4th Edition Excellence in Sterilizing Medical Devices
May 3 to May 4, 2023
Chicago, Illinois, United States
With advances in changing modalities due to reduced capacity, the industry is challenged to shift their thinking not just to increase capacity but to reduce cycle times, make modality choices and modify sterility validations while keeping up with regulatory changes and maintaining device quality. This event brings together voices from sterilization stakeholders to define and build the future of this industry, for the benefit of the patients.
This conference will provide attendees with lessons learned and recent approaches on Chemical Characterization, Classifications for Hazardous Chemical Substances, In Vitro vs In Vivo Testing, Toxicological Risk Assessments, and Product Lifecycle Management. Additionally, attendees will walk away with actionable takeaways about how to navigate evolving regulatory guidance and standards related to ISO10993, the EU MDR, US FDA, and other global regulatory and standards organizations. Furthermore, the sessions will explore solutions to the challenges associated with testing and manufacturing such as material availability, alternative materials, supplier diversification, manufacturing transfers, and more.
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