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引用本文:袁建龙,林翼旻,黄榕珍,张晓敏,张纾.新法规背景下境内药品再注册的技术审查标准研究[J].中国现代应用药学,2023,40(11):1544-1548.
YUAN Jianlong,LIN Yimin,HUANG Rongzhen,ZHANG Xiaomin,ZHANG Shu.Study on Technical Review Standard of the Re-registration of the Domestic Drugs Under the Background of New Regulations[J].Chin J Mod Appl Pharm(中国现代应用药学),2023,40(11):1544-1548.
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新法规背景下境内药品再注册的技术审查标准研究
袁建龙, 林翼旻, 黄榕珍, 张晓敏, 张纾
福建省药品审评与监测评价中心, 福州 350003
摘要:
目的 构建新药品注册法规背景下境内药品再注册的技术审查标准。方法 通过分析药品法规和审查案例,初步确立境内药品再注册的审查要素,并采用改进德尔菲专家函询法,对33名药品注册审查专家进行2轮函询,统计分析函询结果。结果 制定了一套境内药品再注册的技术审查标准,包括8个一级要素、41个二级要素。结论 本研究构建的技术审查标准有望促进药品再注册技术审查工作的规范化,提升药品再注册技术审查质量。
关键词:  再注册  审查  标准  新法规
DOI:10.13748/j.cnki.issn1007-7693.20220891
分类号:R95
基金项目:福建省药品监督管理局2021年度药品安全监管科研项目(2021001)
Study on Technical Review Standard of the Re-registration of the Domestic Drugs Under the Background of New Regulations
YUAN Jianlong, LIN Yimin, HUANG Rongzhen, ZHANG Xiaomin, ZHANG Shu
Fujian Center for Drug Evaluation and Monitoring, Fuzhou 350003, China
Abstract:
OBJECTIVE To establish technical review standard of the re-registration of the domestic drugs under the background of new regulations. METHODS Through the analysis of drug laws and regulations and review cases, the review elements of the re-registration of the domestic drugs were preliminarily established, and the improved Delphi expert consultation method was used to conduct two rounds of consultation on 33 drug registration review experts, and the consultation results were statistically analyzed. RESULTS A set of technical review criteria for the re-registration of the domestic drugs was developed, including 8 first-level elements and 41 second-level elements.CONCLUSION The technical review standards constructed in this study are expected to promote the standardization of drug re-registration technical review and improve the quality of drug re-registration technical review.
Key words:  re-registration  review  standard  new regulation
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