How is EtO residuals testing performed?
Learn what ethylene oxide residuals are and how EtO residuals testing for medical devices and other products is performed.
Learn what ethylene oxide residuals are and how EtO residuals testing for medical devices and other products is performed.
Learn about medical device sterilization options and which one is the best to sterilize your medical devices following regulatory requirements.
Learn what USP 88 cytotoxicity tests are available and which ones you will need to meet the regulatory requirements for your medical devices.
Learn what USP 87 cytotoxicity tests are available and which ones you will need to meet the regulatory requirements for medical products.
Learn how to perform endotoxin and pyrogen tests for your medical device, and identify which tests will be needed for your device.
Learn how the FDA defines medical devices, 510(k) submission types, and the approximate cost for developing new medical devices.
Learn about biocompatibility tests for medical device and implant regulatory requirements, USP guidance, and medical devices categorizations.
Learn about what product samples will need to be sent and when for Ethylene Oxide (EtO) residuals testing of sterilized medical devices.
Learn about in-vitro vs. in-vivo medical device cytotoxicity assessments, and requirements of USP 87 and USP 88.
Learn about the methods used to measure ethylene oxide (EtO) residuals via exhaustive extraction for medical devices and products.