Tianjin Food and Drug Administration set up 13 functional divisions (rooms):

(A) Office

Responsible for organizing and coordinating party affairs, government work, organization and coordination of the Bureau of organs and affiliated units of the comprehensive affairs. Responsible for the Bureau of medium- and long-term major comprehensive development planning, organization and preparation of annual work plan; organization of drafting leadership speeches, comprehensive reports and other important manuscripts. Responsible for the operation of party and government documents, verification and seal management; bear the bureau organs, archives management, party and government information management, open government information management, open government management. Responsible for the organization of major meetings, central group study, bureau meeting and director's office. Responsible for supervising and overseeing the work approved by the superior leaders. Responsible for the organization and coordination of the Bureau of emergency management and daily management (including the Bureau of duty management). Undertake the Bureau of news release, publicity and reporting, newspaper publishing and other work under the management. Organize the handling of people's letters and visits and the National People's Congress suggestions, CPPCC members proposals. Responsible for the bureau system information construction work, organization, guidance bureau information construction implementation and application management. Responsible for the Bureau liaison reception, foreign affairs administration and organization of external exchanges and cooperation and other institutional affairs work. Responsible for the bureau's meetings, statistics, confidentiality, security, comprehensive management, the Red Cross, the Association and other associations of the work of the centralized management. Responsible for guiding the business of the Bureau's information center. Undertake the work of the Bureau temporarily assigned.

(B) Policies and Regulations

Organize policy research on supervision and management of drugs, medical devices, health food, cosmetics and food service food safety. Propose legislative planning and program recommendations. Participate in the drafting of food and drug supervision and management of relevant local laws and regulations, draft regulations. Undertake the bureau normative documents legality audit, filing and organization of cleaning, assessment work. Undertake the review of major cases and organize the case review meeting of the Bureau. Undertake administrative law enforcement supervision. Undertake the organization of administrative reconsideration, administrative appeals and hearings. Guiding the construction of legal system of the system. Organize and carry out the publicity work of relevant laws and regulations. Organize the system of administrative approval system reform. Undertake the work of the Bureau temporarily assigned.

(C) Food Service Supervision

Implementation of national laws, regulations, rules and guidelines on food safety supervision and management of food service, supervision and management of the formulation of policies, normative documents, draft legislation and supervision and implementation. Undertake food service food safety supervision and management work, and organization, guidance and coordination of the sub-bureaus to do a good job in the area of food service food safety supervision and management work. Undertake investigation and monitoring of food service food safety conditions and release information related to food service food safety supervision. Supervise the implementation of food service food safety standards and management norms. Responsible for food service food safety protection of major events and emergency response to food service food safety accidents. Organize and implement the health quantitative grading management system for food service units. Supervise and inspect the health management of food service employees. Responsible for guiding the operational work of the Catering Food Supervision Institute. Undertake the Bureau and the Municipal Food Safety Office temporarily assigned the relevant work.

(D) Health Food and Cosmetics Supervision

Implementation of national health food, cosmetics supervision and management of laws, rules and regulations and policies, the formulation of supervision and management of policies, normative documents, draft legislation and supervision and implementation. Undertake the supervision and management of health food, cosmetics health, and organization, guidance and coordination of sub-bureaus to do a good job in the supervision and management of health food, cosmetics within the jurisdiction. Undertake the preliminary examination and record management of health food and cosmetic product registration. Supervise the implementation of health food, cosmetics production, management quality management standards. Organize the implementation of health food, cosmetics safety monitoring and evaluation and its system construction. Responsible for guiding health food, cosmetic review organizations, clean monitoring agency's business. Responsible for health food, cosmetics technical review of the construction and management of the expert database. Undertake the Bureau of temporary work.

(E) Drug Registry

Implementation of national laws, regulations, rules and guidelines on the registration of drugs and related products, the formulation of policies related to supervision and management, regulatory documents, draft legislation and supervision and implementation. It is responsible for the acceptance and examination of applications for registration of medicines, preparations for medical institutions, medicinal excipients, packaging materials and containers in direct contact with medicines, as well as the registration and approval of the above matters undertaken by the provincial food and drug supervision and management departments as stipulated by the state. It is responsible for the application and acceptance review of the protection of traditional Chinese medicine varieties. Responsible for the supervision of drug non-clinical research institutions and drug clinical trial organizations. Responsible for the approval of preparation transfer and use in medical institutions. It is responsible for the formulation (revision) of local standards for Chinese herbal medicines, Chinese medicine preparation standards, preparation standards for medical institutions and other technical standards. Responsible for the implementation of relevant national and local technical standards and technical specifications promulgated. Responsible for guiding the business work of drug testing organizations, drug evaluation organizations, packaging materials and containers in direct contact with drugs testing organizations. Responsible for the recommendation and declaration of national drug and other industry technical review experts, as well as the organization and construction of the city's drug technical review expert database. Responsible for the organization and management of the Bureau's scientific research work. Undertake the Bureau temporarily assigned the relevant work.

