We are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on “Swixit - Regulatory Impact for Medical Devices & Med Tech Industry” was successfully concluded on March 23, 2022. Here is an archived version of the session for your perusal.

What Was It All About?

In this webinar, our in-house Regulatory experts – Nisha Vempalle, Director - Medical Devices and Dr. Ceren Alemdaroglu- Regulatory Affairs Specialist (PRRC), Medical Devices, elaborated on:

• Overview of Swixit and Swiss Medical Device Regulations
• Routes to Market in Switzerland
• Overview of Swiss AR and Roles
• PRRC - Roles and Responsibilities
• Labeling Requirements
• Key Implications
• Case Study
• Live Q&A

As a continuous practice, Freyr is destined to organize more webinar sessions related to Regulatory aspects of Life Sciences. We presume that you would like to be a part of all the upcoming sessions. If yes, let us have an opportunity to inform you about our next session.