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of China (SFDA) recently issued GMPs for medical devices are recognized as critical to maintaining quality control Standards(ISO).2 Japan instituted GMP.
Chinese(GB) Contact CFDA REGULATORY GUIDE Drug Administration Law of the People's Republic of China. 4, Regulations for Implementation of the
16 Mar 2011 The State Food and Drug Administration of China (SFDA) published a revised version of the GMP regulation. This new version came into force
21 Mar 2012 The State Food and Drug Administration, P.R. China (SFDA) has of the document is quite similar to the EU GMP Guideline Part I. However,
and Taiwan) Traditional Chinese Medicine and Natural Medicinal Products Notice on GMP certification (for injections, radioactive drugs and biologicals
Chinese GMPs SFDA Good Manufacturing Practice for Drugs (2010 Chinese and English Translation GMPs GMP International Master Reference Guide
Article 1: These provisions of Good Manufacturing Practice (GMP) for Drugs, with the Drug Administration Law of the People's Republic of China and the such as reference standards and reference substances, should be available in
Drug Administration, P.R. China. 2011?4?8????. 1. The Implementation Status and Schedule of. China Drug GMP Supervision. Wang Zhexiong. SFDA
10 Oct 2015 To promote the implementation of the Good Manufacturing Practice for of the inspection results, China Food and Drug Administration (CFDA)
Subsequently, China's State Food and Drug Administra- tion (SFDA) published the staggered implementation plan for GMP 20102 and promulgated several key

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March 2018