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基于医疗器械注册审评流程的风险分析与对策研究

[Risk Analysis and Countermeasures Investigating Based on Medical Device Registration Review Process].

作者信息

Lan Wengchi, Sun Lei, Fan Rui

机构信息

Center for Medical Device Evaluation, NMPA, Beijing, 100081.

出版信息

Zhongguo Yi Liao Qi Xie Za Zhi. 2020 Apr 8;44(4):334-337. doi: 10.3969/j.issn.1671-7104.2020.04.012.

Abstract

In order to strengthen the supervision and management of medical devices, China implements pre-market registration and approval system for medical device. Technical evaluation is a key point of Chinese medical device registration management system. This study, by process-oriented, systematically sorts out the risks existing in each part of the review process. The countermeasures for risk prevention are proposed, hoping to strengthen the quality control of the whole process of review, improve the quality and efficiency of the review effectively, and ensure the various reform measures of the medical device review and approval system effectively.

摘要

为加强医疗器械监督管理,我国对医疗器械实行上市前注册审批制度。技术审评是我国医疗器械注册管理制度的关键环节。本研究以流程为导向,系统梳理审评流程各环节存在的风险,并提出风险防控对策,以期加强审评全过程质量控制,有效提高审评质量和效率,切实保障医疗器械审评审批制度各项改革举措落地实施。

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