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GLP法规下医疗器械生物学试验的实施要点
引用本文:王雪,张旻,宋捷,王欣,胡燕平,李波,王军志. GLP法规下医疗器械生物学试验的实施要点[J]. 中国药事, 2010, 24(9): 860-863
作者姓名:王雪  张旻  宋捷  王欣  胡燕平  李波  王军志
作者单位:中国药品生物制品检定所,国家药物安全评价监测中心,北京,100176
摘    要:
目的论述GLP法规下医疗器械生物学试验的实施要点。为我国推行医疗器械GLP以及为从事医疗器械检测检验的实验人员提供参考。方法介绍医疗器械生物学试验的特点、生物学评价的原则及生物学试验的实施要点。结果与结论医疗器械生物学试验应根据其材料和用途等特征选择合适的试验方法,依据风险评价、风险-利益分析、GLP及重新评价等原则进行安全性评价。

关 键 词:医疗器械  GLP  生物学试验

Points to Consider on Biological Tests of Medical Devices under GLP Regulation
Wang Xue,Zhang Min,Song Jie,Wang Xin,Hu Yanping,Li Bo,Wang Junzhi. Points to Consider on Biological Tests of Medical Devices under GLP Regulation[J]. Chinese Pharmaceutical Affairs, 2010, 24(9): 860-863
Authors:Wang Xue  Zhang Min  Song Jie  Wang Xin  Hu Yanping  Li Bo  Wang Junzhi
Affiliation:(National Center for Safety Evaluation of Drugs,National Institute for the Control of Pharmaceutical and Biological Products,Beijing 100176)
Abstract:
Objective The important points to perform the biological evaluation of medical devices under GLP are discussed.To promote the medical device GLP to be carried out and provide reference for the medical device evaluation personnel. Methods Introducing the characters of biological test,principle of biological evaluation as well as important points to perform biological evaluation. Results and Conclusion Medical device should be evaluated by suitable biological test according to the character of material and use under a series of principles,such as risk analysis,risk-benefit analysis,GLP and re-evaluation.
Keywords:GLP
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