Office
Responsibilities: comprehensive coordination and supervision of the administrative affairs of the Bureau; undertake secretarial, information, official, confidentiality, security, archives, letters and visits, foreign reception and other day-to-day government work; undertake the construction of information technology and statistics management; responsible for the Bureau's logistical support, asset management, financial management, internal audit, etc.; supervise and guide the direct units State-owned assets and financial management; organization and formulation of the system's capital construction and equipment and facilities planning.
Organization and Personnel Office
Responsibilities: assist the party committee responsible for the city's food and drug supervision and management system cadre management and leadership team building; responsible for personnel, staffing, and labor and wages, education and training; undertake the approval of visits and the introduction of foreign intelligence; responsible for the registration of licensed pharmacists, management, and the organization of the implementation of the evaluation of professional and technical positions in the pharmaceutical industry and practitioners of vocational qualifications access system; responsible for the Bureau and the agencies sent to the work of the Bureau of the state-owned assets and equipment planning. system; responsible for the Bureau and the dispatch of the agency retirees management and service work; organization, coordination and guidance of the system of grass-roots construction related work.
Policies and Regulations
Responsibilities: commissioned to draft local laws and regulations on drug supervision and management; commissioned in conjunction with the relevant departments to formulate local laws and regulations on the safety management of food, health care products, cosmetics; the development of a comprehensive supervision policy; organizations to carry out publicity and education of food and drug supervision and management of laws and regulations and supervise the implementation of the contractors to undertake the review of normative documents, administrative penalty cases, administrative penalty review, and supervision and management of the work of grassroots construction of the system. Administrative penalty case review, administrative reconsideration, administrative litigation, preside over the administrative penalty administrative licensing hearings, accepting complaints against the relative; responsible for the supervision of administrative law enforcement; responsible for the system of food and drug administration and law enforcement documents for processing; undertake the county (city), district food and drug supervision and management agencies normative documents and major administrative penalty case review for the record; organization of investigation and research, standardize administrative licensing and Open government work.
Food Safety Coordination and Supervision Department
Responsibilities: organization of the relevant departments to develop food safety management work planning and supervision of implementation; according to law, the exercise of comprehensive supervision of food safety management, organization and coordination of food safety management work undertaken by the relevant departments; the comprehensive coordination of food safety testing and evaluation; in conjunction with the relevant departments to develop the analysis of food safety information, forecasting and publishing methods; undertake research and coordination of food safety management work. Measures; undertake research and coordination of food safety unified standards; coordinate with relevant departments to establish and improve the food safety accident reporting system, organize and carry out the investigation and handling of major accidents; coordinate the implementation of food safety special law enforcement supervision and inspection activities, with the relevant departments to carry out emergency rescue work; organize the development of food safety and major technical supervision methodology, means of scientific research and planning and supervision of the implementation. Undertake the daily work of the Ningbo Food Safety Commission Office.
Health Food and Cosmetics Supervision
Responsibilities: implementation of national, provincial and municipal laws, rules and regulations relating to health care products, cosmetics supervision; the development of health care products, cosmetics, comprehensive supervision policy, work planning; according to law, exercise of health care products, cosmetic safety management and comprehensive supervision responsibilities, organization and coordination of health care products, cosmetics safety management work undertaken by the relevant departments; Coordination of health care products, cosmetics safety special law enforcement and supervision activities; implementation of national health care market access standards; supervision and implementation of health care production quality management standards; review of health food advertisements; health care licensing in accordance with the relevant work.
Drug Safety Supervision and Registration Division
Responsibilities: supervise the implementation of statutory standards for drugs; organize and implement the drug classification and management system; supervise the implementation of the quality of non-clinical research, clinical trial quality, quality of drug production, the quality of traditional Chinese medicine, the quality of preparations for medical units of the management norms; responsible for drug non-clinical research institutions and drug clinical trial base qualification certification applications for the first instance; Responsible for accepting the declaration and transfer of new drugs, generic drugs and protected varieties of traditional Chinese medicine; supervising new drug research institutes; supervising narcotic drugs, psychotropic drugs, toxic drugs for medical use, detoxification drugs, radiopharmaceuticals, preparations for medical units, diagnostic reagents, and materials and containers used for pharmaceutical packaging; commissioned to undertake the on-site review of the conditions for the opening of drug manufacturing enterprises and preparatory laboratories for medical units; supervising the implementation of the adverse drug reaction Monitoring system; guide the business of drug testing organizations; fulfill the "Drug Import Management Measures," the responsibilities of the Ningbo port drug import filing.
Drug Circulation Supervision Department
Responsibilities: implement the national drug circulation laws, rules and regulations and local drug circulation supervision and management laws and regulations; supervise the implementation of prescription drugs, non-prescription drugs and Chinese herbal medicines, Chinese medicinal herbs, Chinese herbal medicinal tablets, purchase and sale of regulations and quality management standards for drug business; in accordance with the law to issue drug retail chain enterprises, drug retail enterprises (drug retail chain enterprises stores) of the Business License"; commissioned to undertake on-site acceptance of drug wholesalers, inspection of drug advertisements; supervision of urban and rural markets Chinese herbal medicines trading and drug production and management enterprises set up offices within the jurisdiction.
Medical Devices Division
Responsibilities: supervise the implementation of medical devices, in vitro diagnostic reagents, medical biomaterials, sanitary materials, product standards and product classification and management directory; issuance of the first class of medical device product registration certificate; supervise the implementation of the registered product standards; responsible for the production of first-class medical devices, business enterprise registration, commissioned to undertake the second, the third class of medical devices production and management enterprise license review and approval. The company is responsible for the registration of the first class medical device production and management enterprises; entrusted to undertake the second and third class medical device production and management enterprise license review and approval and start-up conditions of the on-site audit; supervise the implementation of quality management standard for the production of medical devices, commissioned by the implementation of the quality system assessment of medical devices and product safety certification; supervise and inspect the medical device advertisements; responsible for the monitoring of adverse events of medical devices; supervise the production of medical devices, the operation of medical devices in the region set up by the office; guidance for the detection of medical devices The medical device manufacturers and operators of medical devices to set up offices in the area under their jurisdiction; guide the medical device testing organizations.