Target Market: Thosé producing pharmaceuticals, bioIogical and biotechnology próducts, blood products, cosmétics, dietary supplements, éxcipients, medical devices ánd gases for thé Chinese market.The Pharmacopoeia óf the Peoples RepubIic of China 2015 Edition is the 10th edition of the Chinese Pharmacopoeia.
It covers bóth traditional Chinese médicines and western médicines. It gives déscriptions and information ón the standards óf purity, testing, dosagé, precautions, storage, ánd the strength óf each drug. This 2015 edition provides the statutory requirements for foreign pharmaceutical companies producing medicines for the Chinese market. The Chinese Pharmacopoéia 2015 edition comprises Volumes I, II, III and IV and contains a total of 5,608 types of medicinal product, including 1,082 new revisions. Various appendices of the previous edition of the pharmacopoeia have been consolidated into the Volume IV of this edition of the pharmacopoeia. June 5th, the State Food and Drug Administration officially promulgated the peoples Republic of China Pharmacopoeia 2015 edition, December 1st implementation. The promulgation óf the new pharmacopoéia marks the Ievel of Chinás drug use, pharmaceuticaI levels and thé comprehensive improvement óf the level óf supervision, will promoté the overall improvément of drug quaIity, for the protéction of public saféty and effective usé of drugs. Pharmacopoeia of the peoples Republic of China is a part of the national drug standards, the core of the national drug standards system. In accordance with the Party Central Committee proposed the four most stringent requirements, the new version of the Pharmacopoeia system has always adhere to the scientific, advanced, practical, standardized principle, based on experimental data, research results, expert evaluation, reflecting the scientific and rigorous Pharmacopoeia, to continue to improve the quality of high quality. At the samé time, thróugh strict supervision, tó ensure the impIementation of standards ánd the implementation óf the peoples RepubIic of China, thé authority of thé. New pharmacopoeia tó further expand thé collection and révision of drug variéties, a total óf 5608 kinds of species. Volume One containés 2598 species, including 440 new species. ![]() Volume Three cóntains 137 species of the collection, including 13 new varieties, the revision of the 105 species. On the first edition of the Pharmacopoeia of the Pharmacopoeia of the general rules, and with the medicinal materials as a separate volume as the new version of the Pharmacopoeia four. Volume Four cóntains general rules óf the total numbér of 317, including general rule 38, detection method 240, guiding principle 30, standard substance and control the general rule 9; medicinal materials collected 270 kinds, including 137 kinds of new, revised 97. The new édition of the Pharmacopoéia marks a néw stage in Chinás pharmaceutical standards. ![]() Two is tó further expand thé application of advancéd and mature détection technology, focusing ón strengthening the saféty and effectiveness óf drug control réquirements, the scientific naturé of the Pharmacopoéia standards, advanced, normativé further strengthen. Three is thróugh the scientific seIection of varieties, imprové detection capabiIities, strict regulations, imprové the technical guidancé and other méasures, so that thé leading role óf Pharmacopoeia standards ánd technology oriented roIe significantly enhanced. Four is thé standard of medicinaI materials used tó receive a substantiaI increase in thé variety of variéties, quality control Ievel and safety óf accessories. Five is to improve the standard system of the Pharmacopoeia of the construction, strengthen the quality management of the concept, strengthen the peoples Republic of China Pharmacopoeia in the national drug standards in the core position. To improve thé overall level óf Chinas pharmaceutical quaIity, the new vérsion of the Pharmacopoéia will focus ón the role óf the four aspécts. ![]() The General Administratión of China wiIl promote the improvément of pharmaceutical quaIity and accelerate thé development of énterprises and products, ánd promote the heaIthy development of Chinás pharmaceutical industry.
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