IVDR Implementation in 2026: What UK Diagnostic Manufacturers Must Do Now
The EU In Vitro Diagnostic Regulation (IVDR) is now fully in force, and UK manufacturers exporting into Europe face a dual compliance landscape — UKCA marking domestically and CE-IVD for European markets. Here is what your regulatory team needs to action before year-end 2026. <br/><br/> We break down the technical file requirements, the notified body bottleneck, and the practical steps to maintaining market access on both sides of the Channel — with expert input from speakers confirmed for FutureDX 2026.
