TechTips

This TechTip provides 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.

Sterilizing medical devices with ethylene oxide (EO) is a common practice primarily due to its extensive material compatibility. This TechTip discusses the residues that may be found after EO processing and residual reduction methods.

Learn more about our global offering, which includes electron beam, gamma, X-ray, and ethylene oxide technologies

This TechTip provides an overview of the parametric release process, including microbiology requirements, equipment requirements, process analysis and load configuration.

Overview and detailed steps of Process Method C, the most commonly used method for an ethylene oxide performance qualification.

Do improvements to your medical device impact a currently-validated EO process? View our TechTip to learn about product adoption for ethylene oxide sterilization

Product and Packaging Testing Frequently Asked Questions (FAQ) Q1: Per ISO and ASTM standards, is there a recommendation on when a transportation simulation should be performed on aged samples (i.e. after accelerated aging/real-time aging or shelf-life

This TechTip focuses on what Customers need to know before initiating changes to product packaging in order to ensure that the efficiency and effectiveness of the gamma process is maintained

This overview covers steps and other considerations for the qualification of new medical devices that will be processed with gamma radiation.

View a sample list of products commonly treated with gamma irradiation, examples where gamma is the method of choice and factors preventing the use of other sterilization technologies