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Event Description

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.

Don't wait to register for the When Does Validation Start?. You'll meet influential people and maximize your opportunities for success. Start now by accessing the information below.

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Event Details

Conference/Event Dates: 05/11/2016 - 05/11/2016
Classification: B2B
Primary Industry: Clinical Pharmacology
Other Industries: Clinical Pharmacology, Pharmaceutical, Professional Healthcare
Audience: Professionals involved in the development and manufacturing of FDA regulated drug products and devices from:

Pharmaceutical Companies
Biopharmaceutical Companies
Medical Device Companies

Booth Details

Booth Size Booth Cost   Available Amenities
No exhibiting.   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: n/a
Other Booth Sizes Available: n/a

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Mark Travers

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