摘要
以美国思泰瑞(STERIS)公司的常温汽化过氧化氢(VHP)灭菌系统为例,探讨了VHP灭菌系统在新版GMP下生物制品无菌转运中的优势性及必要性。
Exampled with VHP room temperature sterilization system produced by STERIS,in this article,the necessity of using VHP sterilization system in transportation of biological products under sterilization condition required in new edition of GMP and its advantages were discussed.
出处
《医药工程设计》
2011年第3期12-14,共3页
Pharmaceutical Engineering Design
关键词
VHP
新版GMP
无菌转运
VHP
new edition of GMP
Aseptic transportation
