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

欧美AV

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Regulatory Affairs Part II: The NDA Phase

8 - 10 March 2010, Horsham, United States

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