##  [Post Brexit Scenario for Medical Devices: Appointing a UKRP](/index%2ephp/webinars/post-brexit-scenario-for-medical-devices-appointing-a-ukrp) 

<a>Medical Devices</a>



<a>Past Webinar</a>



## **Post Brexit Scenario for Medical Devices: Appointing a UKRP**

**The webinar was successfully concluded on**

  **April 21, 2021.**

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We are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on, **“Post Brexit Scenario for Medical Devices: Appointing a UKRP”,** was successfully concluded on April 21, 2021. Here is an archived version for your perusal.

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#### What Was It All About?

In a nutshell, our in-house Regulatory experts - Nisha Vempalle and Igor Dorosh discussed the following points in the session.

- Overview of the UK Medical Devices Market
- Overview of the MHRA
- Routes to Market the Medical Devices in Britain and Norther Ireland (NI)
- Who is a UKRP?
- Roles and Responsibilities of a UKRP
- Solutioning Models

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 those sessions. If yes, let us have an opportunity to inform you about our next session.