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The DHF, DMR, DHR, and the Technical File / Design Dossier - Regulatory Requirements - Webinar By GlobalCompliancePanel

2 November 2011, Wilmington, United States


Introduction
The U.S. FDA's DHF
The EU's MDD and the Technical File / Design Dossier
Design Control vs. a Product 'Snapshot in Time'
DHF "Typical" Contents
TF / DD Expected Contents
Parallel Approaches to Documentation -- Teams
Future Directions
FDA and NB Audit Focus

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Venue
online training webinar

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

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Organised by
global compliance panel
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