本文介绍了2018年医疗器械上市后国家监督管理部门的主要工作,包括不断完善监管法规制度、加大检查力度、加强不良事件监测能力、提升监管基础能力等,分析了当前医疗器械监督管理形势,并对2019年医疗器械监管工作进行了展望,针对医疗器械监管科学化、法治化、国际化和现代化水平提升,提出了相应建议。
<<This article introduces the main work of the medical device post-market supervision done by the national medical device supervision department in 2018,analyzes the current situation of medical device supervision,and prospects the work of medical device supervision in 2019.
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