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NMPA issues the Announcement on Adjusting the Relevant Matters Concerning the Definition of the Attributes of Drug/Device Combination Products
CDE releases the List of the Second Batch of Overseas New Drugs Urgently Needed in Clinical Settings
NMPA issues the Announcement on Issues Concerning the Import of Reference Drugs for Clinical Research of Biosimilar Drugs
SAMR issues the Measures for the Administration of Imported Medicinal Materials
Provisions for Post-approval Changes of Drugs (Interim)
Provisions for the Supervision and Administration of Drug Manufacturing
Provisions for Drug Registration
Provisions for Crude Drugs Importation
Good Supply Practice for Drugs
Provisions for Unannounced Inspection of Drugs and Medical Devices (Decree No.14 of China Food and Drug
Provisions for Drug Recall (SFDA Decree No. 29)
Provisions for the Lot Release of Biological Products (CFDA Decree No.39)
Decree of State Food and Drug Administration
NMPA issues the Guiding Principles for Capacity Building of Drug Inspection and Testing Institutions
NMPA issues three informationization standards such as the Basic Technical Requirements for Drug Traceability System
Newly revised drug administration law adopted After deliberation
China revises law to ensure drug safety
NMPA issues the Administrative Measures for Drug Quality Sampling Inspection
Announcement of the National Medical Products Administration, the Ministry of Public Security, and the National Health Commission, on the Inclusion of Varieties including Oxycodone-containing Medicines as Psychotropic Drugs
NMPA issues the Notice on Enabling the New Version of the Drug Production License and other Certificates
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