Join our webinar to discover what it takes to gain control over your sterilization process!

Medical device manufacturers are increasingly re-evaluating outsourced sterilization models that rely on ethylene oxide, gamma, or x-ray processing. Long lead times, supply chain disruptions, environmental concerns, shipping costs, and limited process control are driving interest in bringing sterilization in-house. 

This webinar explores how electron beam (e-beam) sterilization can provide a viable alternative for manufacturers seeking greater operational control, faster turnaround, and a more environmentally responsible approach—without the use of harmful chemicals and the residuals they leave behind. We will discuss key considerations for transitioning from third-party sterilization services to an in-house model, including facility integration, dose requirements, throughput planning, and compliance within ISO-11137 irradiative sterilization standards. 

Drawing on real-world engineering experience, Wasik will outline how e-beam systems can be designed and scaled to fit existing production environments and tailored to the specific dose requirements of individual products. Attendees will leave with a clearer understanding of when in-house e-beam sterilization makes sense, what challenges to anticipate, and how it can supportsupply chain resilience, minimize operating expenses, and help achieve sustainability goals.