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作 者:汪祺[1] 于健东[1] 王翀[1] 金红宇[1] 魏锋[1] 马双成[1] WANG Qi;YU Jian-dong;WANG Chong;JIN Hong-yu;WEI Feng;MA Shuang-cheng(National Institutes for Food and Drug Control,Beijing 100050,China)
出 处:《中国现代中药》2024年第4期603-608,共6页Modern Chinese Medicine
基 金:国家重点研发计划项目(2023YFC3504103)。
摘 要:药品抽检是药品监督和执法的重要技术支撑手段,通过分析抽检结果可有效发现上市后药品的质量风险,同时也可评价某类或一定区域内药品的质量。立足于历年国家药品抽检中发现的中成药品种质量问题和潜在安全风险,以与中成药质量相关的原料、生产工艺、辅料及包装材料等环节为切入点,分析已上市中成药需要关注的问题,以期为中成药质量的提升和监管工作的开展提供参考。Drug sampling inspection is an important technical support tool for drug supervision and law enforcement.By analyzing the sampling results,quality risks of post-market drugs can be effectively identified,and the quality of drugs in a certain category or region can also be evaluated.Based on the quality problems and potential safety risks of traditional Chinese patent medicines and simple preparations varieties found in the national drug sampling inspection over the years,this paper aims to analyze the relevant issues that need attention of the listed traditional Chinese patent medicines and simple preparations with the raw materials,production processes,excipients,packaging materials and other links related to the quality of traditional Chinese patent medicines and simple preparations as the starting point,so as to provide a reference for the quality improvement and supervision of traditional Chinese patent medicines and simple preparations.
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