摘要
药用辅料引起的药品使用安全问题频发,加强对药用辅料监管的呼声高涨,通过对加强辅料监管的必要性和可行性进行必要的分析,指出在我国当前不失时机地进行药用辅料的规范化监管是切实可行的。
To analyze the essentiality and feasibility of strengthening the reflection of the pharmaceutical excipients regulation in China,in the context of rising voices as a result of the high frequency of medicinal use of safety issues caused by pharmaceutical excipients.In the meantime to point out it’s feasible to regulate the pharmaceutical excipients by seizing the opportune moment.
关键词
药用辅料
分类
技术审查
备案
pharmaceutical excipients
classification
technical review
to keep on record
