Swissdamed & Switzerland: UDI – What to Watch, What to Prepare, and How to Avoid Rework
How can organisations prepare for Swissdamed without duplicating work on existing UDI and product data?
Join p36’s live webinar to learn what matters in the Swiss UDI landscape,
what is already known and which developments organisations should continue
to monitor.
Swissdamed is not simply an extension of EUDAMED. While existing UDI and
product data can provide a valuable starting point, Swiss-specific actors,
responsibilities, data requirements and submission processes need to be
addressed separately.
During the webinar, you will learn how to structure your preparation in a
risk-based way and avoid unnecessary rework. The session will cover what can
potentially be reused from EUDAMED, where Swissdamed-specific adjustments
are required and which next steps are relevant for your organisation.
Date and time
Tuesday, 13 October 2026, 2:00 p.m. CET
Unable to attend live? Register anyway to receive access to the recording,
presentation slides and a practical readiness checklist.
What you will learn
After the webinar, you will have a clearer understanding of:
- What is currently known about Swissdamed and Swiss UDI requirements
- Which regulatory developments and information organisations should continue to monitor
- Which existing EUDAMED content can serve as a starting point
- Where Swissdamed-specific adjustments are required across data, processes and responsibilities
- How responsibilities are divided between manufacturers, Swiss Authorised Representatives (CH-REPs) and other actors
- How to structure a risk-based preparation plan, including what to do now, next and later
- How to avoid unnecessary rework when preparing for Swissdamed
Who should attend?
This webinar is aimed at professionals and decision-makers in the medical
device, pharmaceutical, biotechnology and other regulated industries who are
responsible for UDI, product data, regulatory requirements or market access
in Switzerland.
- Regulatory affairs and market access professionals
- UDI and product data managers
- Quality and compliance managers
- Medical device and in-vitro diagnostic professionals
- Regulatory and master data experts
- Manufacturers and Swiss Authorised Representatives
- Project leads preparing for EUDAMED and Swissdamed
Your speakers
Milena Gözcü
Team Lead UDI Service & Delivery
p36 GmbH
Thomas Pauly
Practice Manager CSV & Compliance
DHC GmbH