美国药品质量管理由美国卫生部下属的食品药品管理总局(FDA)负责。FDA 的药品局共有工作人员1100人,是仅次于食品局的第二个大局。美国药品管理,主要是根据美国国会通过的法律进行管理的。一、美国药品管理法的沿革主要可分成三个阶段:1906年以前,美国市场上的药品是由欧洲、非洲各国移民带去的各种传统药。国会1906年通过的食品 US drug quality management by the United States Department of Health under the responsibility of the Food and Drug Administration (FDA). FDA’s Drug Administration has a total staff of 1,100 people, is second only to the Food Bureau’s second overall situation. Drug administration in the United States is governed mainly by the law passed by the U.S. Congress. First, the evolution of the U.S. Drug Administration Law can be divided into three main stages: Prior to 1906, the drugs in the United States market were all kinds of traditional medicines brought by immigrants from Europe and Africa. The Diet passed in 1906