EO Sterilization Equipment, Software and Product Validation Per ISO 11135

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  • Published date: October 28, 2020
    • san Jose, california, United States

ISO 11135:2014: “Sterilization of health-care products – Ethylene oxide – Requirements for the development, validation and routine control of a sterilization process for medical devices”, defines the latest requirements for the validation of Ethylene Oxide sterilization of medical devices, the sterilization chamber, and sterilization controls. This webinar will use ISO 11135 as a basis for a field-tested approach to sterilization validation and its documentation, including the chamber control software.

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Ashutos Swain
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