药品上市后变更管理办法(试行)(2021年)

2021-01-12 国家药品监督管理局药品审评中心(CDE) NMPA

为贯彻《药品管理法》有关规定,进一步加强药品上市后变更管理,国家药监局组织制定了《药品上市后变更管理办法(试行)》,现予发布,自发布之日起施行,此前规定与本公告不一致的,以本公告为准。

中文标题:

药品上市后变更管理办法(试行)(2021年)

发布日期:

2021-01-12

简要介绍:

为贯彻《药品管理法》有关规定,进一步加强药品上市后变更管理,国家药监局组织制定了《药品上市后变更管理办法(试行)》,现予发布,自发布之日起施行,此前规定与本公告不一致的,以本公告为准。
  各省级药品监管部门应当落实辖区内药品上市后变更监管责任,细化工作要求,制定工作文件,明确工作时限,药品注册管理和生产监管应当加强配合,互为支撑,确保药品上市后变更监管工作平稳有序开展。
  特此公告。
  
                                                                                                                                             国家药监局
                                                                                                                                         2021年1月12日

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