THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.
Focus on global UDI changes
Many organizations are now gearing up for what comes next. This webinar examines how UDI will impact other global markets beyond the U.S. and the EU. While there is growing alignment around UDI barcoding standards, the reality is far more complex and markets around the world are developing their own reporting databases, compliance timelines and data expectations. Some may share similarities with existing frameworks, while others introduce new requirements that companies must interpret, track and operationalize. For organizations operating across multiple regions, this creates an increasingly dynamic compliance environment.
What you’ll learn in this webinar
This webinar provides a practical overview of how different markets are approaching UDI, where requirements are already defined and where change is still underway. Emergo by UL experts will also discuss why staying vigilant is critical as regulations continue to mature and enforcement expectations increase.
How UDI requirements are evolving beyond the U.S. and EU
Which global markets have defined compliance timelines and which are still developing them
An overview of reporting databases being used or planned in key regions
Where similarities and differences exist across global UDI frameworks
Watch now: Global considerations beyond US and EU EUDAMED
UDI is becoming a foundational element of medical device compliance. In the United States, UDI has been fully implemented and is operating at scale, and the European Union is also moving forward with EUDAMED. This follow-up to our May 2026 presentation on the European Database on Medical Devices (EUDAMED) is focused on unique device identification (UDI) regulatory change.
Webinar date
June 16, 2026
Speaker
Linda Chatwin, Esq. RAC, Lead Regulatory and Quality Consultant
Attend an upcoming webinar
Ready to elevate your industry IQ with insights and news from experts? Register for one of our upcoming events.
To watch the webinar, please fill out the form below:
If your organization markets medical devices in multiple countries or plans to expand globally, this session will help you better understand the shifting UDI landscape and how to prepare for what lies ahead. This webinar is designed for professionals responsible for global medical device compliance, including regulatory affairs leaders and managers, quality and compliance professionals, product and labeling teams involved in UDI execution, and operations and data governance stakeholders supporting regulatory reporting.
Please wait…