Webinar: Global UDI 2026 – EUDAMED, swissdamed & TGA Australia

Webinar: Global UDI 2026 – EUDAMED, swissdamed & TGA Australia

Webinar: Global UDI 2026 -EUDAMED, swissdamed & TGA Australia

Deadlines, Transition Periods and Practical Upload Solutions for Small and Large Companies

UDI requirements are becoming mandatory in several important markets in 2026. For medical device manufacturers, importers, distributors and authorised representatives, now is the right time to prepare for upcoming deadlines, transition periods and practical implementation requirements.

In our free webinar, we provide a compact and practical overview of the UDI requirements for EUDAMED, swissdamed and TGA Australia / AusUDID. We explain which deadlines are relevant, which transition periods apply and how companies can efficiently prepare, validate and submit their UDI data to the respective authorities.

A special focus will be placed on practical implementation: How can UDI data be submitted to swissdamed? What options are available for manual entry, XML upload or M2M interfaces? What typical data issues and validation errors may occur? And how can companies establish one global UDI data strategy instead of managing separate projects for each authority?

The webinar is designed for companies that want to structure their UDI processes in time, regardless of whether they manage a small product portfolio or large volumes of UDI data.

Webinar Topics

• Why UDI deadlines in 2026 matter now
• EUDAMED UDI: mandatory use, deadlines and transition period
• swissdamed UDI: Swiss deadlines, transition period and practical impact
• How to submit UDI data to swissdamed
• TGA Australia / AusUDID: deadlines and transition period
• Key differences between the EU, Switzerland and Australia
• One global UDI data strategy instead of separate authority projects
• Excel upload, data validation and authority-specific data transformation
• Easy UDI upload solution for small and large companies
• Live Q&A / FAQ

Date: 23 June 2026
German session: 10:00
English session: 14:00
Duration: approx. 1.5 hours
Participation: free of charge

This webinar is especially relevant for Regulatory Affairs, Quality Management, IT, Master Data Management and companies that need to prepare and submit UDI data efficiently for multiple markets.

To registrate please fill in below form:

Only business addresses, private addresses such as gmail.com, yahoo.com are not accepted.

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.