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2025 GMS5004 Regulation of Pharmaceutical Manufacturing

Ensuring quality of healthcare products is one of the key pillars in regulatory responsibilities, for industry, manufacturers and regulators. The contribution of Chemistry, Manufacturing and Controls (CMC) to a successful control of quality in pharmaceutical products spans from product development and manufacture, process validation to post-market variation changes, as well as an optimal quality management system. 

This course provides the foundation in understanding the regulatory science behind the development, manufacturing and control of pharmaceuticals, including the global guidances that shapes the regulatory processes.  Besides promoting good submissions and evaluation practices, the course aims to enhance regulatory convergence and cooperation on CMC regulation.

Due to the limited availability of seats, early registration is strongly recommended.

Flyer_2025 GMS5004 Regulation of Pharmaceutical Manufacturing - with stamp

Click here for a step by step guide on how to register.
   


Date and Time


17 Nov 2025 @ 08:30 - 21 Nov 2025 @ 17:30

Speaker


 

Venue


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