Strengthen supervision of Chinese medicine and folk medicine to promote industrial development - medicine - pharmaceutical industries
August 27, 2010 version of "Chinese Pharmacopoeia" preparation work is completed, the amendments focused on solving the long- Chinese Herbal Medicine And less commonly used pharmaceutical excipients national standards, low quality control issues, and formed a Chinese herbal medicine, Chinese Herbal Medicine Traditional Chinese medicine, chemicals, medical supplies, biological products such as a full range of standard system of medicine, basic coverage National Essential Drug List of species.
Previous day, the state, "Chinese National Standards and Testing Centre for Drugs" was proclaimed, "to improve quality standards and strengthen quality control, to strengthen supervision of Chinese medicine and folk medicine, and promote industrial development" is the Chinese National Standards and Testing Centre for Drugs clear development goals.
New Pharmacopoeia: covering variety of essential medicines "National Essential Drug mostly wide variety of clinical applications, the 2010 version of" Chinese Pharmacopoeia "first with the national essential medicines containing the aim is to make it more secure, better reflect the standard of services for the supervision, regulation of public service concept. "National Pharmacopoeia Committee Deputy Secretary-General Zhou Fucheng told reporters that the 2010 version of" Chinese Pharmacopoeia "failed to receive the national essential medicines containing varieties, the National Pharmacopoeia Committee will give priority to" be added to the Chinese Pharmacopoeia "in the closing set.
It is understood that the standard of medicine in China mainly by the "Chinese Pharmacopoeia", Department of (Board) issued standards for Chinese herbal medicines and provincial registration standards and norms etc. Pieces Processing, national drug standard formulation and revision of drug supervision and management by the State Council Administration Organization Pharmacopoeia Committee. "Chinese Pharmacopoeia" compiled since 1953 1st edition published 2010, edition of "Chinese Pharmacopoeia" is the new China was founded in the ninth edition of the Pharmacopoeia. "Chinese Pharmacopoeia" is the core of our standard system drugs, is drug research, production, management, use and supervision of the statutory basis. "Adhere to standards to improve product quality standards and advanced the principle of production for many of the same species, standard-setting on high not to low, the Chinese pharmaceutical standards in safety and quality control in terms of gradual integration with the international advanced standards, is 2010 version of "Chinese Pharmacopoeia" from the beginning to formulate a clear purpose. "Zhoufu Cheng stressed. According to Zhou Fucheng
introduced new pharmacopoeia will be divided into traditional Chinese medicine, chemical drugs, biological products, 3, was formally published in early 2010, July 1, 2010 from the Executive.
It is reported that, compared with the 2005 edition of Pharmacopoeia, Pharmacopoeia add new varieties of a total of 1358, the total to 4615. Upgrading the technological content, the new collection contains extensive pharmacopoeia advanced technology and sophisticated detection method. In order to strengthen the control of drug safety, new pharmacopoeia also improved drug safety testing of common technical requirements, new guiding principles of the microbe, stepped up heavy metals and harmful elements, impurities, residual solvent control.
On August 27 Pharmacopoeia Committee of the Ninth held an enlarged meeting of the Executive Committee, the State Food And Drug Administration Shao Mingli stressed that the standard drugs is a national medical technology, industrial development and comprehensive reflection of the level of drug administration. No relative standard pharmaceutical research and registration work order, there can be a high level of national drug standards.
Shao pointed out that in recent years, great efforts to carry out the State Board for Registration of Pharmaceuticals for disclosure of information on-site verification, approval number concentration of species identification and review of the transition period, in order to improve the national drug standards laid a solid foundation. In encouraging innovation, the National Council promulgated the "Provisions on the Administration drug registration special approval" for the development of new medicines to provide more services. Recently published "Drug transfer registration regulations" to allow new drugs, listed drugs and imported drugs for many years under certain conditions, technology transfer, aimed at leading pharmaceutical companies to reduce a simple change in dosage form and Generic Goods declaration number, approval number the reasonable control of the total; used to control risk, reduce the blind change formulations, imitation may be the risk, while reducing duplication and homogenization of low-level, the promotion of pharmaceutical production specialization and the concentration of upgrade.
Shao Mingli said that to establish the most stringent pharmaceutical standards, in 2008 the state finance allocated 100 million yuan of special funds specifically for the national drug standards improved, investment in this area this year will reach 190 million yuan.
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