According to the above responsibilities, the Municipal Food and Drug Administration has eight internal organs:

(1) Office.

comprehensively coordinate the daily work of the bureau; Take the lead in formulating various rules and regulations of the organs; Coordinate the implementation of the annual work target responsibility system; Organize and coordinate emergency response; To undertake the daily work such as messages, important meetings, government information, confidentiality, archives, letters and visits, proposals, publicity, security, administrative logistics, information construction, etc. To undertake the preparation and implementation of the budget of the bureau, as well as the purchase and management of fixed assets and technical equipment; To undertake the guidance, supervision and inspection of state-owned assets and finance of directly affiliated units.

(2) organize the personnel department.

To undertake the organization establishment, personnel organization and team building of the Bureau and its directly affiliated units; Guide the system to carry out professional training for cadres and professional knowledge training for administrative counterparts; Organize the implementation of the professional qualification system for licensed pharmacists (licensed pharmacists) and employees of pharmaceuticals, medical devices, health food, cosmetics and catering services, as well as the evaluation of related professional and technical positions.

(3) Policy and Regulation Department.

To draft local laws and regulations on food safety supervision and management of drugs, medical devices, health foods, cosmetics and catering services; Guide the promotion of administration according to law and publicity and education; To undertake the review of the administrative normative documents of this department; To undertake the supervision of administrative law enforcement, relevant administrative reconsideration, administrative litigation, administrative penalty hearing, etc.; Organize and coordinate the city-wide law enforcement inspection of food safety of drugs, medical devices, health foods, cosmetics and catering services and the supervision of major cases and trans-regional cases.

(4) administrative examination and approval department.

to undertake the administrative licensing work and non-administrative licensing examination and approval of drugs, medical devices, health food, cosmetics and catering services in this department according to the prescribed authority, undertake the relevant work of drug import filing at Hangzhou port, and undertake the relevant licensing work organized and implemented by the food and drug supervision and administration department at a higher level.

(5) Food and beverage service supervision department (hanging the brand of health food and cosmetics supervision department).

supervise the implementation of quality management standards for the production and operation of health food and cosmetics and food safety management standards for catering services, organize the implementation of quantitative classification management system for food safety for catering services, supervise the implementation of food safety standards for catering services, organize the implementation of food safety guarantee for major events, and participate in the investigation and handling of major food safety accidents for catering services; To undertake the safety inspection and evaluation, risk assessment and emergency disposal of health food, cosmetics and catering service food; Supervise the implementation of the monitoring system for cosmetic adverse reactions; To guide the food safety of catering services, the daily supervision of health food and the hygiene supervision of cosmetics; Guide the business work of the city's health food, cosmetics, catering service food safety inspection and testing institutions.

(6) Drug Safety Supervision Department.

supervise the implementation of legal standards for drugs, preparations of medical institutions, packaging materials and containers that directly contact drugs; Supervise the implementation of quality management standards for drug non-clinical research, drug clinical trials, Chinese herbal medicine production, drug production and preparation of medical institutions; To supervise the production, operation and use of packaging materials and containers for narcotic drugs, psychotropic drugs, toxic drugs, radioactive drugs, preparations of medical institutions and drugs in direct contact; Supervise the production of drug-induced stimulants and pharmaceutical precursor chemicals; Cooperate with relevant departments to implement the national essential drug system and organize the implementation of the drug classification management system; To undertake drug production safety testing and evaluation, risk assessment and emergency response; Supervise the implementation of adverse drug reaction monitoring system; To guide the daily supervision of pharmaceutical production enterprises; To guide the business work of drug inspection and testing institutions in the city.

(7) drug circulation supervision department.

supervise the implementation of the quality management standards for pharmaceutical trading; Supervise the implementation of the classified management system for prescription drugs and over-the-counter drugs in the circulation field; Supervise the implementation of the rules for the purchase and sale of Chinese herbal medicines in urban and rural markets; Supervise and manage the operation and use of drug-induced stimulants and pharmaceutical precursor chemicals; Organize and implement the supervision of the quality of drugs used by medical institutions, and participate in the supervision and management of centralized drug procurement; Organizing and implementing the supervision of drug information services and transactions on the Internet; To undertake drug circulation safety testing and evaluation, risk assessment and emergency response; Guide the daily supervision of pharmaceutical trading enterprises.

(8) Medical Device Supervision Office.

supervise the implementation of legal standards for medical device products; Supervise the medical device production and management enterprises to organize production and management in accordance with the corresponding quality management norms or management requirements; Supervise medical institutions to abide by the management regulations in the procurement, storage and use of medical devices; Supervise the implementation of the medical device adverse event monitoring system; Entrusted with the implementation of medical device quality system assessment; To undertake the safety testing and evaluation, risk assessment and emergency disposal of medical devices; Guide the daily supervision of medical device production and operation enterprises; Guide the business work of medical device inspection and testing institutions in the city.

the party Committee of the organ. To be responsible for the work between the Party and the masses of the bureaus and directly affiliated units.