Abstract
Purpose of Review
This review aimed to introduce the regulations management and current situations of drug safety evaluation in China.
Recent Findings
The nationwide implementation of good laboratory practice and good clinical practice guarantees the quality of pre-marketing drug safety evaluation. In recent years, post-marketing drug safety monitoring is changing from passive mode to the combination of active and passive monitoring. A national adverse drug reaction monitoring sentinel alliance has been created to actively identify, report, and evaluate adverse reactions, with more than 1.4 million cases reported in 2017. But the quality of the reports is not optimal, with few reports from drug manufacturers, low rate of severe reports, and trend of lag reporting.
Summary
Drug safety evaluation in China is transitioning from passive monitoring to a combination mode. Drug pharmacovigilance is a powerful tool for active monitoring, but participation by drug manufacturers would be essential to an effective drug safety evaluation system.
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Acknowledgments
We thank DONG Jiangping (chief pharmacist, Center for Food and Drug Inspection of National Medical Products Administration), DONG Duo (chief pharmacist, National Center for Adverse Drug Reaction Monitoring, China), and HUO Yan (research fellow, National Institutes for Food and Drug Control) for their great help in revising this manuscript.
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Li, L., Yin, J. Drug Safety Evaluation in China. Curr Allergy Asthma Rep 19, 39 (2019). https://doi.org/10.1007/s11882-019-0872-4
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DOI: https://doi.org/10.1007/s11882-019-0872-4