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48225 Lakeview Boulevard , Fremont, CA, 94538, US
Providing insight on the numerous considerations in switching sterilization methods, Rose LaRue-Slater of SteriTek explains what factors are most important.
By: Sean Fenske
Device manufacturers gain additional value from packaging and sterilization considerations when conducted early in the product development process.
By: Mark Crawford
With increasing concerns involving the use of ethylene oxide for terminal sterilization of medical devices, Larry Nichols of SteriTek speaks to other options.
Announced at IME West 2024, the new organization is designed to provide manufacturers with end-to-end solutions for launching new products.
By: Michael Barbella
With the spotlight on terminal sterilization, Jeff Sauter of SteriTek offers insights on what’s driving the interest in alternative techniques and technologies.
Join the company for an open house on September 28th.
By: Charlie Sternberg
With concerns growing over what actions the EPA and FDA may take with regard to EtO sterilization, SteriTek’s Larry Nichols explains the situation.
With uncertainty around EtO sterilization still swirling, Steri-Tek’s Jeff Sauter highlights the approach firms can take when considering alternatives.
Diagnostics manufacturers and supply chain partners have adapted to accommodate the enormous demand for COVID-19 tests amid disrupted operations.
By: Sam Brusco
How are service providers and component suppliers adjusting to life during a pandemic to ensure they maintain quality?
Jeff Sauter states how Steri-Tek addresses the numerous challenges medical device manufacturers face in ensuring sterility of their products.
Company’s event will take place March 15 and is open to all.
By: Steri-Tek
A device’s packaging needs to maintain the sterile barrier, but also needs to be compatible with the sterilization method.
High-volume e-beam/x-ray contract sterilizer and R&D innovation center provides on-demand services for medtech.
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