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《药品管理法》于1985年起施行。这标志着我国的药品管理已经走上了法制的轨道。5年来,我们通过学习贯彻《药品管理法》,不断改变药品制剂的小生产规模,提高药品生产的法制观念,出现了层层抓管理,人人重质量,年年有进步的新局面。1989年,遵照国家卫生部发布的《药品生产质量管理规范》(GMP)的要求,对制剂室进行了技术改造,补充了部分制剂设备和药检设备。同时还抽调技术骨干,重新审定了操作规程,整顿了制剂品种,制定了《制剂管理细则》,总后卫生部于1989年6月28日在我院召开了旧制剂室改造现场学术报告会。在1989年全军制剂质量检查评比中,获全军十二佳制剂单位之一。
The Drug Administration Law came into force in 1985. This indicates that our country’s drug administration has embarked on the track of legal system. In the past five years, through studying and implementing the “Drug Administration Law”, we have continuously changed the small-scale production scale of pharmaceutical preparations and improved the legal system concept of pharmaceutical production. We have seen a new situation in which management at all levels and people are all over the top quality and are progressing year after year. In 1989, in accordance with the requirements of the “Good Manufacturing Practices for Pharmaceutical Production” (GMP) issued by the Ministry of Health of the People’s Republic of China, technical modifications were made to the preparation room to supplement part of the preparation equipment and drug testing equipment. At the same time also deployed the backbone of the technology, re-examined the operating procedures, reorganized the varieties of preparations, formulated a “preparation management rules”, the General Ministry of Health on June 28, 1989 held in our hospital old preparation room reconstruction site academic report. In 1989 the whole army preparation quality inspection appraisal, by the army one of 12 best preparation units.