Medical Device Directory

Overview of an Ethylene Oxide Sterilization Validation

A free white paper by STERIS Corporation

Prior to beginning routine ethylene oxide sterilization, a product with a sterile claim needs to complete a validation process to ensure the Sterility Assurance Level claimed is met. This TechTip will provide a step-by-step overview of an ethylene oxide validation process that complies with the guidelines established in 11135 using a Half Cycle Overkill Approach.

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