Graduate Certificate in Medical Devices Regulatory Affairs
This part-time and year-long programme is tailored for busy working professionals who wish to equip themselves with knowledge and experience in the global regulatory framework of the medical device (MD) industry. It is well suited for experienced executives, managers and directors with portfolio in MD regulation and strategy development.
GCMDRA is also relevant for current MDRA professionals who wish to enrich themselves with a global outlook where the role of a MD regulatory professional is examined systematically from the context of different regions. GCMDRA is organized by NUS Department of Biomedical Engineering.