1个回答
FDA Guidance for Industry Changes to an Approved NDA or ANDA
该指南第7章
Major Changes (prior Approval Supplement)
Changes that may affect drug product sterility assurance including, where appropriate, process changes for sterile drug substances and sterile packaging components.
Changes to aseptic processing methods, including scale, that extend the total processing, including bulk storage time, by more than 50 percent beyond the validated limits in the approved application.
评论
匿名
提交
取消
匿名
{{item_parent.created_at}}
置顶
批准
驳回
编辑
等待审核
已驳回
回复
{{item_parent.show_reply_list ? '收起回复' : '查看回复'}}({{item_parent.children.length}})
编辑
提交
取消
写回复
匿名
提交
取消
{{item_children.from_user}} 回复 {{item_children.to_user}}
{{item_children.created_at}}
批准
驳回
编辑
等待审核
已驳回
回复
编辑
提交
取消
写回复
匿名
提交
取消
这{{threadTextType}}正{{isAdminText}}
举报
提交
取消
为帮助审核人员更快处理,请填写举报原因:
举报
提交
取消
为帮助审核人员更快处理,请填写举报原因: