swissdamed webinar: requirements, deadlines, and how to prepare

Switzerland is introducing swissdamed, Swissmedic’s database for registering economic operators and medical devices (UDI). The Actors module is already live, and device (UDI) registration becomes mandatory from July 1, 2026. This session focuses on what the rules require, what applies to your role in the supply chain, and how to get ready without creating unnecessary rework alongside EUDAMED. 

This session be headed by Lionel Tussau, Lead Healthcare at osapiens.  

Lionel works with medical device manufacturers and healthcare organizations on turning regulatory requirements into repeatable processes, connecting regulatory, master data, and operational teams, so compliance is manageable at scale. He brings a clear, implementation-oriented view of what swissdamed will mean for day-to-day work, and how to avoid common pitfalls when deadlines approach. 

If you’re responsible for medical device compliance, UDI/master data, quality, or market access in Switzerland or Liechtenstein, this webinar will help you move from speculation to a concrete plan. 

A few key takeaways you can expect: 

• a clear view of whether you need to register and what you must submit, 

• an understanding of how swissdamed and EUDAMED relate (and where they don’t), and 

• a practical preparation roadmap you can use to align stakeholders and stay on track for 2026. 

Register via the form to secure your seat!