This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Regulation, Clinical and Software for Medical Devices


  • 00
  • 00
  • 00
  • 00
November 5 - 7, 2024
The Royal Sonesta Minneapolis DowntownMinneapolis, Minnesota

Navigate the Complexities of ISO 10993 Updates to Benchmark Best Practices & Shape Future Regulations

Spotlight on ISO 10993-1, Part 17 & 18 Insights, Biological Evaluation Plans, Biostability, ISO 18562, Shelf Life, and more!

Immerse Yourself in the Discussion with Keynote Sessions, Case Studies, and Panels Compiled from TC 194, Notified Bodies and Medical Device Pioneers

Implement Biological Evaluation Plans For Your Medical Devices With Confidence

Navigate Top Tier ISO 10993 Updates as They Happen

  • Hear from TÜV SÜD on the latest updates to 10993-1
  • Implement best practices to adhering to 10993-17 with help from Abbott, Boston Scientific and Medtronic
  • Delve into 10993-18 revisions alongside SGS, Stryker, and Abbott

Gain First-Hand Experiences Through Interactive Discussions

  • Understand the latest on global in vitro acceptance through our multi-stakeholder panel
  • Have any remaining burning questions answered with our ‘Ask the Experts’ panel
  • Explore the future of Biocompatibility regulation

Understand the Building Blocks to Curating a Biocompatibility Strategy

  • Conquer biological evaluation reports with help from ConvaTec and Boston Scientific
  • Hear from Medtronic on how to justify biocompatibility data under EU MDR
  • Address necessities of good laboratory practice through Cardinal Health’s lessons learned