药品监督管理是指各级卫生行政部门根据国家有关法律的授权,对行政管理相对人所进行的管理。药品行业管理是指药品生产、经营企业的上级主管部门对其行业内部所进行的管理。二者在国家授权、管理目的、管理依据、管理内容、管理范围、管理职责等方面都有明显的区别,笔者认为,主要表现在如下七个方面。 一、管理性质不同 县以上卫生行政部门根据《中华人民共和国药品管理法》的授权,对药品进行监督管理。《药品管理法》对县以上卫生行政部门做了三 Drug supervision and management refers to the health administrative departments at all levels in accordance with the relevant state laws authorized management of the relative management of the people. Drug industry management refers to the pharmaceutical industry, the higher authorities of their business within the industry management. The two have obvious differences in the aspects of national authorization, management purpose, management basis, management content, management scope, management responsibilities and so on. The author believes that the two are mainly manifested in the following seven aspects. First, the nature of management Health administrative departments at and above the county level in accordance with the “People’s Republic of China Drug Administration Law,” the authorization, supervision and management of drugs. The “Drug Administration Law” made above the county health administrative departments three