Pharmaceutical Quality and Regulatory Affairs

Description

manufacture, regulations and quality standards for the pharmaceutical and ATMP, GMP guidelines, Market access

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This five-day course provides an overview of manufacture, regulations and quality standards for the pharmaceutical and advanced therapy medical products (ATMP) industry. You’ll learn about current best good manufacturing practice (GMP) in the UK/Europe and the rest of the world, dossier submission and assessment and revisions to (GMP) guidelines. It will help you facilitate swift and safe access to markets, through successful submissions and examination processes.

Pharmaceutical Quality and Regulatory Affairs