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中药新药研发与注册过程中的沟通交流
引用本文:韩玲,侯晨晨. 中药新药研发与注册过程中的沟通交流[J]. 中国中药杂志, 2021, 0(3): 730-735
作者姓名:韩玲  侯晨晨
作者单位:国家药品监督管理局药品审评中心
摘    要:近年来,国家药品监督管理局建立了在药品研制和注册过程中的沟通交流机制.该文总结了近年来有关建立药品审评沟通交流制度的改革政策以及具体法规、规章内容,对沟通交流的渠道、流程、方式、类型等进行梳理,并基于临床实践总结、申请临床试验、临床试验期间、上市申请及上市后的再研究等全过程对中药新药沟通交流的现状进行总结,针对目前存在...

关 键 词:沟通交流  中药新药  研发  注册

Communication in process of R&D and registration of new drugs of traditional Chinese medicine
HAN Ling,HOU Chen-chen. Communication in process of R&D and registration of new drugs of traditional Chinese medicine[J]. China Journal of Chinese Materia Medica, 2021, 0(3): 730-735
Authors:HAN Ling  HOU Chen-chen
Affiliation:(Center for Drug Evaluation,National Medical Products Administration,Beijing 100022,China)
Abstract:In recent years,the National Medical Products Administration has established a communication system for the process of drug R&D and registration.In this paper,the reform policies on establishing the communication system for drug evaluation in recent years were summarized,and the channels,processes,methods and types of communication were also collected.In addition,the communication status of new drugs of traditional Chinese medicine(TCM)was summarized according to the whole process of R&D,including summary of clinical practice,Investigational New Drug Applications,period of clinical trials,New Drug Applications,and post-marketing researches.Meanwhile,the current problems such as ineffective,inefficient,repeated or even no communication were analyzed,and relevant suggestions were proposed accordingly in order to provide reference for better communication on R&D and registration of new drugs of TCM.
Keywords:communication  new drugs of traditional Chinese medicine  R&D  registration
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