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 SFDA solicits opinions on Implementation Measures for Special Approval Procedures for Drug Registration (interim) (2007-10-09)
 SFDA specifies relevant issues concerning the implementation of newly-revised Provisions for Drug Registration (2007-09-29)
 SFDA solicits opinions on application form for drug registration and instructions on the filling (2007-09-29)
 SFDA solicits opinions on Requirements for On-site Verification and On-site Inspection for Drug Registration (draft for comments) (2007-09-29)
 Comments solicitation on the Regulations for Supervision and Administration of Medical Devices (revised draft) (2007-09-27)
 National "safe medication of drugs, ensured security of human lives" publicity month started (2007-09-26)
 SFDA issues the No.119 announcement of drug administrative protection (2007-09-25)
 SFDA solicits opinions on Provisions for Drug Recall (draft for comments) (2007-09-20)
 SFDA solicits opinions on Supplementary Requirements for the Registration of TCM (draft for comments) (2007-09-18)
 The Financial Times' Interview with SFDA Commissioner Shao Mingli (2007-09-14)
 SFDA to hold 2007 Pharmaceutical Intellectual Property Rights Forum  (2007-09-12)
 SFDA issues the No.118 announcement of drug administrative protection  (2007-09-10)
 SFDA issues six working procedures including Procedure for Re-issuance of Medical Device Registration Certificate  (2007-09-05)
 Chinese vice premier stresses international pharmaceutical co-op  (2007-09-03)
 SFDA holds conference on intensifying food safety special rectification (2007-08-29)
 SFDA requires intensifying the supervision of drug retail business (2007-08-21)
 SFDA solicits opinions on Requirements for Determining Health Food Testing Institutions  (2007-08-14)
 SFDA solicits opinions on Provisions for Implementation of the Special Regulations of the State Council on Intensifying Safety Control of Food and Other Products (2007-08-14)
 Shao Mingli emphasizes intensifying supervision and administration to ensure Olympic food and drug safety (2007-08-13)
 Standard Registration Procedure for Domestic Class III Medical Devices and Overseas Medical Devices put into practice (2007-07-30)
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