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药品许可证怎么办理 -法律知识
释义
法律分析:
1.提出申请:向所在地的省级食品药品监督管理局提出筹建申请.递交材料:递交与所申请经营类型相关的材料.材料补正:受理部门根据不同情形进行处理,并告知申请单位补正材料.审核阶段:审核周期为30个工作日.资质发放:对符合条件的单位发放药品经营许可证。从申请到筹建需要一段较长的周期。
法律依据:
《中华人民共和国药品管理法》 第五条 国务院药品监督管理部门主管全国药品监督管理工作。国务院有关部门在各自的职责范围内负责与药品有关的监督管理工作。
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