EUDAMED November Deadline: What Global Medical Device Manufacturers Need to Do Now
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 global manufacturers need to do to meet the upcoming EUDAMED requirements, where to focus your efforts now, and how to accelerate 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 that place products on the EU market.
Don’t wait until November to discover a data problem
Join us to understand what the EUDAMED deadline means for global manufacturers, assess where your organization stands today, and determine what to prioritize now to make the remaining time count.