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Steri-Tek is an ISO 11137 and ISO 13485 certified, FDA registered, DEA registered as well as State of California Medical Device and Drug Manufacturing licensed facility serving the medtech, biotech, pharmaceutical and other industries.
The facility boasts two state-of-the-art 10 MeV, 20 KW linear accelerators, using simultaneous beam processing that allows for high volume production, providing uniform dose to the product without having to rotate the customer’s boxes. This DualBeam™ configuration significantly increases efficiencies, expands product options, and serves as an effective back-up for the accelerators. The facility will provide the most 10 MeV sterilization capacity, the most comprehensive product options, and the highest uptime availability than any other facility in North America.
Steri-Tek offers a seamless dose map validation of customer’s product from any other contract irradiator. Our staff of validation engineers will provide expert consultation for setting up any products to be dose mapped. We also offer turnkey sterilization validations for any new products to be introduced into the market at some of the most competitive rates.
Call us to learn more about how Steri-Tek can help you with your medical devices, pharmaceuticals, material modification, and food safety.