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.
|Conference/Event Dates:||05/11/2016 - 05/11/2016|
|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:
Medical Device Companies
|Booth Size||Booth Cost||Available Amenities|
|Marketing Vehicles Allowed:||n/a|
|Other Booth Sizes Available: n/a|
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