(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 people's government at the same level, organize and coordinate the special law enforcement and supervision activities of food, health care products and cosmetics safety; Organize, coordinate and cooperate with relevant departments to carry out emergency rescue 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.
(five) to supervise the implementation of the laws, regulations and rules of the state and local regulations and rules on drug supervision and management; Formulate normative documents related to drug supervision and management and supervise their implementation.
(six) to supervise the implementation of the legal standards for drugs, medical devices and packaging materials; Supervise the implementation of the classified management system for prescription drugs, over-the-counter drugs and medical devices; Supervise the implementation of adverse drug reaction monitoring system and cooperate with the implementation of adverse drug reaction monitoring of medical devices; Supervise the implementation of quality management standards for drug production, drug management, production of Chinese herbal pieces, preparations of medical institutions, non-clinical research of drugs and clinical trials of drugs.
(seven) responsible for the issuance and management of drug retail and chain enterprise licenses; Handle the registration of Class I medical device manufacturers and issue Class I medical device product registration certificates; According to the authorization, go through the formalities of drug production, preparation license of medical institutions and purchase and use of special drugs; Authorized by the Provincial Bureau, responsible for the issuance and management of medical device business licenses.
(eight) according to the daily supervision of drugs, medical devices, packaging materials production, management and use of units, according to the provisions of supervision and spot checks on the quality of drugs, medical devices and packaging materials, investigate and deal with violations of drug supervision and management laws, regulations and rules.
(nine) according to the supervision of toxic drugs, narcotic drugs, psychotropic drugs, radioactive drugs, drug rehabilitation and special medical devices; Responsible for the inspection and investigation of drugs and health food advertisements in this area.
(ten) responsible for food, health care products, cosmetics safety comprehensive supervision related laws and regulations training and drug supervision and management related laws and regulations training; Organize and implement the qualification system for licensed pharmacists.
(eleven) the management of drug inspection and testing institutions and the following food and drug supervision and management institutions.
(twelve) to undertake other related matters assigned by the US Food and Drug Administration and the people's government at the same level.