TechTips

This TechTip discusses the overall requirements, use of surrogate materials and application of reference dosimetry during routine gamma irradiation

This TechTip reviews the variables that should be considered to assure the EO sterilization process is effective each and every time.

This article will review the top seven items to consider from a reprocessing point of view in the design and commercialization of reusable instrumentation.

Test method validation for adverse and/or inhibitory substances is important to ensure that the measurement of contamination on a device is not impacted by substances present in the test. Adverse substances and/or inhibitory substances (e.g. antimicrob

Learn about the factors to take into consideration when choosing an ethylene oxide contract sterilization facility.

This TechTip provides a summary of minimizing over-processing by understanding how to establish an appropriate internal process challenge device. Let our team review your process and identify other ways to help reduce EO sterilant used through our Sustainable EO® sterilization services

This TechTip focuses on why some starches require irradiation, effects of radiation on starches, and suggestions for evaluating minimum and maximum doses

This TechTip provides information on the selection of an appropriate Sterility Assurance Level (SAL) for medical devices

A study was carried out to compare the impact, if any, of EO concentration on product EO residual levels determined in accordance with ISO10993-7.

As part of our commitment to providing innovative and sustainable solutions, STERIS AST has developed the Sustainable EO® sterilization services program.