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The General Administration is publicly soliciting opinions on the 'Draft Revised Regulations on Drug Registration Management'.
Release time:
2017-07-17
The first article is to ensure the safety, effectiveness, and quality control of drugs, standardize drug registration behavior, and formulate these measures in accordance with the "Drug Administration Law of the People's Republic of China" (hereinafter referred to as the "Drug Administration Law"), the "Administrative Licensing Law of the People's Republic of China" (hereinafter referred to as the "Administrative Licensing Law"), the "Implementation Regulations of the Drug Administration Law of the People's Republic of China" (hereinafter referred to as the "Implementation Regulations of the Drug Administration Law"), and the "State Council's Opinions on Reforming the Review and Approval System for Drugs and Medical Devices."
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