
CFDA Medical Device Registration
Testing of Medical Device
Clinical Trial of Medical Device
Act as China Agency office
The State Food and Drug Administration (SFDA) of China requires that all medical device, companies with no location in the People's Republic of China appoint a registered Legal Agent (LA, in-country regulatory representative) and After Sales Service Agent(ASA). Appointed SFDA LA and ASA must be a legal entity and maintain a place of business in