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《中华人民共和国药品管理法》的颁布与实施,标志着我国的药品管理进入了“以法管药”的法制化管理的新阶段,也使我国的药政管理工作进入了全面整顿和全面建设的新时期.药品作为一种特殊商品,其质量优劣和使用是否得当,直接关系着人民用药的安全有效.然而,当前在药品的生产、供销和使用等方面还存在不少问题:①有意制售假劣药案件不断出现;②不经审查批准非法制造药品的情况时有发生;③违令销用淘汰药品的情况曾相当严
The promulgation and implementation of the “Drug Administration Law of the People’s Republic of China” symbolized that our country’s drug administration entered a new stage of legalized administration of “administering drugs by law” and also brought the administration of drug administration in our country into an overall rectification and overall construction The new period of medicine.As a special commodity, the quality and use of medicine is directly related to the safety and effectiveness of people’s medication.However, there are still many problems in the aspects of drug production, supply and marketing, The production and sale of counterfeit drugs continued to occur; ② The situation of illicit drug manufacture has been violated without examination and approval; ③ The case of drug obsolescence has been severely punished