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NMPA Issued the Guiding Principles for Capacity Building of Medical Device Inspection and Testing Organizations
2019-08-30
NMPA has organized the formulation of and released on August 30,2019 the Guiding Principles for Capacity Building of Medical Device Inspection and Testing Organizations.
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NMPA Issued the Rules for Unique Identification System for Medical Devices
2019-08-27
NMPA has formulated and promulgated on August 27, 2019 the Rules for the Unique Identification System of Medical Devices, which will go into effect as from October 1, 2019.
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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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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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NMPA Issued the Administrative Measures for Drug Quality Sampling Inspection
2019-08-19
NMPA issued the Administrative Measures for Drug Quality Sampling Inspection,effective as of the date of promulgation.