Graduate Certificate in Medical Devices Regulatory Affairs
This 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. The role of a regulatory professional will be examined systematically from the context of different regions. The programme is best suited for experienced executives, managers and directors with portfolio in MD regulation and strategy development. It is also relevant for professionals who wish to expand on their MD regulatory knowledge with a global outlook. GCMDRA is organized by NUS Department of Biomedical Engineering.