanel

3 November 2011, Wilmington, United States


Introduction
This presentation will help with preparing the site and the study team with how to successfully prepare for an audit, how to identify risk of noncompliance, what to do before, during and after an audit. All these are done with the primary goal in mind: getting no audit findings.

Useful links

Venue
online training webinars

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

Useful links

Organised by
Global compliance panel

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