IVDR (EU) 2017/746: Critical milestone

IVDR (EU) 2017/746: Critical milestone

The implementation of the IVDR (EU) 2017/746 is marked by a series of key milestones that directly affect market access for in vitro diagnostic medical devices.

Date

22 January, 2026

Time

10:00-11:00 CET

Registration Deadline

19 January, 2026

Typology

Live Streaming

Language

English

Pricing

Free

Subscribe to the Webinar

This free webinar provides an in-depth analysis of the main IVDR milestones, including transitional provisions, device reclassification, conformity assessment procedures, the involvement of Notified Bodies, and the implications for technical documentation and quality management systems. Particular attention will be given to regulatory responsibilities, decision-making criteria, and risk-based prioritization for both legacy and new devices.

Participants will gain clarity on how these milestones impact legacy devices, new product development, and ongoing compliance strategies. The session will also explore the consequences of missed deadlines and highlight the importance of proactive planning to ensure business continuity under the IVDR framework.

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