Internal organs of Shijiazhuang Food and Drug Administration

According to the above responsibilities, Shijiazhuang Food and Drug Administration has 11 internal organs:

(1) The office

is responsible for the overall coordination of the daily affairs of the organs, and is responsible for secretarial work, filing, duty, letters and visits, confidentiality, government information management, organization of important meetings, etc. To undertake the administrative and logistical work of the organs; Responsible for the organization and coordination of emergency management; To formulate departmental development plans and organize their implementation; To be responsible for the work of retired cadres in organs and guide the work of retired cadres in directly affiliated units.

(II) Personnel and Education Department

is responsible for the organization, staffing, personnel management, salary and training of organs, agencies and directly affiliated units; According to the provisions of the organization and implementation of licensed pharmacist qualification system, food and drug related professional and technical post evaluation and practitioners' professional qualification access system; Responsible for the training of relevant personnel of food and drug supervision and management in the city.

(3) Financial Equipment Department

is responsible for drafting the management system of finance, accounting, equipment, fixed assets and capital construction in the bureau and organizing its implementation; Responsible for financial management and accounting affairs such as budget and final accounts, financial revenue and expenditure of organs and directly affiliated units; Carry out internal audit and supervision and management of branches.

(4) Policy and Regulation Department

organizes policy research on food and drug supervision and management; Participate in the drafting of local laws and regulations; Responsible for administrative law enforcement supervision; Undertake administrative reconsideration, administrative litigation and hearing; Responsible for the examination of administrative punishment cases and the filing of major administrative punishment cases; Responsible for improving the statutory health examination system for employees in catering and pharmaceuticals in the city and supervising the implementation; Responsible for news propaganda; To guide the legal system construction and legal publicity and education.

(5) The Food Supervision Department

is responsible for the licensing, supervision and management of catering services; Supervise the implementation of food safety management standards for catering services, and investigate and deal with food safety accidents in catering services according to law; Assist relevant departments to collect food safety risk assessment information and materials for catering services.

(6) Cosmetic Health Food Supervision Department

Responsible for the administrative licensing of health food and cosmetics according to regulations; Responsible for the supervision and management of health food and cosmetics; Supervise the implementation of the relevant standards for the safety management of health food and cosmetics; Responsible for the registration of health food and cosmetics and related matters according to regulations; Organize to investigate and deal with cosmetic health food safety accidents according to law.

(7) The Drug Registration Office

is responsible for the acceptance and reporting of medical institutions' applications for preparation; To be responsible for reviewing and reporting the forms of re-registration data of pharmaceutical preparations in medical institutions; Responsible for completing the on-site verification of the application for registration of designated drugs, preparations from medical institutions, packaging materials for direct contact with drugs and containers; Responsible for the daily supervision, management and supervision of sampling work of enterprises that are in direct contact with pharmaceutical packaging materials and containers.

(8) The Medical Device Supervision Office

issues the first-class product registration certificate of medical devices according to law; To organize the implementation of national laws, regulations and rules on medical devices; Investigate and deal with illegal acts according to law; Implementing the classified management of medical device products and the quality management norms of production and operation; Responsible for the monitoring and re-evaluation of adverse medical device reactions; According to the law, supervise and supervise the research, production, management and use of medical devices within the jurisdiction.

(9) The Drug Safety Supervision Department

is responsible for organizing and implementing the classified management of prescription drugs and over-the-counter drugs; Organize the monitoring of adverse drug reactions and drug abuse; Supervise the implementation of quality management standards for drug production, preparation quality of medical institutions and production quality of Chinese herbal pieces; Responsible for the supervision and management of pharmaceutical production enterprises and pharmaceutical preparation rooms of medical institutions; To be responsible for the preliminary examination, supervision and management of entrusted drug production; Supervise the production and use of radioactive drugs, narcotic drugs, toxic drugs for medical use, psychotropic drugs, pharmaceutical precursor chemicals and drug rehabilitation drugs in pharmaceutical production enterprises according to law; Responsible for supervising the implementation of national drug standards, preparation standards of medical institutions and processing specifications of Chinese herbal pieces; To guide the business work of drug inspection institutions within their respective jurisdictions.

(1) The Drug Market Supervision Department

issues licenses for drug retail enterprises (including chain enterprises) according to law, and examines and approves drug retail chain enterprises to engage in the second-class psychotropic drug business; Responsible for organizing the implementation of the quality management standards for pharmaceutical retail enterprises; Supervise the operation of narcotic drugs, toxic drugs for medical use, psychotropic drugs, drug rehabilitation drugs and pharmaceutical precursor chemicals according to law; Responsible for the supervision and management of pharmaceutical trading enterprises; Responsible for the classified management of prescription drugs and over-the-counter drugs in the field of drug circulation; Supervise the professional market of Chinese herbal medicines and engage in Internet drug information service units according to law; Investigate and deal with illegal drug business according to law; Responsible for the monitoring, inspection, transfer and summary of illegal drug advertisements.

(11) The Drug Inspection Office

implements the supervision, management and inspection system for drugs and medical devices, and investigates and deals with illegal acts of drugs and medical devices according to law; Organize the implementation of the city's drug quality sampling; Responsible for the supervision and management of drug users; Participate in the special law enforcement supervision and inspection activities of drug safety in the city; To guide and supervise the drug inspection, law enforcement and emergency disposal of county (city) and district food and drug supervision and management institutions; Organize and implement the destruction of counterfeit and inferior drugs, handle product recalls of cases and investigate and deal with cases; Accepting complaints and reports on drugs and medical devices, and inspecting violations of laws and regulations according to law.

the party Committee of the organ

is responsible for the party-mass work of the organ and its directly affiliated units.

the discipline inspection (supervision) room

is responsible for the discipline inspection (supervision) work of organs and directly affiliated units.