(F) Drug Safety Supervision Division

Implementation of national laws, regulations, rules and guidelines on the supervision and management of drug safety policy, the formulation of policies related to the supervision and management, normative documents, draft legislation and supervision and implementation. It is responsible for the supervision and management of drug production and preparation and dispensing, and organizes, guides and coordinates with the branch offices to do a good job in the supervision and management of drug production and preparation and dispensing within the jurisdiction. It is responsible for the work related to the drug classification and management system, and organizes the implementation of the basic drug system in drug production. Organize and implement the monitoring of adverse drug reactions and drug abuse monitoring system. Responsible for drug production, medical institutions, preparation quality management standard certification and supervision and implementation. Responsible for the supervision and management of the production of pharmaceutical stimulants; in accordance with the law to undertake the supervision and management of radiopharmaceuticals, toxic drugs for medical use, narcotic drugs, psychotropic substances and drugs and pharmaceutical chemicals and other special drugs. According to law, it is responsible for matters related to drug production, preparation and formulation, special drugs and other initial filing. It is responsible for the supervision and management of the production and management of packaging materials and containers in direct contact with drugs. It is responsible for the issuance of drug sales certificates. It is responsible for guiding the business work of adverse reaction monitoring organizations, drug abuse monitoring organizations and pharmaceutical cleanliness monitoring organizations. Undertake the Bureau of temporary assignment of the relevant work.

(VII) Medical Devices Supervision

Implementation of national laws, regulations, rules and guidelines for the supervision and management of medical device production, supervision and management of the development of policies, normative documents, draft legislation and supervision and implementation. Responsible for the supervision and management of the production of medical devices, and organizing, guiding and coordinating the sub-bureaus to do a good job in the supervision and management of the production of medical devices under the jurisdiction. Responsible for the production registration of Class I and Class II medical device products and the approval and supervision of clinical trial (validation) of Class II medical devices. Responsible for the supervision and implementation of statutory standards and product classification management of medical device products. Organize and implement the monitoring and re-evaluation of adverse events of medical devices. Organize and implement the quality system assessment of medical device manufacturers, responsible for medical device production quality management standard inspection and supervision and implementation. Responsible for on-site verification of medical device product registration. Responsible for the construction and management of medical device technical review expert database. Responsible for guiding the quality testing of medical devices and product registration and technical review of the organization's business. Responsible for the issuance of "medical device products export sales certificate". Undertake the Bureau of temporary assignment of the relevant work.

(H) Drug Circulation Supervision Division

Implementation of national laws, regulations, rules and guidelines for the supervision and management of the circulation and use of medicines, medical devices and policies, the formulation of supervision and management of policies, regulatory documents, draft legislation and supervision and implementation. Responsible for the supervision and management of the circulation and use of medicines, medical devices, packaging materials and containers in direct contact with medicines, and organizing, guiding and coordinating the supervision and management of the circulation of medicines, medical devices, packaging materials and containers in direct contact with medicines under the jurisdiction of each branch office Responsible for the certification of the quality management standard for pharmaceutical business and supervise the implementation. Organize the implementation of drug circulation, the use of basic drug system, the implementation of drug circulation of prescription drugs and non-prescription drugs classification management system. Collaboration with relevant departments to organize and implement the circulation of drugs, the use of adverse reaction monitoring and drug monitoring system. Cooperate with the relevant departments to organize and implement the circulation of medical equipment, the use of adverse events monitoring. It is responsible for the supervision and management of the circulation and use of pharmaceutical stimulants; it is also responsible for the supervision and management of the circulation and use of special drugs such as radiopharmaceuticals, toxic drugs for medical use, narcotic drugs, psychotropic drugs and drug-type improvised poisonous chemicals, etc. in accordance with the law. It is responsible for the accreditation of drug bidding agencies and drug bidding work. Undertake the work of the Bureau of temporary assignment.

(IX) Integrated Approval Office

Responsible for food service license issuance. Health food production enterprises responsible for health license issuance. Responsible for cosmetic manufacturers of health license issuance. Responsible for drug production license issuance and commissioned production approval. Responsible for radiopharmaceutical production, operation and use of license issuance. Responsible for the issuance of drug business license. It is responsible for the issuance of hospital preparation room license and approval of commissioned preparation of Chinese medicinal preparations. Responsible for the approval of advertisements of drugs, medical devices and health food. Responsible for the issuance of medical device manufacturing license (Class II and III). Responsible for the issuance of medical device business license (Class II and III). Responsible for the Internet drug, medical device information service audit. Narcotic drugs, psychotropic drugs business, transportation, mailing, purchase, carry approval. Responsible for the approval of the purchase license of the first class of drug-type drug-prone chemicals and the filing of overseas commissioned production. Responsible for the approval of export licenses for anabolic agents and peptide hormones, and the filing of overseas commissioned production. It is responsible for the approval of the acquisition and supply units of medical toxic drugs and the approval of the purchase and use of toxic drugs for scientific research and teaching. Responsible for the import of drugs for the record. Responsible for the import of medicinal materials for the record. Organize and carry out the work of license renewal. Undertake the work of the Bureau of temporary assignment.

