Scilife Training | Preparing for EUDAMED: what medical device companies need to do now

Scilife Training | Preparing for EUDAMED: What Medical Device Companies Need to Do Now

With the phased rollout of EUDAMED approaching, many MedTech companies still lack clarity on what it is, who must register, and how to prepare.

To address this, a dedicated training session will provide a clear, structured overview of EUDAMED and guide quality and regulatory teams from uncertainty to practical readiness. The session will focus on immediate steps companies need to take, based on real experience supporting organizations through EUDAMED registration.

Training | Preparing for EUDAMED: What Medical Device Companies Need to Do Now

February 24, 2026 | 11:00H (CET)

The session will cover:

• Understanding what EUDAMED is and how it fits into the EU MDR framework

• Navigating the EUDAMED rollout timeline and the first modules to go live

• Identifying actor roles and responsibilities within EUDAMED

• Preparing organizations for actor registration and future module use

The webinar will feature Karandeep Badwal, Founder and Principal Consultant at QRA Medical, and Angel Buendía, Knowledge Manager at Scilife.

The training offers a practical overview of EUDAMED and the actions medical device companies need to take now.

Registration Link: Register here for free