The IVD landscape continues to evolve. Are you ready for what's next?
IVDR implementation continues to challenge manufacturers, laboratories and notified bodies alike. Expectations are evolving, legacy device transitions are underway, and performance evaluation requirements are becoming increasingly important, particularly for software IVDs.
The IVD track at the Medtech Compliance Forum by Aurevia & RAPS brings together experts to discuss:
In-house tests under the IVDR and competent authority expectations for clinical laboratories
What notified bodies expect from IVDR performance evaluation of software IVDs
The future of European diagnostics and the impact of the IVDR revision
Strategies for navigating the transition of legacy devices
How to maintain your CE certificate through follow-up audits and real-world challenges
Join speakers from Fimea, SGS, Healthtech Finland, DNV and Aidian for practical insights designed to help IVD professionals navigate today's regulatory requirements and prepare for tomorrow's changes.
As part of Labquality Days, attendees also gain access to one of Northern Europe's largest gatherings in laboratory medicine and health technology.
Explore the scientific programme
📍 Helsinki, Finland (Part of Labquality Days)
📅 11-12 February 2027