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流感病毒核酸检测试剂注册申报临床研究技术要求探讨
引用本文:李耀华. 流感病毒核酸检测试剂注册申报临床研究技术要求探讨[J]. 中国药物警戒, 2012, 9(6): 340-343
作者姓名:李耀华
作者单位:国家食品药品监督管理局医疗器械技术审评中心,北京,100044
摘    要:本文综合我国流行性感冒病毒既往流行特点、相关法规要求以及获得上市批准的检测试剂等方面内容,探讨流行性感冒病毒核酸检测试剂注册申报时的临床试验设计要求。本文重点阐述了伦理要求、方案设计、参比方法、临床研究单位选择、统计学分析以及临床报告撰写等内容,为此类体外诊断试剂的注册申报提供指导性建议。

关 键 词:流行性感冒病毒  体外诊断  临床试验

Registration Clinical Research Technical Requirements to the Influenza Virus Nucleic Acid Detection Reagents
LI Yao-hua. Registration Clinical Research Technical Requirements to the Influenza Virus Nucleic Acid Detection Reagents[J]. Chinese JOurnal of Pharmacovigilance, 2012, 9(6): 340-343
Authors:LI Yao-hua
Affiliation:LI Yao-hua (Center for Medical Device Evaluation, SFDA, Beijing 100044, China)
Abstract:Based on the characteristic of influenza virus prevalence trend, related regulations and assay reagents, this article illustrated the clinical trial design requirements for influenza vires nucleic acid detection reagent registration. Ethical issues, protocol design, comparative method, study site, statistical analysis and clinical trial report were all involved and provided guidelines for the specific reagent registration.
Keywords:influenza virus  in vitro diagnostic  clinical trial
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