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七月一日是实施“中华人民共和国药品管理法”的一周年。一年来全省医药工商企业在各级政府和卫生、医药主管部门的领导和指导下,围绕贯彻执行“药品管理法”,进行卓有成效的工作。工商企业对照“药品管理法”和“合格证”、“许可证”发放的条件进行了整顿。通过整顿、企业在厂房、设备、人员、工艺、环境、营业场所、仓贮等方面都有不同程度的改善。此外,还对淘汰药品、伪药、劣药、假药和“三无药品”过期变质药品原辅料进行了处理,使医药产品得到了净化。使整个医药行业发生了较大的变化,主要表现在: 1.绝大多数企业质监部门和质检人员,广大职工,真正起到了质量把关的作用,制止
July 1 is the first anniversary of the implementation of the “People’s Republic of China Drug Administration Law.” In the past year, the province’s pharmaceutical industrial and commercial enterprises, under the leadership and guidance of governments at all levels and departments in charge of health and medicine, have conducted fruitful work around the implementation of the Drug Administration Law. The commercial and industrial enterprises rectified the terms of the “Drug Administration Law”, “Certificate of Compliance” and “License” issuance. Through the rectification, enterprises in the plant, equipment, personnel, technology, environment, place of business, warehousing, etc. have varying degrees of improvement. In addition, the phasing out of drugs, counterfeit drugs, substandard drugs, counterfeit drugs and “three non-drug” expired metamorphic drugs raw materials were processed so that the pharmaceutical products have been purified. So that the entire pharmaceutical industry has undergone major changes, mainly in: 1. The vast majority of enterprises quality supervision departments and quality control personnel, the majority of workers, has really played the role of quality control, stop