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 国家开放大学 / 医药商品营销实务

按照《中华人民共和国药品管理法》规定,第五十二条:直接接触药品的包装材料和容器,必须符合(    )要求,符合保障人体健康、安全的标准,并由药品监督管理部门在审批药品时一并审批。药品生产企业不得使用未经批准的直接接触药品的包装材料和容器。对不合格的直接接触药品的包装材料和容器,由药品监督管理部门责令停止使用。


A.
药用

B.
储存和运输

C.
国家标准

D.
药品标准
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