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Graduate Certificate in Medical Devices Regulatory Affairs

Succeed in the Complex Global Regulatory Environment


    Demand for safe, effective and affordable healthcare products, advanced diagnostic tools and improved outcomes is increasing around the world. As such, skilled regulatory professionals are much sought after globally.

    Singapore has become an important hub for medical technology development. As such, it provides a good base for this unique program where regulatory professionals can deepen their technical knowledge and sharpen their application skills necessary to face an increasingly complex global regulatory framework.

    The Graduate Certificate in MDRA draws on the teaching and research excellence of NUS/BME faculty and combines the expertise of RAPS’ renowned regulatory leaders from around the world to provide you with the knowledge, skills and tools to succeed. The curriculum is based on the validated competencies of working regulatory professionals and is delivered through a combination of online training, interactive seminars, peer interaction and case study-based learning—all in a flexible format that fits your busy schedule.

    Click here to download a copy of the brochure.

    Click here to download a copy of the GCMDRA 2015/2016 Mini Brochure.


    Presented by:
    Department of Biomedical Engineering, Faculty of Engineering, National University of Singapore
    In partnership with the Regulatory Affairs Professionals Society

    Programme administrator :
    Office of Professional Engineering & Executive Education
    Faculty of Engineering, National University of Singapore
    3 Engineering Drive 2, Blk E1, #05-15, Singapore 117578