《中华人民共和国药品管理法》,定于今年7月1日正式施行。这是我国药政历史上由国家颁布的第一部药政法规,标志着我国药政管理工作进入了法制化的新阶段。国家制订《药品管理法》的目的,就是要把国家有关药品监督的方针、政策和原则用国家法律的形式确定下来,把药品的质量置于国家和广大人民群众的严格监督之下,使卫生、医药、工商、公安、司法等部门在药政管理工作中都有章可循,有法可依。这对促进药品生产、保证药品质量、提高药品疗效、保护社会生产力和我军战斗力,将起重大的作用。军队 “People’s Republic of China Drug Administration Law”, scheduled for July 1 this year, the official. This is the first medical and pharmaceutical law and order promulgated by the state in the history of the pharmaceutical administration in our country, which symbolizes that our country’s pharmaceutical administration has entered a new stage of legalization. The purpose of the formulation of the “Drug Administration Law” by the state is to determine the guidelines, policies and principles of the state concerning drug supervision in the form of state laws and place the quality of the drugs under the strict supervision of the state and the broad masses of the people so that health The departments of medicine, industry and commerce, public security and judicial administration all have rules and regulations in the administration of drug administration and there is law to follow. This will play a significant role in promoting the production of medicines, ensuring the quality of medicines, improving the curative effect of medicines, and protecting the social productive forces and the combat effectiveness of our army. army