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SFDA Spells Out Tasks For 2009

This article was originally published in PharmAsia News

Executive Summary

China's State FDA will concentrate on improving the regulation of standards and supervision of food and drugs in 2009, with the aim of raising standards for all drugs marketed within five years. The agency will speed up its action plan by strengthening international cooperation on formulating standards; revising or raising the quality level of 2,000 drugs; and revising the 2010 Chinese Pharmacopoeia edition. In addition, SFDA will finish the revision of Regulations for the Supervision and Administration of Medical Devices; conduct research on revising the Drug Administration Law and Regulations for the Hygiene Supervision on Cosmetics; implement Provisions for Drug Registration and its complementary documents; as well as continuously formulate and standardize technical appraisal guidelines for drugs and medical devices. (Click here for more - Chinese Language)



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