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NMPA Issued Three Informationization Standards such as the Basic Technical Requirements for Drug Traceability System
2019-08-27
NMPA has issued three informationization standards such as the basic technical requirements for drug traceability system.
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NMPA Issued the Guiding Principles for Capacity Building of Drug Inspection and Testing Institutions
2019-08-30
NMPA has organized the formulation of and released on August 30,2019 the Guiding Principles for Capacity Building of Drug Inspection and Testing Institutions.
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Newly Revised Drug Administration Law Adopted After Deliberation —To Comprehensively Implement the Four Strictest Requirements and Effectively Protect Drug Safety for the Public
2019-08-26
The remarkable results of pharmaceutical reforms and effective practices were transformed into laws to beef up rule of law for public health.
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Provisions for In-vitro Diagnostic Reagent Registration (Abolished)
2019-07-25
The Provisions for In-vitro Diagnostic Reagent Registration, adopted at the executive meeting of China Food and Drug Administration on June 27, 2014, is hereby promulgated and shall be effective as of October 1, 2014.
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Provisions for Supervision of Drug Distribution
2019-07-25
The Provisions for Supervision of Drug Distribution, adopted at the executive meeting of the State Food and Drug Administration on December 8, 2006, is hereby promulgated and shall go into effect as of May 1, 2007.
