Organizational Structure

Organizational Structure of CFDI for National Medical Product Administration (NMPA)

(I) Office

Take charge of administrative affairs and comprehensive coordination of CFDI. Formulate management system and development plan, and enforce them. Undertake meetings, official documents, seal, archive management, government affairs information, news & promotion, inspection and supervision, security and confidentiality, emergency management, letter handling, visit reception, and logistics support. Organize drafting of comprehensive documents. Organize and carry out foreign cooperation, academic exchanges and technical consulting services. Undertake other assignments designated by CFDI.

(II) Information Management Division

Take charge of construction and management of information system, database and website. Organize and carry out classified protection of information security. Undertake daily management of the quality management system of CFDI. Undertake other assignments designated by CFDI.

(III) Inspection Division I

Organize formulation and revision of the rules and technical documents on the relevant inspection of drug non-clinical research. Organize and conduct pre-approval inspection, for-cause inspection of drug R&D and drug registration related to pharmacological and toxicological researches, clinical pharmacology and human bioequivalence trials. Organize and conduct certification inspection of Good Laboratory Practice. Organize and conduct inspection of generic drug quality and efficacy consistency clinical trials. Undertake assessment, employment and other management work of relevant inspectors. Conduct overseas inspection, international (regional) exchange and cooperation, and relevant technical researches in related fields. Undertake other assignments designated by CFDI.

(IV) Inspection Division II

Organize formulation and revision of the rules and technical documents on the relevant inspection of drug non-clinical research. Organize and conduct pre-approval inspection, for-cause inspection of drug R&D and drug registration related to pharmacological and toxicological researches, clinical pharmacology and human bioequivalence trials. Organize and conduct certification inspection of Good Laboratory Practice. Organize and conduct inspection of generic drug quality and efficacy consistency clinical trials. Undertake assessment, employment and other management work of relevant inspectors. Conduct overseas inspection, international (regional) exchange and cooperation, and relevant technical researches in related fields. Undertake other assignments designated by CFDI.

(V) Inspection Division III

Organize formulation and revision of the rules and technical documents on the inspection of traditional Chinese medicines and biological products. Organize and conduct pre-approval inspection of drug of traditional Chinese medicines and biological products and for-cause inspection of production process. Undertake assessment, employment and other management work of relevant inspectors. Conduct overseas inspection, international (regional) exchange and cooperation, and relevant technical researches in related fields. Undertake other assignments designated by CFDI.

(VI) Inspection Division IV

Organize formulation and revision of the rules and technical documents on the inspection of chemical drugs. Organize and conduct approval inspection and production process for-cause inspection of chemical drugs. Undertake assessment, employment and other management work of relevant inspectors. Conduct overseas inspection, international (regional) exchange and cooperation, and relevant technical researches in related fields. Undertake other assignments designated by CFDI.

(VII) Inspection Division V

Organize formulation and revision of the rules and technical documents on the inspection of medical devices. Organize and conduct for-cause inspection of production process of medical devices. Undertake assessment, employment and other management work of relevant inspectors. Conduct overseas inspection, international (regional) exchange and cooperation, and relevant technical researches in related fields. Undertake other assignments designated by CFDI.

(VIII) Inspection Division VI

Organize formulation and revision of the rules and technical documents on the inspection of cosmetics. Organize and conduct for-cause inspection of R&D and production process of cosmetics. Undertake assessment, employment and other management work of relevant inspectors. Undertake relevant food inspections entrusted by the State Administration for Market Regulation. Conduct overseas inspection, international (regional) exchange and cooperation, and relevant technical researches in related fields. Undertake other assignments designated by CFDI.

(IX) Human Resources Division (Party Committee Office)

Take charge of construction of Party organization and personnel management of CFDI. Undertake cadre personnel, organization establishment, salaries and insurance, education and training and cadre supervision of CFDI. Undertake daily work of the Party Committee and the Commission for Discipline Inspection of CFDI. Formulate and organize implementation of work plans and systems of party construction and discipline inspection. Undertake Party organization construction, construction of the Party conduct and of an honest and clean government, discipline inspection and daily education management of party members, and supervision and enforcement of discipline of CFDI. Undertake management and consolidation of labor unions, the Communist Youth League, women's committees and other alliances. Undertake management and service of retirees. Undertake other assignments designated by CFDI.

(X) Finance Division

Take charge of financial management of CFDI. Take charge of budgeting, final accounting and budget execution monitoring. Take charge of funds management, daily financial management, and accounting and supervision of state-owned assets of CFDI. Undertake works related with housing reform. Undertake other assignments designated by CFDI.