Swiss Medtech Webinar

Swiss importers: Are you ready for the 2025 Swissmedic inspection?

Swissmedic has launched a market surveillance campaign and has informed all registered Swiss importers of medical devices and in vitro diagnostics that it will inspect compliance with the Ordinances on Medical Devices and In-Vitro Diagnostics in 2025. A failed inspection poses a significant risk to your business.

Don’t leave your success to chance. In Swiss Medtech’s exclusive webinar, you will learn how to prepare a Swissmedic inspection. Gain firsthand insights from HUBERLAB. AG, a Swiss importer that has successfully navigated a Swissmedic inspection. Together with the regulatory experts from Decomplix AG, they will share invaluable tips, best practices, and lead you through the process.

In this webinar, you will discover:

• How a Swissmedic inspection really works – based on a real-world case.
• Proven best practices to ensure compliance.
• Common pitfalls and how to avoid them.
• Answers to your most urgent questions – please submit them during registration.
  
   

Target group

The Swiss Medtech Webinar is aimed at all interested Swiss importers who want to prepare for a Swissmedic inspection: Owners, board members, executives, and regulatory managers who want to safeguard their well-run business and confidently face any regulatory challenge in Switzerland. The event will be offered in English on 03 july. It is free of charge for members of Swiss Medtech. All other interested parties can register for a fee of CHF 60. 

Registration

The webinar will be recorded and published on this page approx. 7-10 days after the event.

Programm

Registration