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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