(J) Planning and Finance

Responsible for the preparation of the budget of the system's budgetary units, the final accounts of the finalization. Responsible for the Bureau of financial management and the management of special funds. Responsible for the bureau system leading cadres of economic responsibility audit and internal audit of the units. Responsible for the organs and affiliated units of the capital construction, state-owned assets management, organization of government procurement related work. It is responsible for the supervision and management of administrative charges and two lines of income and expenditure of the bureau. Responsible for the housing reform of the bureau organs and guiding the housing reform of the subordinate units. Responsible for the logistics and defense work of the Bureau. Undertake the relevant work temporarily assigned by the Bureau.

(XI) Personnel and Education Division (Old Cadre Division)

Responsible for the daily work of the party group of the Bureau. Responsible for division-level leadership team building, division-level leading cadres assessment and day-to-day management. Responsible for division-level reserve cadres selection, training, assessment and management. Undertake the work related to the Bureau's organization, functions and staffing. Responsible for staff recruitment, assessment, rewards and punishments, and daily management. Responsible for staff deployment, labor and welfare management. Responsible for professional and technical titles, talent selection and expert management. Responsible for the political examination and filing of personnel going abroad. Responsible for the organization and management of education and training. Responsible for the registration and management of licensed (from) pharmacists. Responsible for the Bureau of Talent Service Center work guidance. Responsible for the management of retired cadres. Undertake the work of the Bureau of temporary assignment.

(XII) directly under the Party Committee (Bureau of Trade Unions)

Responsible for the Bureau and directly under the unit of the Party's grass-roots organizations, party education and management. Responsible for the bureau and directly under the unit of spiritual civilization construction work, ideological and political propaganda and education. Responsible for the collection, summarization and editing of party affairs information of the bureau and directly subordinate units. Responsible for the work of the Secretariat of the Bureau's Ideological and Political Work Research Association. Responsible for the disciplinary inspection of the Party in the Bureau and the units directly under the Bureau, and undertake the construction of party integrity and anti-corruption work in the Bureau and the units directly under the Bureau. Responsible for guiding the work of the Bureau and directly under the unit of trade unions, *** Youth League, Women's Committee and other mass organizations. Responsible for the bureau organs and units directly under the united front, overseas Chinese Federation, religious work. Assist the Bureau of Personnel Office to do a good job in the Bureau organs and units directly under the management of retired cadres specific work. Responsible for organizing the bureau organs and directly under the unit cadres and workers to participate in politics, the implementation of democratic management, democratic supervision, and actively carry out cultural, artistic and sports activities. Responsible for the construction of trade union organizations and trade union teams, and the training of trade union cadres. Responsible for the collection and use of trade union funds and the management of trade union property. Responsible for family planning and health care work of the bureau organs and directly subordinate units. Undertake the Bureau temporarily assigned the relevant work.

(xiii) Inspection Division (in the city drug supervision and inspection and law enforcement brigade)

Implementation of national laws, regulations, rules and guidelines on drugs, medical devices, health food, cosmetics inspection and law enforcement, the development of policies on inspection and law enforcement, regulatory documents, draft legislation and supervise the implementation. Organize the investigation and handling of drugs, pharmaceutical excipients, packaging materials and containers in direct contact with drugs, medical devices, health food, cosmetics production, circulation, use of major violations of the process. Responsible for the city's drug, medical device, health food, cosmetic sampling plan and organize the implementation; responsible for the city's drug, medical device, health food, cosmetic audit sampling work. Supervising internet drug information service and transaction behavior. It is responsible for the supervision and management of the city's health food, drug and medical device advertisements. Regularly releases information on the quality and safety of the city's medicines, medical devices, health food products and cosmetics and the results of sampling tests. Responsible for the investigation and handling of the city's medicines, medicinal excipients, packaging materials and containers in direct contact with medicines, medical devices, health food products, and cosmetics in major cases. Responsible for the city's drugs, medical devices, health food, cosmetics, complaints, reports of the acceptance of work. Guiding and supervising the inspection and law enforcement, product recall and case investigation of county food and drug supervision and management agencies; coordinating cross-regional supervision and law enforcement work. Undertake the relevant work temporarily assigned by the Bureau.

In accordance with the relevant provisions of the set of disciplinary inspection, monitoring organizations.