Date & Time
Starts
Jun 16, 2026 10:00am CST
Ends
11:00am CST
Location
Online
Language
English
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. Join Emergo by UL on June 16, 2026, from 10-11 a.m. (CST) for an informative webinar focused on unique device identification (UDI) regulatory change. This is a follow-up to our May 2026 presentation on the European Database on Medical Devices (EUDAMED).
Focus on global UDI changes
Many organizations are now gearing up for what comes next. This webinar will take a look at how UDI will impact other global markets beyond the U.S. and 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 will provide 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.
Key takeaways
- 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
Who should attend?
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
- Operations and data governance stakeholders supporting regulatory reporting
Looking for up-to-date, practical guidance?
Register today to save your seat for Tuesday, June 16, 2026, from 10-11 a.m. (CST).
Upcoming UDI webinar
Beyond the Guidance: Lessons from Applying Two Years of NMPA HFE Guidance
Our May 28 webinar is the first in a two-part series on unique device identification (UDI) compliance beyond the U.S. and the EU.
Upcoming UDI webinar
EUDAMED Explained and What’s Coming
Join us on May 28, 2026 from 10-11 a.m. CT for an informative and practical webinar about the European Database on Medical Devices (EUDAMED), a cornerstone of the EU Medical Devices Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR).
About the presenter
Linda Chatwin has over 35 years of experience with medical products. Through years of watching regulations evolve and change, she knows how to navigate the global regulatory maze and bring products to market. Ms. Chatwin has obtained approvals for a wide range of products and remains involved in changing requirements for medical devices worldwide. She has navigated many U.S. Food and Drug Administration (FDA) inspections and other regulatory authority audits and negotiated favorable outcomes with the FDA. Currently, she assists clients with regulatory issues and challenges, including implementation of UDI processes, mock audits, in-depth training on regulatory requirements, and consulting on quality system development and improvement and the Medical Device Single Audit Program (MDSAP) audit model. She has also conducted numerous trainings and gap assessments for the new Medical Device Regulation (MDR), as well as software as a medical device (SaMD) requirements.
Join us!
Learn about evolving UDI compliance in this webinar featuring insights on known requirements, emerging reporting databases and proactive monitoring strategies.