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药品是医疗、预防、计划生育的物质基础.加强对药品的监督管理,是为了保障人民群众用药的安全和有效.药品监督管理工作作为卫生事业的组成部分,在我国,经历了曲折的发展过程.随着《药品管理法》的颁布实施,赋予了法定性质和科学的、全面的监督管理内涵.经过一年多来的初步实践,一个新的药品监督保证体系的概念,在人们的思想认识中已基本成型.为了实现在“七五”期间建立健全这个体系,特就目前药品监督管理工作的形势和改革任务,提出以下意见.
Drugs are the material basis for medical treatment, prevention and family planning, and the supervision and administration of drugs are strengthened in order to ensure the safety and effectiveness of drug use by the public. As an integral part of health care, drug supervision and management work has undergone a tortuous course of development in our country With the promulgation and implementation of the Drug Administration Law, the connotation of statutory nature and scientific and comprehensive supervision and management has been given.After more than a year of initial practice, a new concept of drug supervision and assurance system has been put forward in people’s minds In order to achieve the establishment and perfection of this system during the “Seventh Five-Year Plan”, we hereby put forward the following opinions especially on the current situation of drug supervision and management and the task of reform.