阿司匹林肠溶片生物等效性研究指导原则(征求意见稿)

2022-05-02 国家药品监督管理局药品审评中心(CDE) CDE

为不断丰富完善仿制药个药指导原则并持续推进一致性评价工作,进一步规范阿司匹林肠溶片的生物等效性研究,经广泛调研和讨论,我中心组织起草了《阿司匹林肠溶片生物等效性研究指导原则(征求意见稿)》。

中文标题:

阿司匹林肠溶片生物等效性研究指导原则(征求意见稿)

发布日期:

2022-05-02

简要介绍:

为不断丰富完善仿制药个药指导原则并持续推进一致性评价工作,进一步规范阿司匹林肠溶片的生物等效性研究,经广泛调研和讨论,我中心组织起草了《阿司匹林肠溶片生物等效性研究指导原则(征求意见稿)》。

       我们诚挚地欢迎社会各界对征求意见稿提出宝贵意见和建议,以便后续完善。征求意见时限为自发布之日起1个月。

       请将您的反馈意见发到以下联系人的邮箱。

       联系人:李丽;王静

       联系方式:lil@cde.org.cn;wangjing@cde.org.cn

       感谢您的参与和大力支持。

                                                                                                                                                              国家药品监督管理局药品审评中心

                                                                                                                                                                          2022年4月28日

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