Live! #80 panel | Recorded 18 July 2024
The recently finalized EPA rule on ethylene oxide (EtO) emissions requires significant changes for sterilization facilities, potentially impacting manufacturers of sterile medical devices.
Listen to our expert panel to understand the implications of these new regulations and discover actionable strategies to explore potential mitigation activities.
In this comprehensive discussion, our experts will cover:
Who Should Attend: This panel discussion is ideal for regulatory affairs professionals, quality engineers, manufacturing leaders, and medical device manufacturers who rely on EtO sterilization or are considering alternative methods.
By attending this event, you will gain a clear understanding of the new EtO regulations, learn practical steps to mitigate for compliance-led changes at your sterilization facilities, and explore alternative sterilization methods to ensure your products remain safe and market-ready.
Please complete the form to watch the recording and download the slides.
Panelists:
Certificate of Participation available upon request for live attendees.
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