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作 者:陈蕾[1] 陈英[2] 刘雁鸣 袁耀佐 戴红 涂家生[6] CHEN Lei;CHEN Ying;LIU Yanming;YUAN Yaozuo;DAI Hong;TU Jiasheng(Chinese Pharmacopoeia Commission,Beijing 100061,China;Guangdong Institute for Drug Control,Guangdong 510663,China;Hunan Institute of Drug Testing,Changsha 410001,China;Jiangsu Food and Drug Supervision and Inspection Institute,Nanjing 210008,China;Beijing Institute of Drug Testing,Beijing 100085,China;China Pharmaceutical University,Nanjing 210009,China)
机构地区:[1]国家药典委员会,北京100061 [2]广东省药品检验所,广州510663 [3]湖南省药品检验研究院,长沙410001 [4]江苏省食品药品监督检验研究院,南京210008 [5]北京市药品检验研究院,北京100085 [6]中国药科大学,南京210009
出 处:《中国药品标准》2024年第2期168-175,共8页Drug Standards of China
摘 要:《中国药典》2020年版第一增补本自2024年3月12日起施行,它起着重要的承上启下的作用,其中药用辅料标准新增11个、修订46个。本次制修订药用辅料标准是基于风险管理理念和全过程管理理念,围绕保障药品临床安全性和有效性,在制定标准过程中突出对药用辅料关键质量属性的评估,增加了功能性相关指标、安全性指标,突出了标准国际协调和绿色环保标准理念,加强了标准规范性和可操作性。本文着重介绍了《中国药典》2020年版第一增补本中药用辅料新增和修订标准的总体思路和主要特点。以期对《中国药典》的使用者正确理解、执行或运用药典标准有所帮助。The first supplement of the Pharmacopoeia of the People′s Republic of China 2020 Edition will be implemented on March 12,2024.It plays an important role in connecting link between the preceding and the following.Among them,11 new pharmaceutical excipients monographs have been added and 46 monographs have been revised.This formulation and revision of pharmaceutical excipients standards are based on the concept of risk management and the full lifecycle management and focuse on ensuring the clinical safety and effectiveness of drugs,the evaluation of critical quality attributes on pharmaceutical excipients is highlighted in the standard-making process,and functional-related characteristics(FRCs)and safety indicators are included.Moreover,the excipient standards have emphasized the concept of international pharmacopeia harmonization and green environmental protection and strengthened the standardization and operability.This article focuses on the general framework and the main characteristics of the standards of pharmaceutical excipients in the first supplement of the Chinese Pharmacopoeia 2020,which can contribute to accurately understand and utilize the standards in the Chinese Pharmacopoeia.
关 键 词:中国药典2020年版 第一增补本 药用辅料 标准 解读
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