(1) Office (Planning and Finance Department).

Responsible for the daily operation of messages, meetings, confidential documents, archives and other organs, as well as security, government affairs disclosure, letters and visits, publicity, finance and other work, and guide the system information construction; Manage the transfer payment special funds and project funds and supervise the implementation; To undertake the supervision and management of administrative fees; Responsible for personnel, education, organization and asset management of organs and subordinate units; To be responsible for the work of retired cadres in organs and guide the management of retired cadres in subordinate units.

(2) Policy and Regulation Department.

To undertake the supervision of administrative law enforcement; Participate in the drafting of laws and regulations related to food and drug supervision and management; To undertake relevant administrative reconsideration, administrative litigation and hearing.

(3) Food Licensing Office.

To undertake the management of hygiene license for food and cosmetics; Responsible for accepting applications for health food registration; Undertake the preliminary examination of sanitary conditions of domestic cosmetics; Responsible for the management of health food and cosmetics hygiene license.

(4) Food safety supervision department.

To undertake the supervision and management of food safety in consumption links and supervise the implementation of food safety management norms in consumption links; To undertake the investigation and monitoring of food safety in consumption links and release relevant information on food safety supervision in consumption links; Undertake cosmetic safety evaluation according to law; To undertake the hygiene supervision and management of health food and cosmetics.

(5) Chinese medicine and ethnic medicine registration and supervision departments.

Supervise the implementation of national drug standards, Catalogue of Packaging Materials and Containers in Direct Contact with Drugs, and medical requirements and standards; Responsible for the preliminary registration of drugs, protected varieties of traditional Chinese medicine, packaging materials and container products that are in direct contact with drugs; Responsible for the registration and examination of preparations and pharmaceutical excipients in medical institutions; Responsible for the re-registration of drugs and preparations in medical institutions; Guide the research and development of Tibetan medicine and the establishment of quality standard system; Supervise the implementation of the catalogue of over-the-counter drugs and the quality management standards for drug clinical trials; Organize the implementation of the national medicine protection system.

(6) Department of Drug Safety Supervision (Department of Medical Device Supervision).

To supervise the implementation of quality management standards for pharmaceutical production, preparations in medical institutions and Chinese herbal pieces; To undertake the supervision and management of radioactive drugs, narcotic drugs, toxic drugs, psychotropic drugs and pharmaceutical precursor chemicals; To guide the monitoring of adverse drug reactions and drug abuse; Participate in the formulation of provincial essential drugs list; To undertake the production and operation license of medical devices, the safety supervision of medical devices and the registration and filing of Class I medical devices; Supervise the implementation of the national standards for medical devices and the classified management catalogue of medical device products, and undertake the registration, supervision and management of the second class medical devices; Supervise the implementation of quality management standards for clinical trials, production and operation of medical devices; Organize the testing of medical devices and the monitoring of adverse events.

(7) Inspection Institute (Drug Circulation Supervision Institute).

Organize the supervision and inspection of drugs and medical devices, and investigate and deal with major illegal cases of drugs, medical devices, health food and cosmetics according to law; Guide and coordinate the inspection work in the whole province; Organize emergency handling of emergencies; Formulate supervision and sampling inspection plans for drugs and medical devices and organize their implementation, and issue quality announcements; Supervise the advertisements of drugs, medical devices, health foods and cosmetics; Guide, supervise and inspect law enforcement, emergency management, advertising management, product recall and case investigation; To undertake the issuance and management of licenses for pharmaceutical wholesale enterprises; To undertake the daily supervision of drug circulation and use; To undertake the classified management of prescription drugs and over-the-counter drugs in the circulation field.