Department of Medical Device Registration Administration

2019-05-27

Organizing the drafting and supervising the implementation of medical device standards, classification rules, naming rules and coding rules, and drawing up and implementing the administration system of medical device registration.
Department of Drug Supervision and Administration

2019-05-27

rganizing the drafting and supervising according to its functions the implementation of GMP for drugs, and organizing the drafting and guiding the implementation of operation and use quality management practices.
Department of Drug Registration Administration

2019-05-27

Organizing the drafting and supervising the implementation of Chinese Pharmacopoeia and other drug standards, and technical guidelines, and drawing up and implementing the drug registration administration system.
Policy and Regulation Department

2019-05-27

Researching major policies on the supervision and administration of drugs, medical devices, and cosmetics.
Department of General Affairs, Planning, and Finance

2019-05-27

Being responsible for the routine operation of the National Medical Products Administration (hereinafter referred to as the "NMPA"), and undertaking information, security, file, confidentiality, public complaints and proposals, government affairs openness, statistics, informatization, news and publicity, and other work.

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