1985年7月1日起施行的《中华人民共和国药品管理法》第一章总则第一条规定:“为加强药品质量监督,保证药品质量,增进药品疗效,保障人民用药安全,维护人民身体健康,特制定本法”。将保证药品质量作为法律的形式肯定下来,其意义是非常重大的。药品质量的好坏影响药品的疗效和人民用药的安全,也就直接影响人民的健康。 July 1, 1985 came into effect “People’s Republic of China Drug Administration Law,” Chapter I General Provisions of the first chapter: “In order to strengthen drug quality supervision, to ensure drug quality, enhance the efficacy of drugs to protect people’s drug safety and safeguarding people’s health , Specially formulated this law. ” The significance of ensuring the quality of medicines as a form of law is very significant. The quality of the drug affects the efficacy of drugs and the safety of people’s medication, which directly affects people’s health.