(1) Organizing relevant departments to draft laws and administrative regulations on the safety management of food, health products and cosmetics; Organize relevant departments to formulate comprehensive supervision policies and work plans for food, health care products and cosmetics safety management and supervise their implementation.
(two) to exercise the comprehensive supervision duties of food, health care products and cosmetics safety management according to law, and organize and coordinate the safety supervision of food, health care products and cosmetics undertaken by relevant departments.
(three) to organize the investigation and handling of major safety accidents of food, health care products and cosmetics according to law; According to the authorization of the State Council, organize and coordinate the national food, health care products, cosmetics safety special law enforcement supervision activities; Organize, coordinate and cooperate with relevant departments to carry out emergency rescue work for major accidents of food, health care products and cosmetics.
(four) comprehensive coordination of food, health care products and cosmetics safety testing and evaluation; In conjunction with the relevant departments, formulate measures for the release of food, health care products and cosmetics safety supervision information and supervise the implementation, and regularly and comprehensively release the food, health care products and cosmetics safety information of relevant departments to the society.
(5) Drafting laws and administrative regulations on drug administration and supervising their implementation; Implement the protection system of traditional Chinese medicine varieties and the administrative protection system of drugs according to law.
(6) Drafting laws and administrative regulations on the management of medical devices and supervising their implementation; Responsible for the registration, supervision and management of medical device products; Draft relevant national standards, formulate and revise industry standards and production quality management norms for medical device products, and supervise their implementation.
(7) Drug registration, drafting, revising and promulgating national drug standards; Formulate market access standards for health care products and be responsible for the examination and approval of health care products; Formulate a classified management system for prescription drugs and over-the-counter drugs, establish and improve a monitoring system for adverse drug reactions, and be responsible for drug re-evaluation, evaluation of eliminated drugs, and formulation of a national list of essential drugs.
(eight) to formulate and revise the quality management standards for drug research, production, circulation and use, and supervise the implementation.
(nine) to supervise the quality of drugs and medical devices in production and operation enterprises and medical institutions, and regularly publish national quality bulletins on drugs and medical devices; Investigate and deal with illegal activities such as manufacturing and selling counterfeit and inferior drugs and medical devices according to law.
(ten) according to the supervision of radioactive drugs, narcotic drugs, toxic drugs, psychotropic drugs and special medical devices.
(eleven) to formulate and improve the qualification access system for licensed pharmacists, and supervise and guide the registration of licensed pharmacists.
(twelve) to guide the national drug supervision and management and the comprehensive supervision of food, health care products and cosmetics safety management.
(thirteen) to carry out exchanges and cooperation between governments and international organizations related to drug supervision and management and food, health care products and cosmetics safety management.
(fourteen) to undertake other tasks assigned by the State Council.