State Food and Drug Administration issued an opinion to promote food and drug production opera-adobe gamma

The State Food and Drug Administration issued opinions   to promote the food and drug production operators to improve the traceability system, people.com.cn Health Channel – people.com.cn original title: to promote the food and drug production operators to improve the traceability system according to the "food safety law" and the "Drug Administration Law" and "medical equipment supervision and management regulations" "cosmetic health supervision regulations" and other relevant laws regulations and the "Office of the State Council on accelerating the important product traceability system construction opinions" spirit of the document, recently, the State Food and Drug Administration issued to promote the food and drug production operators to improve food and drug traceability system views. Opinions requirements, food traceability system is an important part of food and drug production and management of quality and safety management system. The food and drug production operator shall assume the main responsibility for the construction of the traceability system of food and drug products, realize the source to be investigated, the destination can be traced. In case of quality and safety problems, timely recall related products, search the reasons. Food production operators shall, in accordance with relevant laws and regulations of the raw material purchase, production process, product inspection and sales to record, ensure data authenticity, accuracy, integrity and traceability. In principle, food producers and operators should use information technology to establish traceability system. Do not have the conditions of production operators, can use paper records, such as traceability. The duration of the paper record shall be carried out in accordance with the relevant provisions of the food safety law. Pharmaceutical and medical device manufacturing enterprises shall record the activities in accordance with their production quality management standards (GMP). Records shall be true, accurate, complete and traceable. To encourage pharmaceutical and medical device manufacturers to assign a unique identifier to the smallest sales unit of the product so that the operators and consumers. An implantable medical device shall mark the manufacturer’s name or trademark, batch code (lot number) or serial number to ensure traceability. Pharmaceutical and medical device operating enterprises shall record the activities in accordance with the requirements of the management quality control standards (GSP). Records shall be true, accurate and complete and can be traced back to ensure that medicines and medical equipment purchase, maintenance, warehousing, transportation and other aspects of traceability, and according to the provisions of the use of computer information management system for effective management. Drugs and medical devices used should be in accordance with the "measures of drug supervision and management of medical institutions (Trial)" and the "measures" the quality supervision and management of the use of medical devices of medicines and medical equipment purchase, acceptance, storage and use of records. Cosmetics production enterprises shall be in accordance with the provisions of relevant laws and regulations of "cosmetic health supervision regulations", to ensure production and quality control activities can be traced, and record the products to enter the circulation of the flow of information, realize the product, can check the whereabouts of timely recall. Cosmetics producers and traders should focus on imported cosmetics, domestic special purpose cosmetics, children’s cosmetics and other high-risk products, to promote the construction of traceability system. Opinions, the local food and drug supervision departments in accordance with the "food safety law" the "Drug Administration Law" and "medical equipment supervision and management regulations" "cosmetic health supervision regulations" and other relevant laws and regulations, supervision and Administration)相关的主题文章: