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Regulatory Affairs Part II: The NDA Phase

8 - 10 March 2010, Horsham, United States


Introduction
Gain insight into the regulatory background of the NDA, preparing an NDA, and postapproval activities. The course focuses on drug and well characterized biological products and not the regulatory process for devices, generic products, or traditional biologics.
Venue
Drug Information Association, Inc.

Drug Information Association, Inc., Horsham, 19044, United States

Organised by
Drug Information Association
Contact information
Susan Mazak
+1 215-442-6183
Contact us by email

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