摘要
目的促进药用辅料监管,确保药品安全,对药用辅料监管工作提出建议。方法对目前国内药用辅料生产、使用、监管情况进行总结,对存在的问题进行分析。结果与结论对药用辅料监管工作,应在法律法规、管理体系、标准建设等多方面予以加强。
Objective To improve the administration of pharmaceutical excipients and ensure the medication safety,the relative suggestions were provided.Methods The manufacturing,using and administration of pharmaceutical excipient in china were reviewed,and problems existed in pharmaceutical excipients administration was analyzed.Results and Conclusion To enhance the excipients administration,more effort focus on enacting of laws and regulations,improving of management mechanism,construction of quality control system should be made.
出处
《中国药事》
CAS
2011年第1期5-7,共3页
Chinese Pharmaceutical Affairs
关键词
药用辅料
监管
建议
pharmaceutical excipients
administration
suggestion
