国家药监局:对医疗器械上市後监管风险会持续聚焦产品等整改
国家药品监督管理局医疗器械监督管理司日前召开2021年第一季度医疗器械上市後监管风险会商会时强调,医疗器械上市後监管风险会商应持续聚焦问题、聚焦企业、聚焦产品、聚焦整改,在及时处置发现的风险信号基础上,对产品标准、执法规范、监管制度等提出有针对性的完善意见和措施,进一步完善风险防控机制,不断提升医疗器械质量安全保障水平。
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