RQM+ is a global MedTech service provider focused on accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for Med Device and IVD companies, from concept to commercialization to post-market.

Our portfolio of services enables the delivery of end-to-end solutions across the complete med device product lifecycle, with our: 
• Regulatory and Quality Consulting
• Lab Services (Jordi Labs)
• Clinical Trials
• Reimbursement
• Technology Solutions


RQM+

The recently finalized EPA rule on ethylene oxide (EtO) emissions requires significant changes for sterilization facilities, potentially impacting manufacturers of sterile medical devices.

Join 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:

*   **Impact Assessment**: A detailed analysis of the new EPA rule, including how it affects EtO sterilization facilities and manufacturers of sterile medical devices.
*   **Compliance Strategies**: Guidance on softening EtO cycles to support the effort of reducing EtO emissions and ensuring compliance within the 2-3 year timeline.
*   **Alternative Sterilization Methods**: An overview of viable alternatives such as Vaporized Hydrogen Peroxide (VHP), radiation, and more. We will discuss their pros and cons, regulatory requirements, and validation processes.
*   **Quality and Regulatory Support**: Insights into design quality engineering, manufacturing quality engineering, regulatory change impact assessments, and more.
*   **Industry Perspectives**: An examination of feedback from industry stakeholders and how companies are adapting to these changes.

**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.

**Complete the form on this page to stay ahead of these critical regulatory changes and ensure the continued success of your sterilization processes.**

We hope to see you on Thursday, 18 July!

**Panelists:**

*   Jessica Dreyer – Senior Consultant, RQM+
*   Gregory Murdock – Senior Manager, RQM+
*   Jon Gimbel, Ph.D. – Vice President of Technical, RQM+ (moderator)
