医用激光的通知和注意事项说明

Yutaku Kaneta
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引用次数: 0

摘要

在工业界,学术界和政府之间讨论的结果,yakuseikishinhatsu 0629 No. 4“医疗激光申请批准的管理”被通知。新通知不是没有临床试验的规格范围,而是包括激光手术刀在内的医用激光发展指南,主要由非临床评价项目、使用指征和临床试验必要性的基本概念组成。建议咨询药品和医疗器械机构,以决定是否可以仅通过非临床测试评估器械之间的差异。此外,医疗器械上市后的安全措施也很重要,这不是通报的对象,而是审批的审查点之一。尤其需要注意的是,安全管理人员的选择和安全管理区域的设置对于医疗激光的使用至关重要。与产业界、学术界和政府密切合作,不断探讨,对于解决与医用激光相关的临床问题具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Explanation for Notification and Precautions of Medical Laser
In the result of discussions between industry, academia and government, yakuseikishinhatsu 0629 No. 4 ‘Management of medical laser application for approval’ was notified. The new notification shows not the range of specification without clinical trial but the guideline for development of medical laser including laser scalpel, which is mainly composed of non-clinical evaluation items and basic concepts of indication for use and necessity of clinical trial. The consultation with pharmaceuticals and medical devices agency is recommended for the decision that it is possible to evaluate the differences between devices with only non-clinical testing. Additionally, it is important for medical devices to take safety measures for the post marketing, which is not subjected to the notification but one of the review points for approval. Especially, it should be noted that safety manager selection and safety management area setting are essential for medical laser use. It is significant for resolving the clinical problems relative to medical laser to keep discussing continuously and cooperating closely with industry, academia and government.
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