药品附条件批准上市申请审评审批工作程序(征求意见稿)

2020-06-01 国家药品监督管理局药品审评中心(CDE) CDE

为配合新修订《药品注册管理办法》的贯彻实施,我中心组织起草了《药品附条件批准上市申请审评审批工作程序(征求意见稿)》,现在中心网站予以公示

中文标题:

药品附条件批准上市申请审评审批工作程序(征求意见稿)

发布日期:

2020-06-01

简要介绍:

为配合新修订《药品注册管理办法》的贯彻实施,我中心组织起草了《药品附条件批准上市申请审评审批工作程序(征求意见稿)》,现在中心网站予以公示

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  1. [GetPortalCommentsPageByObjectIdResponse(id=1072035, encodeId=53ee10e20359a, content=已阅,受益匪浅。, beContent=null, objectType=guider, channel=null, level=null, likeNumber=46, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=6c905475903, createdName=湘雅科教, createdTime=Sat Nov 20 10:04:13 CST 2021, time=2021-11-20, status=1, ipAttribution=)]
    2021-11-20 湘雅科教

    已阅,受益匪浅。

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