医疗器械注册自检风险管理分析

      Risk Management Analysis of Medical Device Registration Self-inspection

      • 摘要: 通过对涉及注册自检相关法规政策分析,走访调研企业,召开座谈会,以及在全国范围内发放调查问卷的方式,汇总梳理注册自检过程存在的风险,并进行分析、评价。从监管部门和生产企业两个方面,提出完善我国医疗器械注册法规体系,降低各方在注册自检工作中的风险的建议。

         

        Abstract: Through the analysis of laws and policies related to registration self-inspection, visiting and researching enterprises, holding symposiums, and issuing nationwide questionnaires, the risks in the registration self-inspection process were summarized, analyzed, and evaluated. From the aspects of regulatory departments and manufacturing enterprises, we suggest to improve China's medical device registration regulations system and reduce the risks of all parties in the registration self-inspection work.

         

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