1MED Heading to Lisbon for RAPS Euro Convergence 2026: Focus on Data Quality and MDR
We are thrilled to announce that 1MED will be participating in the RAPS Euro Convergence 2026, one of Europe’s premier events for regulatory professionals. The conference will take place in the beautiful city of Lisbon, Portugal, from May 5th to 8th.
As the MedTech landscape continues to evolve under the Medical Device Regulation (MDR), staying ahead of compliance and clinical requirements is more critical than ever. 1MED is proud to be at the forefront of these discussions.
Join Our Featured Presentation
We are honored to invite you to a high-level technical session that addresses one of the most pressing challenges in the industry today: the integrity of clinical data.
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Presentation: How to Ensure Data Quality and Reliability in Clinical Trials and PMCF under MDR
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When: Thursday, May 7, 2026, at 1:00 PM
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Speakers:
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Enrico Perfler – Founder, 1MED SA
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Christine Beulshausen – Global Expertise Manager Clinical Audit at TÜV SÜD, Project Manager MedTech GCP Service – TÜV SÜD
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Why This Session Matters
Maintaining MDR compliance requires a rigorous approach to clinical data and Post-Market Clinical Follow-up (PMCF).
In collaboration with TÜV SÜD, we will explore best practices and strategies to ensure that the data you collect is not only reliable but also robust enough to withstand the scrutiny of Notified Bodies.
Visit us at Booth 33
Throughout the four-day event, 1MED will have a dedicated booth in the exhibition hall. Our team of experts will be on hand to discuss your specific clinical and regulatory strategies, answer questions about MDR/IVDR, or simply catch up on the latest industry trends.
We look forward to seeing you in Lisbon!
