《药品管理法》实施已三周年,我国药品监督管理工作进入了法制化时期.各级卫生行政部门通过进行广泛深入的宣传活动,使《药品管理法》深入人心,药品监督管理体系已初步形成.卫生部及各省、自治区、直辖市制定了相应的实施办法、条例、规定等配套法规.三年执法成绩喜人.通过核发药品生产、经营企业和医院制剂《许可证》,使药品的全面质量管理得到有力的推进.查处假、劣药品,整顿医药市场,打击不法分子的活动,加强了药品监督检验工作.药品生产、经营和使用单位自身管理体制也在改革和健全之中.总之,三年来,以法管药成绩显著,取得了较好的社会 The Third Anniversary of the Implementation of the Drug Administration Law and the Supervision and Management of Drugs in Our Country have entered into a period of legalization. The health administrative departments at all levels have made the “Drug Administration Law” deeply rooted in the public through extensive and extensive publicity activities, and the drug regulatory system has been initially established The Ministry of Health and other provinces, autonomous regions and municipalities have formulated corresponding regulations, rules and regulations and other supporting laws and regulations and achieved satisfactory results in three years through the issuance of “licenses” for pharmaceutical production and operation of enterprises and hospital preparations so that the total quality management of pharmaceutical products Get a vigorous promotion.Check the fake and inferior drugs, rectify the pharmaceutical market, crack down on criminals activities, strengthen drug supervision and inspection work.Pharmaceutical production, management and use of the unit’s own management system is also reform and sound.In short, three years , With a significant result of tube medicine, made a better society