Linyi USA Food and Drug Administration Viscera

1, organize and coordinate the daily work of the bureau;

2, responsible for bureau messages, meetings, confidential, documents, information, letters and visits, confidentiality, openness of government affairs, supervision, emergency, publicity, information release, administrative reception, logistics services, etc. ;

3. Responsible for drafting comprehensive manuscripts.

(ii) Personnel Section

1, responsible for personnel management and organization of bureau organs and directly affiliated units;

2, to guide the food and drug supervision and management personnel team construction and personnel training;

3, responsible for the implementation of licensed pharmacist qualification system related work;

4. Be responsible for managing the qualification training and management of the counterpart;

5, responsible for the management and service of retirees of bureau organs, and guide the management and service of retirees of units directly under the bureau organs.

(3) Policy and Regulation Section (under the Administrative Licensing Service Section)

1, drafting normative documents on food safety supervision and management of drugs, medical devices, health food, cosmetics and catering services;

2, to undertake the legality audit of normative documents of this Council;

3, responsible for the audit of administrative punishment cases;

4, undertake the relevant administrative reconsideration, administrative litigation, compensation, organization of hearings and other work;

5. To undertake the legal construction of this system; To undertake the centralized handling of administrative licensing (examination and approval) matters of this department.

(4) Planning and Finance Department

1. Draw up the development, construction and equipment planning of food and drug supervision and management and organize its implementation;

2, responsible for the management of special funds for food and drug sampling inspection;

3, responsible for the bureau of financial and state-owned assets management, financial and state-owned assets management guidance bureau organs and directly affiliated units.

(5) Food Safety Supervision Division of Catering Services

1, responsible for the supervision and management of catering service license and food safety in catering service links;

2, organize the implementation of food safety management standards for catering services;

3 responsible for food sampling inspection, food safety investigation and monitoring of catering services;

4. Participate in or organize the investigation of food safety violations in catering services, and investigate and handle food safety accidents in catering services;

5, to guide and coordinate the food safety work of major events.

(6) Health Food Supervision Division

1, responsible for the supervision and management of health food;

2, organize the investigation of health food related violations;

3. Monitor health food advertisements according to law;

4, the issuance of retail enterprises health food business license.

(7) Cosmetics Supervision Division

1, undertake the supervision and management of cosmetics hygiene;

2. Organize to investigate and deal with illegal acts related to cosmetics;

3. Preliminary examination of Cosmetic Hygiene License;

4, supervise the implementation of cosmetic hygiene standards and technical specifications.

(8) Drug Safety Supervision Section

1, organize the implementation of the preparation standards of medical institutions and the processing specifications of Chinese herbal pieces;

2. Supervise the implementation of drugs, auxiliary materials, packaging materials and containers that are in direct contact with drugs, and conduct preliminary examination of preparation registration in medical institutions;

3, supervise the implementation of drug non-clinical research, drug clinical trial quality management norms;

4. Supervise the implementation of the protection system for varieties of traditional Chinese medicine;

5, supervise the implementation of pharmaceutical production and medical institutions preparation quality management standards;

6, undertake the supervision and management of radioactive drugs, narcotic drugs, toxic drugs, psychotropic drugs, pharmaceutical precursor chemicals and other special drugs;

7, to undertake the supervision and management of pharmaceutical production, pharmaceutical preparations and pharmaceutical commissioned production in medical institutions;

8. Responsible for the supervision of drug export;

9. Organize the monitoring of adverse drug reactions.

(9) Drug Market Supervision Section

1, organize the implementation of quality management standards for pharmaceutical trading and certification of pharmaceutical trading enterprises;

2, organize the implementation of drug classification management system in the field of circulation;

3, undertake the supervision and management of drug business license, and issue drug business license for drug retail enterprises;

4, organize the implementation of drug use quality management standards;

5, to undertake the supervision and management of drug information and trading behavior on the Internet;

6. Monitor drug advertisements according to law;

7. Participate in the organization and implementation of the national essential drug system.

(10) Medical Device Supervision Section

1, organize the implementation of management measures and relevant regulations on the production, operation and use of medical devices;

2, supervise the production, management and use quality of medical devices;

3, organize the implementation of medical device standards, undertake the registration of a class of medical device products;

4. To undertake the sampling work of medical device products;

5, supervise the implementation of medical device adverse event monitoring;

6. Monitor medical device advertisements according to law.