Graduate Certificate in Medical Devices Regulatory Affairs
GCMDRA is aimed at building a pipeline of executives, managers and directors to meet the immediate and long-term requirements of the Medical Technology Manufacturing industry. 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 those with portfolio in MD regulation and strategy development, and will further equip participants 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.