regularia 2026: Recap

regularia 2026: Recap

regularia 2026:
Recap – Exchange on MDR, Digitalization & UDI

On Tuesday, March 2nd, 2026, we were present at regularia 2026 – with our booth in the entrance area. The focus was on UDI/EUDAMED, data quality, and efficient digital regulatory workflows.

Once again, regularia 2026 showed how strongly regulatory requirements and digitalization are converging. The agenda highlighted topics such as MDR, material compliance, the digitalization of Regulatory Affairs & Quality Management, sustainability/Green Deal, international registrations, as well as cybersecurity/software/the AI Act.

As an exhibitor, we were on site at booth no. 12 (entrance area) and presented practical workflows for UDI data processes—from upload and validation through to transmission and proof of submission.

We also demonstrated how status and error monitoring as well as audit trails can be implemented cleanly within RA/QM processes, and how a unified data backbone supports international scaling (e.g., EUDAMED, FDA GUDID, Swissdamed, TGA).

Thank you to all visitors for the great conversations—we’re taking away many valuable insights and look forward to the next steps with you.

Ugur Müldür

Ugur Müldür leads Sales & Marketing activities at Europe IT Consulting GmbH in Basel, Switzerland. With an industrial engineering background, he bridges regulatory requirements, business needs, and IT implementation for UDI programs. He works with MedTech manufacturers to improve data quality, streamline submissions, and operationalize UDI solutions across global regulations.