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When Do I Really Need to Perform an Ethylene Oxide Requalification?


One of the first questions that comes to mind after completing an EO sterilization qualification is, "When do I need to perform a requalification study, and what will that study entail?" Maintaining the validated state of a sterilization cycle and ensuring the process consistently and continually...

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One of the first questions that comes to mind after completing an EO sterilization qualification is, "When do I need to perform a requalification study, and what will that study entail?" Maintaining the validated state of a sterilization cycle and ensuring the process consistently and continually delivers the desired SAL is of utmost importance. This presentation takes a comprehensive look at the typical validation approach, the factors that determine when requalification is necessary, and how the expectations in ANSI/AAMI/ISO 11135 have changed in recent years regarding requalification.

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>Duration:30-minutes
>Dates and locations:Available On Demand - July 21, 2016 - July 21, 2018
>Website:http://event.on24.com/r.htm?e=1216096&s=1&k=799D06A1629D671E7A1568109C7F028D&partnerref=QmedProfile
>Hosted by:

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Nelson Laboratories, LLC

http://www.nelsonlabs.com
E: [email protected]
T: (801) 290-7500
F: (801) 290-7998

Address
6280 S. Redwood Rd., Salt Lake City, UT, 84123, United States
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