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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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