Training Schedule and Live Stream Links
These training sessions require no registration and are completely free of charge, open to manufacturers, Authorized Representatives, Notified Bodies, regulatory authorities, and all professionals following EUDAMED developments. Each session lasts 9 hours and includes demonstrations and Q&A. Please note the time difference between Central European Summer Time (CEST) and Beijing Time and plan your viewing accordingly:
- Actor Module
- EU time:
April 28, 9:00–18:00 CEST - Beijing time:
April 28, 15:00 – April 29, 0:00 - Live stream link:
https://webcast.ec.europa.eu/eudamed-actor-module-workshop-2026-04-28
UDI/Devices Module
- EU time:
May 5, 9:00–18:00 CEST - Beijing time:
May 5, 15:00 – May 6, 0:00 - Live stream link:
https://webcast.ec.europa.eu/eudamed-devices-module-workshop-2026-05-05
Notified Bodies & Certificates Module
- EU time:
May 7, 9:00–18:00 CEST - Beijing time:
May 7, 15:00 – May 8, 0:00 - Live stream link:
https://webcast.ec.europa.eu/eudamed-certificates-module-workshop-2026-05-07
The official EU announcement confirmed the training arrangements above. Click the relevant link to access the European Commission’s streaming platform and watch the live session free of charge.
Why should you pay close attention to EUDAMED?
EUDAMED (the European Database on Medical Devices) is the central hub of the EU regulatory framework, used to collect and make public registration information for medical devices and in vitro diagnostic products, Notified Body certificates, market surveillance data, and more. From May 28, 2026, use of the following modules will shift from voluntary to mandatory:
- Actor Registration
: Manufacturers, authorized representatives, system or procedure pack producers, and others must register in this module and obtain an SRN. - UDI/Devices Registration
: New MDR/IVDR products must have their UDI and related device information entered before being placed on the market. - Notified Bodies & Certificates
: Notified Bodies must upload certificate information, and manufacturers must confirm the correspondence between certificates and products. - Market Surveillance
: Competent authorities will publish market surveillance data through this module.
If you have not yet started your EUDAMED preparations, this training is a valuable opportunity to gain an in-depth understanding of the workflows and requirements of each module and prepare for the upcoming mandatory deadline.
Participation recommendations
Test your network connection in advance to ensure smooth access to the EU streaming platform. Prepare your questions during the training; the instructors will address common questions during the Q&A session. After the training, promptly consolidate the key takeaways and plan your company’s internal EUDAMED compliance roadmap.
Please feel free to share this article with your network, WeChat groups, and industry communities so that more colleagues can learn about this important notice. Follow this account for continued updates on EU medical device regulations and the latest developments in global compliance.
End of article. If you would like further consultation on EUDAMED preparation or to discuss training takeaways, please leave us a message.