世界中医药
文章摘要
引用本文:张强,王志飞,谢雁鸣,黎元元,王连心,刘峘,耿洪娇,崔鑫,刘福梅,孙春全,魏瑞丽,张利丹.中成药临床综合评价技术规范[J].世界中医药,2021,(22):.  
中成药临床综合评价技术规范
Technical Specification for Clinical Comprehensive Evaluation of Chinese Patent Medicine
投稿时间:2021-10-15  
DOI:10.3969/j.issn.1673-7202.2021.22.024
中文关键词:  中成药  临床综合评价  技术规范  中医药特色  临床定位  临床价值
English Keywords:Chinese patent medicine  Comprehensive clinical evaluation  Technical specifications  Characteristics of traditional Chinese medicine  Clinical positioning  Clinical value
基金项目:国家重点研发计划项目(2018YFC1707400);科技创新工程重大攻关项目(CI2021A00702)
作者单位
张强,王志飞,谢雁鸣,黎元元,王连心,刘峘,耿洪娇,崔鑫,刘福梅,孙春全,魏瑞丽,张利丹 中国中医科学院中医临床基础医学研究所,北京,100700 
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中文摘要:
      药品临床综合评价为药品上市后临床定位、资源配置、医保与基药准入等工作提供了有效的依据。中成药临床综合评价除了满足一般药品综合评价6个维度外,还应考虑中医药特色。目前对于中成药临床综合评价研究的具体实施环节和评价方法比较模糊,因此制定中成药临床综合评价技术规范迫在眉睫。起草组遵循《中国药品综合评价指南参考大纲(第二版)》以及《药品临床综合评价管理指南(2021年版试行)》等文件的相关法规要求,经过文献复习和专家讨论论证,结合多项中成药临床综合评价研究的实践经验,制定了中成药临床综合评价技术规范。本规范包括了中成药临床综合评价的临床定位、资料获取、质量控制、评价内容与方式、各维度的评价技术方法等方面,为中成药开展临床综合评价工作提供方法学指导,使评价过程及结果更加科学合理。
English Summary:
      The comprehensive clinical evaluation of drugs provides an effective basis for the clinical positioning,resource allocation,medical insurance and access of basic drugs.In addition to meeting the six dimensions of general drug comprehensive evaluation,the clinical comprehensive evaluation of Chinese patent medicine should also consider the characteristics of traditional Chinese medicine.At present,the specific implementation links and evaluation methods of clinical comprehensive evaluation of Chinese patent medicine are relatively vague,so it is urgent to formulate the technical specification of clinical comprehensive evaluation of Chinese patent medicine.The drafting group has formulated the technical specifications for clinical comprehensive evaluation of Chinese patent medicines in accordance with the relevant regulatory requirements of the reference outline of the guidelines for comprehensive evaluation of Chinese medicines (Second Edition) and the guidelines for the management of clinical comprehensive evaluation of drugs (trial version in 2021),after literature review,expert discussion and demonstration,and in combination with the practical experience of a number of clinical comprehensive evaluation studies of Chinese patent medicines.This specification covers the clinical positioning,data acquisition,quality control,evaluation contents and methods,evaluation technology and methods of various dimensions of the clinical comprehensive evaluation of Chinese patent medicines,so as to provide methodological guidance for the clinical comprehensive evaluation of Chinese patent medicines and make the evaluation process and results more scientific and reasonable.
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