Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices
保健产品的灭菌 - 环氧乙烷 - 用于医疗器械灭菌过程的开发 验证和日常控制的要求
发布日期:
2014-07-07
ISO 11135:2014规定了工业和医疗保健设施环境下医疗器械环氧乙烷灭菌过程的开发、验证和常规控制要求,并承认两种应用之间的相似性和差异。
ISO 11135:2014 specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial and health care facility settings, and it acknowledges the similarities and differences between the two applications.