Responsible for the daily operation of the organs such as messages, meetings, confidential information, archives, supervision, finance, administrative fees and fixed assets management. Undertake the work of openness, security, statistics, letters and visits, and draft important manuscripts.
(2) Food Safety Comprehensive Coordination Office.
To undertake the daily work of the Office of the Provincial Food Safety Committee, as well as the assessment and evaluation of the relevant departments and the Municipal People's Government in performing their duties of food safety supervision and management. Undertake food safety statistics, analyze and predict the overall situation of food safety, and organize food safety risk early warning and risk exchange. Participate in the formulation and implementation of food safety risk monitoring implementation plan.
(3) Department of Policies, Regulations and Science and Technology Standards.
Organize the drafting of local laws and regulations on food and drug supervision and management, undertake the review of normative documents and administrative punishment cases, and undertake administrative law enforcement supervision, administrative reconsideration, administrative litigation and hearing. Organize the implementation of major scientific and technological projects in food and drug supervision and management, and promote the food and drug inspection and testing system, electronic supervision traceability system and information construction. Supervise the implementation of qualification certification conditions and inspection specifications of food and drug inspection and testing institutions. Participate in the formulation of local food safety standards.
(4) Food production supervision department.
Grasp and analyze the food safety situation and problems existing in the production process, put forward suggestions on improving the system and mechanism and work, handle food production licenses in strict accordance with the conditions and procedures stipulated by laws and regulations and bear corresponding responsibilities, and urge lower-level administrative organs to strictly implement administrative licenses according to law, perform supervision and management responsibilities, and timely discover and correct illegal and improper behaviors.
(5) Food Circulation Supervision Office.
Grasp and analyze the food safety situation and existing problems in circulation, put forward suggestions on perfecting the system and mechanism and improving the work, and urge the lower administrative organs to strictly implement the administrative license according to law, fulfill their supervision and management responsibilities, and timely discover and correct illegal and improper behaviors.
(6) Food and Catering Supervision Office.
Grasp and analyze the food safety situation and existing problems in catering consumption, put forward suggestions on perfecting the system and mechanism and improving the work, and urge the lower administrative organs to strictly implement the administrative license according to law, fulfill their supervision and management responsibilities, and timely discover and correct illegal and improper behaviors.
(7) Administration of drug registration.
In strict accordance with the conditions and procedures prescribed by laws and regulations, handle the registration of drugs, preparations of medical institutions, pharmaceutical excipients with national standards, packaging materials and container products that are in direct contact with drugs, and assume corresponding responsibilities, optimize the registration management process, supervise the implementation of non-clinical research of drugs, quality management norms for clinical trials of drugs, and processing norms for Chinese herbal pieces, and organize the implementation of the variety protection system for Chinese medicines.
(8) Drug production supervision office.
Grasp and analyze the situation and existing problems of drug production safety, and put forward suggestions on perfecting the system and mechanism and improving the work. In strict accordance with the conditions and procedures prescribed by laws and regulations, handle the licensing of drug production and preparations in medical institutions and bear corresponding responsibilities, and urge lower-level administrative organs to perform their supervision and management responsibilities in strict accordance with the law, and timely discover and correct illegal and improper behaviors. To undertake the supervision and management of radioactive drugs, narcotic drugs, toxic drugs, psychotropic drugs and pharmaceutical precursor chemicals. Organize the monitoring and re-evaluation of adverse drug reactions.
(9) Drug Circulation Supervision Office.
Grasp and analyze the safety situation and existing problems of drug circulation, put forward suggestions on improving the system, mechanism and work, handle the drug business license in strict accordance with the conditions and procedures stipulated by laws and regulations and bear corresponding responsibilities, and participate in the bidding supervision of drugs (including basic drugs and medical devices). Supervise and urge the lower administrative organs to strictly implement administrative licenses and fulfill their supervisory and management responsibilities in accordance with the law, and timely discover and correct illegal and improper behaviors.
(10) Medical Device Supervision Office.
Grasp and analyze the safety status and existing problems of medical devices, put forward suggestions on improving the system, mechanism and work, handle the registration, production and business license of medical devices in strict accordance with the conditions and procedures stipulated by laws and regulations, and assume corresponding responsibilities, and supervise the implementation of medical device quality management norms. Supervise and urge the lower administrative organs to perform their duties of supervision and management in strict accordance with the law, and timely discover and correct illegal and improper behaviors. Organize the monitoring and re-evaluation of medical device adverse events.
(eleven) health food and cosmetics supervision department.
Grasp and analyze the safety status and existing problems of health food and cosmetics, put forward suggestions on improving the system and mechanism, handle the administrative licensing of health food and cosmetics in strict accordance with the conditions and procedures stipulated by laws and regulations, and bear corresponding responsibilities. Supervise and urge the lower administrative organs to perform their duties of supervision and management in strict accordance with the law, and timely discover and correct illegal and improper behaviors. Organize the monitoring and re-evaluation of adverse events of health food and cosmetics.
(12) Inspection Bureau.
Organize and investigate major food and drug safety violations, guide and supervise local inspections, standardize administrative law enforcement, and promote the improvement of the linkage mechanism between administrative law enforcement and criminal justice. Formulate and organize the implementation of the relevant product supervision and sampling plan in the province. Supervise the recall and disposal of defective products. To undertake the examination and guidance of advertisements for drugs, medical devices and health foods.
