摘要
A/B级洁净区的动态监测数据为产品的风险评估、最终放行提供了强有力的依据,保证了患者的用药安全。综述了A/B级洁净区生产过程动态监测的意义、作用、项目内容、方法和注意点。
The dynamic monitoring data A / Class B clean areas of risk assessment products and ultimately release provides a strong basis to ensure the safety of the patient＇s medication. A / B grade clean area production process summarized the significance of dynamic monitoring role, project content, methods, and pay attention.
出处
《科技与创新》
2015年第4期87-88,共2页
Science and Technology & Innovation
关键词
GMP
A/B级洁净区
无菌制剂
动态监测
GMP
A / B grade clean area
sterile preparations
dynamic monitoring
