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EVENT DATE
May 2016
MoTuWeThFrSaSu
      1
2345678
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3031     

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Overview

In the process of drug development, when should you start Good Manufacturing Practices (GMP) Validation activities? What level of these activities are recommended or required at the different stages of drug development? These stages include; development, clinical phases, and commercialization. The information in this presentation provides assistance with the development of a Validation Program and Validation Master Plan.

This presentation will discuss what level of Validation is required at the different stages of the pharmaceutical product development lifecycle.

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