摘要
目的提高对药品生产企业的监管水平。方法分析当前药品质量存在的一些共性问题及原因。结果与结论就如何结合药品质量问题加强对药品生产企业的监管进行探讨,提出建议。
Objective To improve the surveillance of pharmaceutical manufacturers in our country.Methods Analyze the main problems of the drug quality and the reasons for them present.Results and Conclusion Put forward some suggestions on how to enhance the surveillance of pharmaceutical mamufactures by think of problems of medivine quality.
出处
《中国药事》
CAS
2011年第5期419-420,423,共3页
Chinese Pharmaceutical Affairs
关键词
药品管理法
药品质量
监督管理
Drug Administration Law of China
drug quality
surveillance