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.