摘要
目的促进完善我国医疗机构药品质量的管理规范。方法依据我国现有的药品管理法律、法规,结合医疗机构目前实际的药品管理情况,探讨建立规范我国医疗机构药品管理的方式方法。结果与结论借鉴《药品经营质量管理规范》(GSP)及国内外已有的药品监管经验,可为制订符合我国医疗机构实际情况的药品管理制度提供思路,切实提高医疗机构药品监管的水平。
Objective To perfect the drug quality management standard of the medical institutions in China. Methods According to the existing drug administration laws and regulations as well as the current practical situation of drug management in the medical institu-tions,establish the mode and method of drug management of the medical institutions in China. Results and Conclusion Using the Good Supply Practice（GSP） for Pharmaceutical Products as reference and the existing drug supervision experience at home and abroad to provide the ideas for formulating the drug management system that is,in line with the actual situation of medical institutions in Chi-na,and improve the drug supervision level of the medical institutions.
出处
《中国药业》
CAS
2015年第8期3-4,共2页
China Pharmaceuticals
关键词
医疗机构
药品
质量管理
medical institutions
drug
quality management
