Free Webinar – Be prepared for EO sterilization validation

Why should I join the webinar?

In this webinar, we will:

  • Learn what are the critical parameters of EO sterilization process and what impact they will have on your product safety and performance
  • Go through a detailed checklist that will help you to make the right decisions before you start any EO sterilization validation activities
  • Learn where (and when) it is possible to save time and effort required to validate your medical device according to ISO 11135 and other applicable standards

*At the end of the webinar we will have a quick Q&A session to address your main concerns.

Who should attend?

  • Company or department managers in the medical device field
  • Regulatory affairs and QA experts
  • R&D and and V&V managers
  • Experts involved in the evaluation of Medical Devices and QMS

Keynote speakers:

Sally Bercovich – EO Sterilization Expert, with extensive experience and broad knowledge in different aspects in EO sterilization of medical devices, such as: EO sterilization validations and re-validations, single batch release, change impact assessment, product adoption into validated EO sterilization process risk assessments following re-qualification failure, laboratory testing strategy (microbiology/EO residuals).

Official language: Hebrew


Start Time

5:00 pm

July 1, 2020

Finish Time

6:00 pm

July 1, 2020

Event Participants