摘要
为药品生产企业的清洁验证提供新方法和新思路。通过分析影响清洁效果的因素制定清洗规程草案,使之得到确认。结果表明,优化的、合理的清洁验证是药品生产质量的重要保证。
It was provided some new approaches and avenues for the drug manufacturers during the cleaning validation. By analyzing the factors that affected cleaning efficacy, a cleaning rule draft was work out. Optimal and rational cleaning validation is an important guarantee for quality of drug production.
出处
《中国药事》
CAS
2008年第8期654-656,共3页
Chinese Pharmaceutical Affairs
关键词
药品
清洁
验证
drug
cleaning
validation