##  [Swixit - Regulatory Impact for Medical Devices & Med Tech Industry](/index%2ephp/webinars/swixit-regulatory-impact-for-medical-devices-med-tech-industry) 

<a>Medical Devices</a>



<a>Past Webinar</a>



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 Here is an archived version of the session for your perusal.

#### Get Your Copy of ROW Recording

[Download Webinar](javascript:void(0))









#### Get Your Copy of AMR Recording.

[Download Webinar](javascript:void(0))













 

#### 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&amp;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.