Testing & Validation
ETO sterilization involves several stages, including pre-conditioning, sterilization, and aeration. During pre-conditioning, the materials to be sterilized are exposed to a controlled level of humidity to prepare them for the sterilization process.
The materials are then placed in a sterilization chamber, where they are exposed to a controlled amount of ethylene oxide gas for a specific amount of time. After sterilization, the materials are aerated to remove any remaining gas and ensure that they are safe for use.
Our laboratory testing and product and packaging testing services provide Customers with validation support and microbial testing, ensuring medical devices processed with EO perform as expected for the life of the product, and packaging maintains the sterility of the device until its point of use.
Our current industry client includes disposable medical devices products (such as surgical gloves, syringes, etc.).