(13) Emergency Management and Publicity Division.
Promote the construction of food and drug safety emergency system, organize the preparation of emergency plans and carry out drills, undertake emergency handling and investigation of major food and drug safety accidents, and guide and coordinate the emergency handling of local food and drug safety incidents. Supervise the implementation of the unified announcement system of food and drug safety information, and undertake the work of food and drug safety science popularization and news information release.
Personnel and Education Department (Foreign Exchange and Cooperation Department).
To undertake personnel management, institutional setup, team building and training of organs and directly affiliated units. Responsible for the registration of licensed pharmacists and organizing the evaluation of pharmaceutical (pharmaceutical) professional technical titles. Organize foreign exchanges and cooperation in food and drug supervision and management.
(15) Planning and Financial Audit Bureau.
Formulate food and drug safety plans and organize their implementation. To undertake budget and final accounts, finance and auditing, and supervise and manage state-owned assets.
Party committees of government organs are responsible for the party-mass work of government organs and units directly under Ningxia.
The office of retired cadres shall be responsible for the work of retired cadres in the organs and guide the work of retired cadres in directly affiliated units.
Provincial drug inspection office
Jiangsu Food and Drug Inspection Institute (Jiangsu Food Inspection and Testing Center) is a technical organization that conducts technical supervision and inspection of food and drug quality under the leadership of the US Food and Drug Administration in Jiangsu Province. Its main duties are to be responsible for drug quality supervision and inspection and technical arbitration, drug registration inspection, import drug inspection, drafting and revision of national drug standards, and to carry out scientific research and business technical guidance on drug inspection; To undertake sampling inspection, food quality evaluation and arbitration inspection of comprehensive food safety supervision in the province, and provide diagnostic basis for sudden food safety incidents.
Sheng medical equipment inspection office
Jiangsu Medical Device Inspection Institute specializes in registration inspection, market supervision inspection, entrusted inspection and quality arbitration inspection of medical device products (quasi-production/trial production) and packaging products, and is engaged in relevant technical training and business guidance and consultation.
Provincial drug certification center
1, entrusted by the provincial US Food and Drug Administration, to conduct technical review of pharmaceutical production enterprises, business enterprises and preparation rooms of medical institutions applying for certification, and organize on-site inspection of certification; Assist in the preliminary examination of drug research institutions and clinical trial bases applying for acceptance; Participate in the inspection of post-certification supervision.
2, entrusted by the provincial drug administration, undertake the technical review of medical device product registration information and organize the technical review; Participate in the on-site inspection of medical device production quality system review.
3, undertake the province's adverse drug reactions, medical device adverse events monitoring and drug abuse monitoring; Carry out re-evaluation of drugs after listing.
4, entrusted by the provincial drug administration, undertake the technical review of the original data of new drug declaration, and participate in the on-site review of the reporting unit.
5, entrusted by the provincial drug administration, organize technical review and on-site review of the application materials of medical institutions.
6, undertake the daily management of drug certification inspectors, quality system internal auditors and related experts; Good manufacturing practice (GMP), good manufacturing practice (GSP), good manufacturing practice (GLP), good manufacturing practice (GLP), good manufacturing practice (GAP) and good manufacturing practice (GUP) will be organized jointly with the provincial drug supervision and training center.
7, according to the arrangement of the provincial drug administration, to carry out academic exchanges and cooperation with relevant institutions at home and abroad, to carry out related technical consultation and other work.
8. To undertake other tasks assigned by the Provincial Bureau.
Provincial Adverse Drug Reaction Monitoring Center
(a) to undertake the collection, management and reporting of adverse drug reaction data in the province (including medical devices, the same below), and to provide professional guidance to the professional institutions of adverse drug reaction monitoring in cities and counties (cities, districts).
(two) to undertake the construction, operation and maintenance of the adverse drug reaction monitoring information network in the province.
(3) Organizing education and training on adverse drug reactions.
(4) Organizing international exchanges and cooperation in the field of adverse drug reaction monitoring.
(5) Organizing the research on monitoring methods of adverse drug reactions.
(six) to undertake other tasks entrusted by the US Food and Drug Administration.
(VII) Organize and coordinate the monitoring of adverse reactions of key varieties, carry out post-marketing drug re-evaluation, release adverse reaction monitoring information, and provide professional adverse reaction consultation for drug-related units and the public according to the relevant arrangements of the State Food and Drug Administration and the Provincial Food and Drug Administration.
Provincial pharmaceutical association
Jiangsu Pharmaceutical Society, formerly known as Nanjing Pharmaceutical Society, was separated from Nanjing Pharmaceutical Society in 1962 and established Jiangsu Pharmaceutical Society (known as Jiangsu Branch of China Pharmaceutical Society), which is an academic group composed of medical scientific and technological workers with intermediate titles or above or equivalent education engaged in pharmaceutical management, pharmaceutical education, pharmaceutical research, hospital pharmacy, pharmaceutical production and pharmaceutical management in our province.
Xuzhou Medical Higher Vocational School
The school belongs to Jiangsu American Food and Drug Administration. It is the only provincial medical vocational college in Jiangsu Province. It is a national and provincial training base for biopharmaceutical technical skills named by the Ministry of Education and the Provincial Department of Education.