Swixit - Regulatory Impact for Medical Devices & Med Tech Industry
The webinar was successfully concluded on
March 23, 2022.
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 Here is an archived version of the session for your perusal.
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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.