摘要
目的:考察制剂配制设备清洁规程的可靠性。方法:采用最终淋洗水法取样分析。结果:呋喃西林残留量及微生物检查均符合限度标准。结论:制剂配制设备的清洁规程是安全、可靠的。
Objective ： To observe the reliability of cleaning procedure for preparation equipment. Methods： The final water washing method was used to conduct sampling analysis. Results：The residue of furacilin and microbe examination are complying with the standard. Conclusion ： Cleaning procedure for preparation equipment establised by our hospital is both safe and reliable.
出处
《抗感染药学》
2008年第1期24-25,35,共3页
Anti-infection Pharmacy
关键词
制剂
清洁
验证
preparation
clean
validation
