Preparing for EUDAMED: what medical device companies need to do now
Many MedTech companies are still unclear on what EUDAMED is, who needs to register, and what data and processes must be in place ahead of the rollout. Meanwhile, delays and registration issues are already starting to surface.
That’s why we’re hosting a free training to walk through EUDAMED in a clear, practical way, based on real registration experience, not theory.
With the phased rollout of EUDAMED approaching, many MedTech companies still lack clarity on what it is, who must register, and how to prepare.
That’s why we’re hosting this training: to provide a clear, structured overview of EUDAMED and help quality and regulatory teams move from uncertainty to practical readiness. The session will focus on what you need to do now, based on real experience supporting companies through EUDAMED registration.
We’ll show you how to:
- Understand what EUDAMED is and how it fits into the EU MDR framework
- Navigate the EUDAMED rollout timeline and what is going live first
- Identify actor roles and responsibilities within EUDAMED
- Prepare your organization for actor registration and future module use
You’ll hear from Karandeep Badwal, Founder and Principal Consultant at QRA Medical and Angel Buendía, Scilife’s Knowledge Manager.
📅 February 24th, 2025 | 11:00H (CET)
A practical overview of EUDAMED and what medical device companies need to do now.