FREE GUIDE
An Executive’s Guide to Transitioning from
Gamma to E-Beam
What to expect and how to lead a confident transition.
Performance and Compatibility Insights
Compare Gamma and E-Beam across effectiveness, limitations, and product fit. Learn how to assess whether your product is a good candidate for E-Beam sterilization.
Step-by-Step Transition Guidance
Understand the regulatory, technical, and validation steps required for a successful switch. Includes real-world cost and timeline estimates.
Scalable, Resilient Alternatives
Discover why leading teams are shifting to E-Beam in response to cobalt-60 shortages, regulatory support, and long-term sustainability goals.
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Why Executives Are Moving from Gamma to E-Beam
Safe
E-Beam avoids using radioactive cobalt-60, produces no radioactive waste, and relies on electricity, making it a safer and more sustainable alternative.
Compliant
ISO 11137 covers both E-Beam and Gamma sterilization, and both E-Beam and Gamma are regarded by the FDA as Established Category A modalities, helping simplify the regulatory path for switching modalities.
Precise
NextBeam's E-Beam sterilization process can be used to effectively eliminate all microorganisms / pathogens, helping to ensure the highest level of safety for your medical devices.