To undertake drug quality supervision and inspection in Chengdu 19 districts (cities), counties and high-tech zones; To undertake the customs clearance inspection of drugs imported and exported by Chengdu Customs; To undertake the registration inspection of pharmaceutical research institutions and production enterprises applying for drug registration and medical institutions applying for preparation registration in Chengdu; As one of the 17 domestic drug inspection institutes recommended by the State Administration of Pharmaceutical Products to the Hong Kong government, it undertakes the registration and inspection of Chinese patent medicines in Hong Kong; To undertake entrusted inspection and technical consulting services for drugs and food; To undertake the research work on drug standards and new technologies for drug testing issued by the State Pharmacopoeia Committee; To undertake the training and technical guidance of technical personnel for drug and food quality control within its jurisdiction; Accept the judicial entrustment inspection within its jurisdiction; To undertake the inspection and testing of food, health care products and cosmetics within their respective administrative areas; Responsible for the collection, verification, statistics, feedback, analysis, reporting and other related technical work of adverse drug reaction reports within the city; Participate in the organization and coordination of adverse drug reactions, medical device adverse events and drug abuse in the gold market; Participate in the publicity, education and training of adverse drug reactions in the city; Participate in internal and external exchanges and cooperation in technical monitoring of drugs and medical devices; To undertake the inspection of agricultural inputs, agricultural production environment and quality and safety of agricultural products, including supervision, evaluation and sampling entrusted by quality and safety supervision departments of agricultural products at all levels. Undertake entrusted inspection, supervision inspection and arbitration inspection of pollution-free vegetables and seeds in Chengdu; Provide technical guidance to the district (city) and county seed quality inspection institutions.
Chengdu Food and Drug Information Center
Under the leadership of the US Food and Drug Administration in Chengdu, standardize and implement the informationization of food and drug supervision and management in Chengdu, and promote the development and application of e-government; Real-time monitoring of food and drug enterprises; Establish a special network for food and drug supervision and management and an information consulting service network to provide a safe e-government and e-commerce application environment for all food and drug-related administrative departments, enterprises and other relevant organizations and institutions; To formulate information planning, network and computer management rules and regulations for food and drug supervision and management, and undertake the design, development and construction of information applications and the design, development and maintenance of the portal website of the Food and Drug Administration; Responsible for the management, operation and maintenance of the central computer room, undertake global network security, computer technology maintenance and personnel training, collect and sort out e-commerce information, and assist the Food and Drug Administration in publishing external information online and making government affairs public; To undertake other tasks assigned by the US Food and Drug Administration.
Chengdu adverse drug reaction monitoring center
1, publicize and implement the Measures for the Administration of Adverse Drug Reaction Monitoring and related laws and regulations promulgated by the state;
2. To undertake technical work related to ADR monitoring such as the collection, verification, feedback, statistics and reporting of ADR reports in this Municipality, and report to Sichuan ADR Monitoring Center, Municipal Drug Administration and Municipal Health Bureau as required;
3. Organize and coordinate the monitoring of adverse drug reactions and medical device adverse events in Chengdu according to the overall deployment of the provincial adverse drug reaction monitoring center and the work plan of Chengdu US Food and Drug Administration;
4, establish and improve the area of adverse drug reaction monitoring network;
5. Organize publicity, education and training on adverse drug reactions in this Municipality, and edit and publish information bulletin and publications on adverse drug reactions in this Municipality;
6. Cooperate with the US Food and Drug Administration to inspect drug production and trading enterprises and medical and health institutions to carry out adverse drug reaction reporting and monitoring;
7. Assist superior departments to implement emergency measures to control adverse drug reactions, and investigate, confirm and handle cases of adverse drug reactions that need to be tracked;
8. Accept the business guidance of Sichuan Adverse Drug Reaction Monitoring Center and the specific management guidance of Chengdu US Food and Drug Administration.