Regulatory Framework on Medical Device Development and Clinical Trials

Published on : 18-Apr-2013
17-May-2013 - 17-May-2013 0900hrs - 1700hrs

VENUE : Biopolis, Breakthrough & Discovery Theatrette, Level 4 , Matrix Building 30 Biopolis Street, Singapore 138671

Contact Information :

Dr. Michelle Ngiam




Compliance to regulatory guidelines is paramount to the success of the development of a medical device, which would lead to its commercialization and clinical adoption. This jointly-organised seminar by A*STAR and HSA aims to address the concerns and questions from the scientific and clinical community regarding the Singapore’s regulatory framework and standards for medical devices from pre-clinical to clinical trials and development & manufacturing.  Through this, the researchers, academics and clinicians would be able to gain a better understanding of the current regulatory guidelines when developing innovative solutions for today’s healthcare needs.

This seminar bring together an exciting list of speakers from both the public and private sectors, including expertise and regulatory professionals from HSA, TUV SUD, Innoheart, WEB Biotechnology, DH Reg Sys etc.

Click here to register!

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