Regulatory bodies are demanding more strict regulations for the biopharmaceutical industries due to the potential adverse effects of biopharmaceutical products. This webinar will discuss about the biopharma industry best practices to comply with the regulations. It will also cover the recent regulatory updates and practical GMP tips on how pharmaceutical and biopharmaceutical companies can ensure.
Pharma and Biopharma Quality System Requirements Training
11 January 2013, Palo Alto, United States
Introduction
Venue
OnlineEvent
OnlineEvent, Palo Alto, 94303, United States
Useful links
Organised by
Tanvir Mahmud
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