Learn about the investigation, impact and outcome when receiving a positive Biological Indicator in your routine EO Sterilization cycle.

When a positive Biological Indicator is detected during Ethylene Oxide sterilization process, this constitutes a deviation to the requirements of 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).

This Webinar will address the adequate reaction to have in such a situation. A structured investigation method and root cause analysis will be explained and the outcomes will be presented. Speakers will also share practical advice to help prevent or limit the impacts on your business.


Annick Gillet, Director SteriPro consulting (Pharma services)
Nicole Palluck, Consultant, Ethylene Oxide

Click here to view webinar

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