文章摘要
冯红云,周凌芸,李浩,邵颖,吕心欢,杨建红,左晓春.新药临床试验期间药物警戒和风险控制研究三:药物临床试验期间个例安全性报告监管要求研究[J].中国药事,2022,36(6):630-636
新药临床试验期间药物警戒和风险控制研究三:药物临床试验期间个例安全性报告监管要求研究
Research III on Pharmacovigilance and Risk Control During Clinical Trials of New Drugs: On Regulatory Requirements for Individual Case Safety Reports in Clinical Trials of Drugs
  
DOI:10.16153/j.1002-7777.2022.06.005
中文关键词: 个例安全性报告  临床试验  药物警戒  指导原则  监管要求
英文关键词: individual case safety reports (ICSR)  clinical trials  pharmacovigilance(PV)  guidelines  regulatory requirements
基金项目:
作者单位
冯红云 北京斯丹姆赛尔技术有限责任公司,北京 100045 
周凌芸 赛诺菲(中国)投资有限公司上海分公司,上海 200040 
李浩 康龙化成(成都)临床研究服务有限公司,成都 610041 
邵颖 沈阳药科大学亦弘商学院,北京 100055 
吕心欢 沈阳药科大学亦弘商学院,北京 100055 
杨建红 沈阳药科大学亦弘商学院,北京 100055 
左晓春 沈阳药科大学亦弘商学院,北京 100055 
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中文摘要:
      目的:通过比较分析国内外关于临床试验期间个例安全性报告的相关法规和指导原则要求的异同点,为加强我国药物警戒监管体系中个例安全性报告的监管要求提供理论依据。方法:通过分析ICH、 美国及欧盟临床试验期间个例安全性报告相关的法规以及指导原则情况,与我国相应的监管要求进行比较,研究各国家/地区对试验用药物临床试验期间个例安全性报告监管要求的差异。结果与结论:与其他国家、组织相比,我国已初步建立了临床试验中个例安全性报告快速报告的制度和工作程序,相应的指导原则内容全面,基本涵盖了国际指导原则的核心技术要求,其中基本原则要求一致,但操作细节方面尚缺少详细的指导意见。
英文摘要:
      Objective: By comparing and analyzing the similarities and differences between domestic and foreign regulations and guidelines on individual case safety reports during clinical trials, this research is to provide theoretical references for strengthening the regulatory requirements for individual case safety reports in China's pharmacovigilance regulatory system. Methods: The regulations and guildlines for individual case safety reports during clinical trials in ICH, the United States and European Union were analyzed and compared with the relevant regulatory requirements in China. The diff erences of regulatory requirements for individual case safety reports in various countries/regions during clinical trials of investigational drugs were studied. Results and Conclusion: Compared with other countries and organizations, our country has preliminarily established the regulations of rapid reporting of individual case safety reports during clinical trials and the working procedures. The corresponding guiding principles are comprehensive in content and basically meet the core technical requirements of the international guidlines, of which the basic principles and core technical requirements are consistent, but there is still a lack of detailed guidlines in terms of specifi c operations.
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