2024 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.

 

Poster

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

Programme

 To be advised

Fees

 

Click here to find out more about the Course Fees.

Continuing Education Credits

The Centre of Regulatory Excellence is an accredited provider for Continuing Professional Education (CPE) for Pharmacists and Continuing Medical Education (CME) for Doctors.

Continuing education credits are available for CoRE events through the Singapore Pharmacy Council and the Singapore Medical Council subject to their respective approvals.

Attendees who wish to avail of the credits are required to sign the relevant registration form along with their CPE/CME number on the day of the events.

Should the event be conducted online, please provide your CPE/CME number in the respective e-registration form.

The attendee’s registration details will be submitted after the event and credited upon receiving respective approvals.