August “In All Other News”: Proposed Cybersecurity Amendments, MDCG 2024-14 Revised, and more
5 September 2025
EU Commission Launches Call for Feedback: Targeted Revision of the MDR & IVDR (8 Sep–6 Oct 2025)
8 September 2025Background
EUDAMED, the European Database on Medical Devices, is expected to become mandatory starting Q1 2026 (followed by a transition period): HERE
To help industry prepare, the EU Commission has scheduled several training workshops. The first was conducted in May 2025, as a hybrid in-person and online session in Germany.
New EUDAMED Workshops
The Commission has opened up registration for the final two workshops of 2025: HERE
Purpose
The purpose of the workshops is to “help the stakeholders of the medical device sector to understand what the mandatory use of EUDAMED will mean and raise awareness on the timelines for its use”.
Logistics
Like the previous session, these will be:
- Conducted in a hybrid format, allowing both in-person and virtual attendance.
- Free of charge.
- Run from 9:30am – 5:45pm Central European Time.
- Conducted in English.
- The recording will be made available afterward, if participants are unable to join either of the live sessions.
Registration
The link to register is available: HERE
Note that you may only register for one of the two workshops. If you are not selected, due to workshop capacity, the recording will be published later on the Commission’s website.
