Expose your device to the EO sterilization process for non-human contact purposes. We can determine worst-case-scenario parameters for your R&D study. We can also match the parameters of larger sterilization chambers to save you time and money when you need samples fast.

Perfect for: engineering studies, packaging studies, biocompatibility studies, etc.

Turnaround Time: 24 - 48 hours

Routine processing of your medical devices using the validated parameters.

Turnaround time: 24 - 48 hours

Ethylene Oxide Sterilization Validation per ISO 11135:2014. We write the protocol, conduct the necessary cycles, test the biological indicators, and write the final report. We can also help you coordinate the biological and EO residual tests to complete the validation as fast as possible.

Turnaround time: 4 weeks

Need a batch of sterile devices for a clinical trial but not ready for a complete sterilization validation? Conduct a batch release to quickly release product.

Turnaround time: 3 weeks

Quickly and easily qualify your previously validated cycle in our sterilization chambers.

Turnaround time: 1.5 weeks

Qualify a change to your medical device, a change to the packaging, or an addition to your product family.

Turnaround time: 1.5 - 3 weeks - varies depending on the testing required.

MASS-EO's Columbus, OH facility is able to conduct all types of EO sterilization studies on-site, but if you have your own sterilizer and need expert help on conducting your qualification activities, we can help with that as well! Contact us to discuss your project today!