基于医疗器械注册审评流程的风险分析及其对策探讨

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

      • 摘要: 为了加强对医疗器械的监督管理,我国对医疗器械产品实行上市前注册审批制度,其中,技术审评是我国医疗器械注册管理制度中的关键技术环节。以流程为导向,系统梳理了审评流程中各环节存在的风险,并提出风险防范的对策建议,以期强化对审评全过程的质量控制,有效实现审评质量和效率的提升,保障医疗器械审评审批制度各项改革举措落地生效。

         

        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.

         

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