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六届全国人大常委会第七次会议通过了《中华人民共和国药品管理法》(简称《药品管理法》),标志着我国药品管理进入了新的阶段。自从1985年7月1日实施以来,我省卫生等部门在各级党委和政府的领导下,通过广泛开展宣传,加强监督监测队伍建设,进行医药市场综合治理,严厉打击制售假劣药品活动等。使药政执法在困难和挑战面前,创业起步。力求发展,初步形成了依法管药的可喜局面。
The seventh session of the Standing Committee of the National People’s Congress of the Sixth National People’s Congress passed the “People’s Republic of China Drug Administration Law” (referred to as “Drug Administration Law”), marking that China’s drug administration has entered a new stage. Since its implementation on July 1, 1985, the provincial health and other departments under the leadership of party committees and governments at all levels have carried out extensive publicity, strengthened supervision and monitoring of team construction, conducted comprehensive management of the pharmaceutical market, and severely cracked down on the production and sale of counterfeit and inferior pharmaceutical activities. Wait. To make drug administration law enforcement start in the face of difficulties and challenges. In order to develop, we have initially formed a gratifying situation in administering drugs according to law.