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A comparison study of Taiwan regulation and GHTF regulatory model on in vitro diagnostic medical devices

机译:台湾监管与GHTF监管模型对体外诊断医疗器械的比较研究

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摘要

Introduction: In Taiwan, In Vitro Diagnostic Medical Device (IVD) is regulated as medical device since 1987, and the implementation of IVD registration was fully completed in 2005. The management system of IVD medical device is highly similar with a guidance The GHTF Regulatory Model' developed by Global Harmonization Task Force (GHTF) in 2011 for use of regulation development on medical devices.Area covered: In this study, the Regulatory Model developed by GHTF was compared with Taiwanese IVD management system and it has shown that these two regulatory frameworks are highly similar.Expert commentary: The experience of IVD management in Taiwan can serve a strong evidence to prove the feasibility and effectiveness of GHTF Regulatory Model.
机译:简介:在台湾,自1987年以来,在台湾诊断医疗器械(IVD)被调节为医疗器械,并于2005年完全完成了IVD注册的实施。IVD医疗器械管理系统与GHTF监管模型的指导高度相似 “由2011年全球协调工作组(GHTF)制定用于使用监管制定的医疗设备。涉及:在本研究中,GHTF开发的监管模式与台湾IVD管理系统进行了比较,并表明这两个监管框架 高度相似.Expert评论:台湾IVD管理的经验可以提供强大的证据来证明GHTF监管模式的可行性和有效性。

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