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Medical Device Regulatory Updates For Major Markets & Clinical Trials For IVD

12/10/16 - 12/10/16

During the 12th of October 2016, the Pre-Event Medical Device Regulatory Updates For Major Markets & Clinical Trials For IVD  training course was held in conjunction with the Diagnostics Summit 2016.  The course provided us with a detailed overview of the regulatory requirements for all of the major global markets including Europe, the USA, China and SE Asia.

Our principal consultant, Ms. Tan Hwee Ee presented on Medical Device Regulatory Requirements For Europe/USA.

 



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