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Viscera of US Food and Drug Administration in Guizhou
(1) office.

Responsible for the system construction, comprehensive coordination, supervision and inspection of messages, meetings, confidential documents, confidentiality, statistics, letters and visits, news propaganda, government affairs disclosure, emergency management, comprehensive management and asset management; Guide the information construction of this system; Organize domestic and international exchanges and cooperation related to the supervision and management of food, medicine, health food and cosmetics.

(2) Policy and Regulation Department.

Participate in drafting local laws and government regulations on food and drug supervision and management; To undertake the legality review, coordination and filing of normative documents; To undertake the administrative law enforcement supervision hearing; To undertake relevant administrative reconsideration, administrative litigation and compensation; To undertake the investigation and drafting of major policies related to food and drug supervision and management; To guide the administrative management and legal system construction of food and drug supervision and management institutions in the province.

(3) Food Licensing Office.

To undertake the management of hygiene license for food and cosmetics; To formulate relevant norms and standards for health food, cosmetics and food hygiene licenses in the field of consumption, and supervise their implementation; To undertake the preliminary examination of the use of new raw materials for cosmetics and the production of domestic cosmetics for special purposes according to law.

(4) Food safety supervision department.

Responsible for the supervision and management of food safety in consumption; Formulate safety management standards for food, health food and cosmetics in consumption and supervise their implementation; Organize, implement, supervise and guide the investigation and monitoring of the safety status of food, health food and cosmetics in consumption according to law, and release relevant regulatory information; Review and supervise food and cosmetic advertisements; To guide and supervise the handling of food safety accidents in restaurants, canteens and other consumer areas in the province.

(5) Drug Registration Office (Chinese Medicine and Ethnic Medicine Supervision Office).

To supervise the implementation of national drug standards, Catalogue of Packaging Materials and Containers in Direct Contact with Drugs, standards and registration of pharmaceutical excipients and preparations of medical institutions; Supervise the implementation of quality management standards for drug non-clinical research and drug clinical trials; To organize the implementation of the supervision and management and quality standards of traditional Chinese medicine and ethnic medicine; The implementation of the national Chinese herbal medicine variety protection system and the catalogue of over-the-counter drugs; Organize the formulation and revision of local standards for Chinese medicinal materials (ethnic medicinal materials) and processing specifications for Chinese herbal pieces.

(6) Medical Device Supervision Office.

To undertake the supervision and management of the development, production, circulation and use of medical devices in the whole province; Supervise the implementation of national standards for medical devices; Implementing the catalogue of classified management of medical device products; To undertake the registration and supervision of Class I and Class II medical device products; Supervise the clinical trials of medical devices, the implementation of quality management standards for production and operation, and the certification of production quality system; Supervise the production and operation license of medical devices; Release the quality announcement of medical devices; Review and supervise medical device advertisements; Organize the monitoring, reevaluation and elimination of medical device adverse events; To undertake the supervision and management of Internet information services and transactions of medical devices according to law.

(7) Drug Safety Supervision Office.

Organize the implementation of the national drug classification management system; Participate in the implementation of the national essential drug system; Supervise the implementation of Chinese herbal medicine production, drug production and preparation quality management standards in medical institutions; To undertake the supervision and management of radioactive drugs, narcotic drugs, toxic drugs and psychotropic drugs, pharmaceutical precursor chemicals and drug-induced stimulants; To undertake the supervision of drug production, preparations of medical institutions and other licenses; Organize the monitoring, re-evaluation and elimination of adverse drug reactions.

(8) Drug Market Supervision Office.

To supervise the implementation of the quality management standards for pharmaceutical trading; To be responsible for the supervision and management of drug wholesale and retail chain business license and drug market order according to law; Supervise the implementation of classified management of prescription drugs and over-the-counter drugs; Issue a drug quality announcement; Examining and supervising drug advertisements; To undertake the supervision and management of drug Internet information services and transactions according to law.

(9) Planning and Finance Department.

To be responsible for the declaration, supervision and management of special funds of provincial food and drug supervision departments and national and provincial investment projects; To formulate the financial management system of bureau organs and directly affiliated units and organize their implementation; Comprehensive management of all kinds of funds, property rights and government drug testing equipment procurement; Prepare the department's budget and final accounts, and be responsible for the construction of financial accounting system, fund (asset) management supervision and performance evaluation of the bureau and its subordinate units; To be responsible for the supervision, management and internal audit of administrative fees and incomes from fines and confiscations in the bureau system.

(10) personnel department.

Responsible for the organization, personnel management, labor wages, education and training of the bureau, and guide the above work of the directly affiliated institutions; To formulate the education and training plan, talent team construction plan and rules and regulations of the food and drug supervision system in the whole province, and guide the implementation in conjunction with relevant departments; Implement the qualification accreditation system for licensed pharmacists; Responsible for organizing the evaluation of pharmaceutical professional and technical positions.

Party committees of organs are responsible for the Party-mass work and target management of bureaus and directly affiliated units. Set up the office of the party Committee of the organ.

The office of retired cadres shall be responsible for the work of retired cadres in the bureau and guide the work of retired cadres in directly affiliated units.

The discipline inspection and supervision organization, the Provincial Commission for Discipline Inspection, is stationed in the discipline inspection team of the provincial US Food and Drug Administration, and the provincial supervision office is stationed in the supervision office of the provincial US Food and Drug Administration. There are four administrative staff. Among them, discipline inspection team leader 1 person, and director of supervision office 1 person.