November 5 - 7, 2024
The Royal Sonesta Minneapolis DowntownMinneapolis, MinnesotaNovember 5 - 7, 2024
The Royal Sonesta Minneapolis Downtown,
Minneapolis, Minnesota
The Royal Sonesta Minneapolis Downtown,
Minneapolis, Minnesota
Consolidate your IVDR Knowledge and Achieve Compliance with Confidence
Dive Into The Significant Changes Under Article 110(3), Companion Diagnostics, and EU IVDR Expert Panels
Connect with thought leaders including TÜV SÜD, Abbott, Agilent, and Thermo Fisher Scientific
Accelerate Your Path To EU IVDR Compliance With Expert Guidance
Multi-Stakeholder Perspectives
- Optimizing transitions from IVDD to IVDR
- Reflecting on 6 months post-IVDR date of application from TÜV SÜD
- Navigating significant changes under Article 110(3)
Accelerating Your IVDR Compliance
- Outlining the future of companion diagnostics on a global scale with Covington & Burling
- Step by step guidance on successful IVDR submissions
- Lessons from PECP and navigating expert panels by Thermo Fisher Scientific
Initial Feedback from Key Players
- Case study example on completing technical documentation with Agilent
- First hand experiences class D conformity assessment from TÜV SÜD
- Conducting Clinical Trials in line with IVDR
EU IVDR Compliance: Time Critical Insights From An Expert Speaker Line-Up
Gain leading implementation and compliance advice from FDA, Notified Bodies & IVD Manufacturers
