Ningbo Food And Drug Administration

Obligation

I. Implement the state and provincial laws, statutes and regulations on the supervision of food, health products, cosmetics, medicine and medical appliance; in conjunction with relevant departments, work out the local regulations and rules on the safety management of food, health products, and cosmetics when entrusted; being entrusted to draft the local regulations and rules on the supervision of the medicine and medical appliance; Make supervision policies and working plans on food, health products and cosmetics, and the normative documents of the medicine supervision.

II. Exercise the authority to supervise the safety management of food, health products and cosmetics; Organize and coordinate the safety management of food, health products and cosmetics undertaken by the relevant departments.

III. Organize to carry out the investigation and disposal on the serious safety accidents of food, health products and cosmetics in accordance with the law; make the supervision over the safety of food, health products and cosmetics in the county; organize and assist the relevant department to conduct the rescue operation of serious safety accidents of food, health products and cosmetics.

IV. Coordinate the safety testing and assessment of food, health products and cosmetics, instruct and coordinate the establishment of the food safety testing and assessment system; collaborate with relevant departments to make the methods of analyzing, forecasting and issuing the safety information of food, health products and cosmetics and supervise the implementation; issue the information regularly.

V. Implement the market access standard of health products; supervise and implement quality rules of the health products and conduct the examination of advertisements of the health food; supervise the sampling inspection of the health products; responsible for the relevant work of health products licensing.

VI. Supervise the implementation of the legal standard of drugs, the packing material and container of drugs; implement the classification and administrative protection system of drugs, protect the varieties of traditional Chinese medicine.

VII. Supervise the implementation of the legal standard for medical biology material and medical appliance products, and products classification management catalogue; issue the registration certificate of the first class medical appliance after being approved, responsible for the registration of the manufacturing and business of the first class medical appliance, and supervise the implementation of the standard for the registered products; conduct the quality system for medical appliance and supervise the implementation of the quality rules; be entrusted to inspect the manufacturing and business operation of the medical appliance; make market supervision over the medical appliance.

VIII. Supervise the implementation of management regulations for drug non-clinic research and clinic trial and quality rules for drug producing, business operation and preparations from medical institution; issue the business license to the drug retailers according to the law.

IX. Inspect the quality of drugs and medical appliance from drug manufacturers and medical institution; supervise the implementation of the purchase and sales rules on prescription drugs, OTC drugs, raw traditional Chinese medicinal materials and traditional medicine prepared in ready-to-use forms; supervise the trading of traditional Chinese medicinal material in city and township market and the operational agencies in the district established by the drug and medical appliance manufacturers and business operators; inspect and punish the act and person liable concerning the marketing and sale of fake or bad quality medicine or medical appliance.

X. Supervise the application of narcotics, psychotropic drugs, poisonous substances, drug-breaking medicine, radioactivity drugs and special medical appliance; supervise the implementation of testing rules of adverse reaction of drugs and medical appliance; inspect the advertisement for drugs, medical appliance and health products.

XI. Implement qualification system, registration and administration for licensed pharmacists; conduct training for relevant personnel; organize technical position assessment of medical profession and conduct vocational qualifications admittance system.

XII. Perform the duties in the Management Rules of Medicine Importing, responsible for keeping records for the medicine importing in the Ningbo port.

XIII. Collaborate with the macro-control department to implement the state industry policy of food and drug; organize drug supervision and the foreign exchange and cooperation on the safety management of food, health products and cosmetics

XIV. Direct and administer the local food and drug administrative intuitions and bureau intuitions.

XV. Undertake other issues delivered by the municipality and superior Food and Drug Administration; undertake the routine work of Ningbo Food Safety Commission.