WEBINAR - Will the 2025 Proposal Flip Your IVDR Priorities?

The IVDR transition continues to evolve, and 2026 represents a pivotal moment for manufacturers to reassess their regulatory roadmap. Regulation (EU) 2024/1860 extends the transition period for eligible legacy devices, offering companies additional time to achieve compliance. However, while the timeline has shifted, the core IVDR requirements remain unchanged. At the same time, the targeted 2025 revision proposal introduces new strategic considerations that may influence long-term portfolio and compliance planning.

To help regulatory and quality leaders navigate this shifting landscape, ProductLife Group is hosting a dedicated webinar exploring how manufacturers can leverage the extended transition period without losing momentum. The session will examine how to secure QMS readiness, Notified Body engagement and performance compliance, while reassessing portfolio priorities based on risk and value. It will also address how organisations can position themselves for potential regulatory adjustments without overreacting to uncertainty.

• Leveraging the extended IVDR transition period while maintaining compliance progres
• Ensuring QMS, Notified Body and performance readiness
• Reassessing portfolio strategy based on risk and business value
• Preparing for potential regulatory shifts linked to the 2025 targeted revision proposal

Samuel Buet, Consultant Manager MD & IVD
Jordan Delisle, Consultant Manager MD & IVD

🗓️ 26 February 2026 | 🕒 10:00 AM CET

📍 Format: Free online webinar held in English