THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.
Date & Time
Starts
May 28, 2026 10:00am CST
Ends
11:00am CST
Location
Online
Language
English
Upcoming webinar on EUDAMED compliance
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).
Designed to increase transparency, traceability and regulatory oversight, EUDAMED brings together actor registration, unique device identifier (UDI) data, certificates, clinical investigations, vigilance and market surveillance into a single, interconnected system.
While not all EUDAMED modules are yet mandatory, regulators and notified bodies increasingly expect companies to be EUDAMED ready. With several modules already live and transition periods moving quickly, manufacturers have limited time to prepare.
What you’ll learn
- What EUDAMED is, how the database is structured and each module works
- EUDAMED obligations that apply now
- Implementation timelines
- EUDAMED readiness gaps seen across the industry
Who should attend?
This webinar is ideal for:
- Regulatory affairs professionals
- Quality and compliance leaders
- Market access teams supporting EU commercialization
- IT and data owners supporting MDR/IVDR readiness
Looking for up to date, practical guidance?
If the EU is part of your commercial or regulatory strategy, this session is essential. Save your space today for this webinar on May 28, 2026 from 10-11 a.m. (CT).
Upcoming UDI webinars
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.
The next chapter, scheduled for June 16, 2026, will dive into how different markets are implementing UDI and how reporting databases and rules vary.
About the presenter
Tom Ingless, senior quality and regulatory affairs consultant, Emergo by UL
Tom Ingless is a UK-based consultant with more than 10 years of experience supporting medical device manufacturers in achieving and maintaining compliance with European regulations. He is skilled in the preparation, development, and remediation of technical documentation, including Clinical Evaluation Reports (CERs).
Tom works closely with customers to deliver pragmatic, audit‑ready regulatory solutions, including MDR gap assessments, high‑quality technical file and CER authoring, EUDAMED readiness, and end‑to‑end support for CE and UKCA marking.
As part of Emergo’s Clinical Evaluation and Authorised Representative programmes, Tom focuses on helping customers demonstrate current European regulatory and clinical evidence requirements as they work to bring medical devices to market.
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Learn more about EUDAMED structure, key dates and steps to take to support readiness.
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