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    EO Sterilization Equipment, Software and Product Validation Per ISO 11135

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    Website | Edit Freely


    Deadline: November 08, 2020 | Date: November 18, 2020

    Venue/Country: U.S.A

    Updated: 2020-10-05 15:44:59 (GMT+9)

    Call For Papers - CFP

    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.

    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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