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China NMPA Medical Device Regulartory Process Overview

07/08/2020 10:00am - 1:00pm

Planning to sell your medical device (including in vitro diagnostic (IVD) device) in Mainland China?

If so, you will need to register and file them with the relevant regulatory authority, the National Medical Products Administration (NMPA) (formerly the China Food and Drug Administration (CFDA)).

What should R&D companies in Hong Kong do before beginning the registration process?

Find out more HERE.


  • Start Date: 07/08/2020 10:00am

  • End Date: 07/08/2020 1:00pm