Euro RAPS Convergence 2026

Visit our team at booth n°19, where we will be available to discuss your certification projects and answer your questions regarding the latest regulatory developments for medical devices and in vitro diagnostic medical devices.

This year, several GMED experts will contribute to the conference program:

• 5 May: Gaëlle Bisch, Certification Project Manager, Product Reviewer and Lead Auditor (DMDIV), will speak at the pre‑conference workshop on the technical documentation assessment of MDSW‑a.
• 6 May: Guillaume Berger, Deputy Manager and Certification Project Leader (DMDIV), will present during the session “Transitional timelines unpacked: EU 2024/1860 and its impact on legacy IVDs”.
• 7 May: Tom Patten, IVDR/IVD International Manager, will join:
  • as facilitator: “Solutions Circle: What the proposed IVDR changes mean for IVD manufacturers?”
  • as speaker: “Change notification process of IVD devices under the IVDR: Are you ready?!”
• 8 May: Tom Patten will return as:
  • facilitator for “Solutions Circle: What the proposed IVDR changes mean for IVD manufacturers?”
  • speaker for “AI‑powered conformity assessment: Transforming notified body operations”

We look forward to meeting you in Lisbon for four days of conferences, workshops, and exchanges with the European regulatory community.

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