Policy & News
Management of Adverse Drug Reaction Reporting and Monitoring
2023-04-27
Article 1 In order to strengthen the post-market supervision of medicines, standardise the reporting and monitoring of adverse drug reactions, control the risks of medicines in a timely and effective manner, and safeguard the safety of medicines for the public, these Measures are formulated on the basis of the Drug Administration Law of the People's Republic of China and other relevant laws and regulations.
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