Medical network - August 1, according to sources, the first half of 2017 the national food and drug supervision and administration work symposium ended last week, the meeting summed up the drug supervision for the first half of 2017, with 2017 in the second half of the food and drug supervision work key, the CFDA main leaders made important speech at the meeting. The CFDA should have the following five key priorities in the second half of 2017:
I. strategic upgrading of flight inspection
Daily supervision, inspection and flight inspection will be extended to "food, medicine, medical devices, catering industries... "" production site, business site... "" full process, full range... Closely monitor... The national health industry chain... We will increase the intensity of daily supervision, the intensity of market sampling, the intensity of the punishment of cases and the transparency of the information, and take all the medicine and medicine to ensure the healthy living environment of the people.
Second, drug regulation is not relaxed, food regulation should be strengthened
Full process supervision food source control, food and crops, medicinal herbs, breeding, cultivation, storage and transportation, processing and marketing links, strengthen the multi-sectoral, multi-channel joint operations, security control table, regulation, Chinese medicine yinpian disorderly mess like milk, meat, egg dishes mess... Ensure the people to eat the rest of the security, strictly prevent "disease from the mouth"!
Third, strengthen the supervision system of food medicine
Small make up think, as long as it is related to eat the food of meat and eggs, milk, butter sauce vinegar tea ", "beauty makeup protecting, fresh food, drinks, medicine, health care" products, should be incorporated into the unified, authoritative and professional regulatory system, "the unity of" triad, four market supervision and management system, far cannot satisfy the breadth of a drug regulation, strength, authoritative and professional requirements, regulatory model again, don't know will go?
Iv. Professional and partial functions of the supervisory team "third-party"
The professionalization of the inspector is important, although "occupation" is not necessarily "professional", but professionalization will be a trend. Small make up that inspectors threshold selection that should be set up, preferably in a medicine standing in a line of work for at least 5 years or above, familiar with the pharmaceutical technology, pharmaceutical technology, and pharmaceutical production management, quality management, QC inspection test... In conclusion, we should emphasize the technical expertise and authority of the inspectors. In addition, market sampling inspection, certification inspection, special inspection, meeting training, market research, technical research, laws and regulations, document works... Can be paid to entrust a third party professional organization to do, can mobilize the social forces to participate in many parties, in order to guarantee authority and specialization requirement.
Fifth, we will continue to deepen reform measures
Reform of the examination and approval system for drugs, the system of listed licensee, the evaluation of generic drug consistency, the management reform of clinical experimental institutions... The policies and measures will continue to deepen in the second half of the year, and the food and drug industry chain ecological environment management, the safety management of the big health industry chain... Will further strengthen, the administration of food medicine, a long way!
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