March “In All Other News”: EC Rep Symbol Revised, Article 10a Flowchart, EHDS Regulation, and more
2 April 2025
UK MHRA vs EU MDR/IVDR Post-Market Surveillance (PMS): Overview of Gaps/Differences
8 April 2025Background
EUDAMED, the European Database on Medical Devices, is expected to become mandatory starting January 2026 (followed by a transition period): HERE
To help industry prepare, the EU Commission stated they would organize training sessions, including face-to-face events: HERE
Workshop Details
Objectives
The purpose is to help the stakeholders understand 1) what the mandatory use of EUDAMED will mean, and 2) raise awareness on the timelines for its use. The full overview is available: HERE
“By attending, participants will gain a clear understanding of how EUDAMED works, what information to provide, and when to integrate it into their regulatory processes.”
Location
It is being provided in hybrid format, allowing for both physical and remote participation. The physical location is at the Steigenberger Graf Zeppelin hotel, in Stuttgart, Germany.
Online attendees will receive the connection details by email one day before the event.
Event Date & Time
The workshop is scheduled for Wednesday 21 May 2025.
- Registration desk (to collect badge) opens at 9:00am Central European Time (CET)
- Event starts at 9:30am CET
Due to the start time, the workshop is optimal for participants in Europe and Asia-Pacific.
Language
The event will be conducted in English.
Fee
There is no fee to attend the workshop.
That said, if participants need to cancel for any reason, they are asked to email [email protected] as soon as possible, to allow other participants to join the event.
Deadline to Register
- Registration opens today (Monday 7 April 2025).
- To join in person, registration ends on Monday 5 May 2025.
- To join online, registration ends on Monday 12 May 2025.
How to Register
The registration link is: HERE
