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The State Food and Drug Administration has identified six major tasks for 2010
Time:2019-01-21

In 2010, the National Food and Drug Administration Work Conference and the Party Style and Clean Government Construction Work Conference were held. Vice Premier Li Keqiang made important instructions. Director Shao Mingli made a work report from January 18 to 19, 2010 National Food and Drug Supervision Work Conference and Party Style and Clean Government Construction Work. The meeting was held in Beijing.
The Party Central Committee and the State Council attach great importance to food and drug supervision. On January 15, Li Keqiang, member of the Standing Committee of the Political Bureau of the CPC Central Committee and Vice Premier of the State Council, made important instructions on the opening of the meeting. Li Keqiang said that in 2009, the national food and drug supervision system conscientiously implemented the central decision-making and deployment, actively promoted the reform of the medical and health system, and achieved remarkable results in supervision and institutional reforms, especially in the areas of prevention and control, and improvement of food and drug safety. An important contribution. I would like to express my sincere greetings and heartfelt thanks to the cadres and staff of the whole system! In the new year, food and drug supervision faces new opportunities and challenges. It is hoped that the food and drug supervision system will thoroughly implement the scientific development concept, practice the scientific supervision concept, focus on promoting the key work of medical reform, and accelerate the establishment of a new food and drug supervision mechanism and safety responsibility. System, fully perform functions, strengthen supervision capabilities, and make new contributions to safeguarding the health and safety of the people and improving the quality of life!
In the work report to the General Assembly, Director Shao Mingli guided the scientific concept of development as a guide, comprehensively reviewed and summarized the remarkable achievements of the food and drug supervision work in 2009 in eight aspects, scientifically analyzed the opportunities and challenges faced by the current supervision, and proposed The main ideas of the supervision work in 2010 have clarified the six major tasks and requirements, and emphasized the persistence of the implementation of the scientific development concept and the comprehensive strengthening of the supervision team.
Shao Mingli pointed out that 2009 is the most difficult year for China's economic development since the new century. It is also the year in which the food and drug supervision work is the most complicated and the most difficult task for reform. All system cadres and workers are facing difficulties and actively carry out in-depth study and practice of scientific development concept activities; go all out to ensure the quality and safety of A-stream prevention and control drugs; solidly promote the special rectification of drug safety; actively explore the implementation of catering services, health food and cosmetics supervision New responsibilities; efforts to strengthen the construction of laws, regulations and standards; vigorously strengthen the supervision of basic drug quality; comprehensively improve the ability of food and drug supervision; earnestly grasp the party's work style and clean government construction and other eight aspects have achieved remarkable results.
Shao Mingli pointed out that this year is a crucial year for advancing the reform of the medical and health system. It is an important year for the provincial food and drug regulatory agencies to fully implement their new functions and the comprehensive reform of the municipal and county-level institutions. Doing a good job this year is of great significance to consolidating the basis of food and drug supervision, ensuring the safety of the public's diet and medicine, and promoting coordinated economic and social development. According to the overall thinking of the food and drug supervision work in 2010, Shao Mingli proposed to adhere to the principle of paying more attention to grassroots development, paying more attention to infrastructure construction, paying more attention to administration according to law, paying more attention to technical support, paying more attention to mechanism innovation, and paying more attention to the implementation of responsibility.
Shao Mingli proposed to focus on the following six aspects of work this year:
First, focusing on strengthening the construction of city and county regulatory agencies, we will further promote the reform of the food and drug regulatory system. It is necessary to speed up the establishment of work mechanisms such as team management, funding guarantee, law enforcement supervision and responsibility implementation in line with regulatory tasks.
Second, focus on ensuring the quality and safety of essential drugs, and conscientiously do a good job in the reform of the medical and health system. On the basis of comprehensively strengthening the supervision and control of the production and operation of essential drugs, we will focus on the following four tasks: First, comprehensively improve and improve the quality standards of 307 essential drugs. The second is to implement a comprehensive sampling test and conduct targeted evaluation tests. The third is to launch the national electronic drug catalogue of all kinds of national essential drug catalogues nationwide. This year, all kinds of antimicrobial drugs and injections should be included in the electronic supervision network. The fourth is to improve the city-level drug adverse reaction monitoring, reporting and evaluation system, and carry out quality monitoring pilots in production, distribution and use.
The third is to focus on improving the long-term mechanism and carry out in-depth rectification of drug safety. This year, the special rectification of drug safety should be greater, the pace should be faster, the measures should be more realistic, and new breakthroughs must be made in the construction of long-term mechanisms. It is necessary to strengthen departmental linkage. More progress will be made in combating the production and sale of counterfeit and inferior drugs, rectifying advertisements for illegal drugs, rectifying non-pharmaceutical counterfeit drugs, and organizing investigations into major cases.
Fourth, focus on improving the standardization level and effectively strengthen the daily supervision of medical devices. This year we will continue to lay the foundation and grasp the norms. First, we must speed up the revision and implementation of the Regulations on the Supervision and Administration of Medical Devices and related supporting regulatory documents, so that the supervision of medical devices is more standardized and more scientific. Second, we must effectively strengthen the registration and approval of medical devices. Strengthen the management of medical device standards, improve the review and approval procedures, and improve the efficiency of technical review. Third, we must do a good job in the implementation of medical device GMP. Strengthen the supervision of key regulatory catalogue products and continuously improve product quality. Fourth, we must strengthen the monitoring report and re-evaluation of medical device adverse events. Properly handle adverse events, seriously investigate and deal with quality accidents, and ensure the quality and safety of medical devices.
Fifth, focusing on strengthening infrastructure, and actively fulfilling new duties such as catering services, health food, and cosmetics supervision. The supervision of catering services, health foods and cosmetics is still in its infancy. The main tasks of this year are to lay a solid foundation, strengthen supervision, deepen rectification and enhance capabilities. We must speed up the system construction. Accelerate the construction of laws and regulations in accordance with the requirements of the Food Safety Law and its implementation regulations; accelerate the improvement of capabilities. Strive for local support and ensure that the supervision team is in place; deepen safety and rectification. Increase the rectification of school canteens, canteens in construction sites, and unlicensed business catering activities, and severely crack down on illegal addition of non-edible substances, abuse of food additives, and illegal addition of drugs to health foods. Comprehensively carry out the work of clearing and recertifying health food. At the same time, it is necessary to start food safety evaluation work and demonstration project construction for catering services, and promote local government to strengthen food safety supervision of catering services.
Sixth, focusing on improving supervision capabilities, earnestly do a good job in the preparation of the 12th Five-Year Plan. All localities should put the "Twelfth Five-Year Plan" on the important agenda and put it into the overall plan of local social and economic development. By 2020, China will build a well-off society in an all-round way. We must clearly define the staged goals for food and drug regulatory capacity in the next five years. It is necessary to strengthen the construction of technical support systems such as intensive standard management, inspection and testing, review and approval, inspection and certification, monitoring and evaluation, and risk assessment, and strengthen the construction of supervision informationization in a more prominent position. It is necessary to focus on improving grassroots law enforcement conditions and improving the quality of grassroots teams, and pay more attention to the construction of city and county supervision capacity.

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