For medical devices and other materials sterilized by ethylene oxide, a key safety requirement is to demonstrate that product has safe levels of residual ethylene oxide and related substances after aeration. iuvo has a long history of assaying for residual ethylene oxide, ethylene chlorohydrin, and ethylene glycol sterilization residuals per ANSI/AAMI/ISO 10993-7:2008/(R)2012.
Work closely with our sterilization validation consulting team
Our chemistry team works closely with our sterilization validation consulting team to provide you with broad expertise to answer any questions you may have and to provide you with fast, reliable testing.
To contact our specialists or learn more about our services, please reach out to us, and we’d be happy to help you with your application.
Contact Us Today
If you’re seeking comprehensive medical device services, look no further than iuvo Bioscience. Our experienced team is ready to assist you with testing, evaluation, and regulatory support to ensure successful commercialization of your medical device. Contact us today to discuss your project and learn how our expertise can help you get to market fast.