Official the price of virtual high drug prices low picture quality and avoid new network security – vidalia

Official: the price of virtual high price low quality and avoid the shadow ring the amount of security – Beijing, Beijing, November 7, according to the Ministry website news, the Ministry and other six departments recently jointly issued the "guidelines for the pharmaceutical industry development plan". The guide put forward, establishment of market leading drug price formation mechanism, strengthen the convergence of price policy and insurance, procurement, medication and other policies, in the suppression of high prices at the same time, to avoid the influence of low price supply and quality safety. Guide pointed out that the "12th Five-Year" period, China scale pharmaceutical industry scale rapid growth, innovation capacity significantly improved, continue to strengthen quality management, technology and equipment of a substantial upgrade, restructuring and integration of rapid development, to accelerate the pace of internationalization. The guidelines also pointed out, but there are still some problems in pharmaceutical industry, mainly in: the original innovation ability, the ability of basic research and translational research is weak, high quality innovation; product quality upgrading is urgent and generics, Chinese herbal medicine and traditional Chinese medicine, medical equipment, accessories package material quality standards and quality etc. to improve the level of drug supply security; there is a short board, cheap drugs, drugs for children and a rare disease drug shortage problems still occur. Guidelines establish market leading drug price formation mechanism, strengthen the convergence of price policy and insurance, procurement, medication and other policies, in the suppression of high prices at the same time, to avoid the influence of low price supply and quality safety. We will improve the policy of classified procurement of drugs, set up the evaluation criteria of bidding procurement scientifically, improve the quality evaluation methods, and promote the survival of the fittest. The guidelines put forward, standardize and promote the high value of medical supplies sunshine procurement, improve the allocation of large medical equipment and medical service price policy, promote the use of new medical devices in accordance with the provisions of timely access to clinical use. Scientific and rational development and adjustment of basic medical insurance payment standards, and promote the reform of Medicare payment methods to promote rational drug use. According to the ability to bear the health insurance fund, will meet the conditions of innovative drugs in accordance with the provisions of the health insurance directory. Vigorously develop commercial health insurance to meet the diverse and multi-level health needs. Guidelines proposed to strengthen the supervision of drug and medical device laws and regulations system, the revision of the People’s Republic of China drug management law, improve the top-level management of drug design. We will actively promote the reform of the examination and approval system for pharmaceutical and medical devices, and strictly control the approval of the market for over supply and low levels of repetitive products, and speed up the examination and approval of innovative drugs and medical devices that are in urgent need of clinical use. Perfect method, technical specification and efficacy of generics quality consistency evaluation, through the packaging and labeling, hospital procurement, Medicare payments, technical renovation and other support policies, encourage and guide enterprises to carry out the consistency of the evaluation. This guide, strengthen international pharmaceutical inspection cooperation, accelerate the pace of international mutual recognition GMP. Perfect number transfer, commissioned the production and cross regional construction supervision policy, to promote mergers and acquisitions and integration of resources, reduce duplication and idle capacity. The implementation of the most stringent standards, the most stringent regulation, the most severe punishment, the most serious accountability requirements, strengthen supervision and inspection, to promote the implementation of a unified encoding drug, establish traceability body covering the whole process of drug production and circulation.相关的主题文章: