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EVENT DATE
Oct 2016
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Reprocessing Medical Devices: Approaches and Considerations for Manual Cleaning Validations

Overview

This webinar will assist medical device designers and manufacturers navigate the reprocessing requirements and successfully execute a manual cleaning validation. This program will present various aspects of manual cleaning validation testing: overall considerations, selection of artificial test soil, soil challenge sites and dwell time, cleaning reagents, manual cleaning techniques, rinse requirements, and acceptance criteria. It will also cover life cycle considerations and challenges in the design of an appropriate validation study.

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