EUDAMED November Deadline: What Latecomers Can Still Do Before It’s Too Late
The November EUDAMED deadline is approaching fast. Is your UDI registration ready?
If your device data is not yet fully registered or you’re unsure whether your current data will meet EUDAMED requirements, now is the time to focus on what matters most.
Speakers
Join our experts for a practical webinar designed for medical device and IVD manufacturers still working toward the EUDAMED deadline:
- Lionel Tussau, Chair of the MedTech Europe EUDAMED IT Group, Member of the GS1 Global Healthcare Leadership Team, and Lead Healthcare for Medical Devices (BYRD Health) at osapiens
- Henning, General Manager for Medical Devices at osapiens
They’ll break down what needs to be done, where to focus your efforts, and how to accelerate your EUDAMED registration without creating data-quality or compliance issues that will need to be fixed later.
Webinar Agenda
- November deadline: what exactly needs to be done and by when?
- Are you behind? How to assess your current EUDAMED readiness
- What data need particular attention
- Latecomer action plan: what to prioritize between September and November
- 7 steps to register devices efficiently
- Common data-quality and MDR/IVDR conversion pitfalls
- What happens after November: EUDAMED as an ongoing compliance process
- Q&A
Who should attend?
This webinar is for Regulatory Affairs, Quality, Master Data, and EUDAMED/UDI project teams at medical device and IVD manufacturers, especially organizations that are still preparing device data, completing registrations, or assessing whether they are ready for the November deadline.
Don’t wait until November to discover a data problem
Join us to understand where you stand, what to prioritize now, and how to make the remaining time count.