我国对药品进行监督管理的形式主要有三种:一是企业内部的质量监测;二是群众性的监督管理;三是县以上卫生行政部门代表国家对药品进行监督。《药品管理法》第九章规定:“县级以上卫生行政部门行使药品监督权”,“县级以上卫生行政部门设药品监督员”,“由同级人民政府审核发给证书”。药品监督员有权按照规定对辖区内的药品生产企 There are mainly three forms of supervision and management of pharmaceuticals in China: first, internal quality monitoring; second, mass supervision and management; third, county or higher health administrative departments represent the country to supervise drugs. Chapter 9 of the “Drug Administration Law” stipulates: “Health administrative departments at or above the county level exercise the right to monitor drugs,” “health administrative departments at and above the county level set up drug supervisors,” and “by the same level people’s government to review and issue certificates.” Drug supervisors have the right to comply with regulations for drug production enterprises in their jurisdictions