医疗器械注册质量管理体系现场核查指南(征求意见稿)

2020-08-04 国家药品监督管理局(NMPA) NMPA

为进一步加强医疗器械注册质量管理体系核查工作,提升医疗器械注册管理工作水平,国家药监局组织起草了《医疗器械注册质量管理体系现场核查指南(征求意见稿)》(见附件)

中文标题:

医疗器械注册质量管理体系现场核查指南(征求意见稿)

发布日期:

2020-08-04

简要介绍:

为进一步加强医疗器械注册质量管理体系核查工作,提升医疗器械注册管理工作水平,国家药监局组织起草了《医疗器械注册质量管理体系现场核查指南(征求意见稿)》(见附件)

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