The Business Impact of EUDAMED on Market Access
The European Database on Medical Devices (EUDAMED) is often viewed by manufacturers purely as a compliance burden when…
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EUDAMED & swissdamed: Mandatory Registration for 2026
Preparing for EUDAMED & swissdamed As global regulatory systems continue evolving, medical device manufacturers must stay ahead of changing requirements…
EUDAMED Registration Mistakes and How to Avoid Them
The European Database on Medical Devices (EUDAMED) is a centralized electronic system established under…
The Business Impact of EUDAMED and Staying Compliant
The European Database on Medical Devices (EUDAMED) is often viewed by manufacturers purely as a compliance burden, serving…
EUDAMED and swissdamed Mandatory Registration Requirements
Mandatory registration in EUDAMED and swissdamed is finally here. By 28 May 2026, manufacturers marketing medical devices and IVDs in the EU must have completed their EUDAMED…
EU Confirms EUDAMED Functionality and 2026 Deadline
The European Commission has officially confirmed that several key electronic systems within the European Database on Medical Devices (EUDAMED) are…
EUDAMED: A Guide for Medical Device and IVD Manufacturers
The Medical Devices Regulation 2017/745 (MDR) and In Vitro Diagnostics Regulation 2017/746 (IVDR) introduced the requirement for a new…
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