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DAY 2: Validating, Optimizing and Monitoring EO Sterilization Processes

Published Date: February 25, 2021

Establishing an EO sterilization process can be a complicated path as multiple factors play a role in the design of a successful validation: adequate product characterization to determine an appropriate monitor device, definition of process parameters that are adequate for the product and sterilization load, and the definition of the validation activities to verify adequacy. Selecting the right validation approach would reduce the need for future cycle optimization to address things like the reduction of EO usage, reduction in product residuals, reduction in cycle times or the development of an appropriate process for parametric release. The validation approach selected can also facilitate (or complicate) annual validation and process review and/or prequalification.

During this 2-part webinar, attendees will learn:

– A 101 approach to cycle validation and ancillary activities

– An expanded view of BIO/Bioburden and Cycle Calculation validation approaches

– A definition of annual review activities

– The first steps to cycle optimization


Day 2: If a cycle has been already validated and need to optimize

A.) Annual Requalification

B.) Annual review activities

C.) First steps to cycle optimization

D.) Regulatory considerations


Webinars in this series include:

Validating, Optimizing and Monitoring EO Sterilization Processes, Part 1


Presenters: Sterigenics

Complete the following information to access the webinar