This combined Quality Agreement and DMF (Drug Master Files) training will discuss the advantages for suppliers and drug product manufacturers developing these arrangements together.
Quality Agreements with Pharmaceutical - Biologic Manufacturers and the Use of Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities - Webinar By GlobalCompliancePanel
8 December 2011, Wilmington, United States
Introduction
Venue
online training
online training, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States
Useful links
Organised by
global compliance panel
Contact information
Mr webinars
online training, 1000 N West Street,Suite 1200, DE, Wilmington, 19801, United States of America
8004479407
Contact us by email
online training, 1000 N West Street,Suite 1200, DE, Wilmington, 19801, United States of America
8004479407
Contact us by email
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