##  [Medical Devices in UK & UKRP: Guidance for Non-UK Manufacturers](/index%2ephp/webinars/medical-devices-in-uk-ukrp-guidance-for-non-uk-manufacturers) 

<a>Medical Devices</a>



<a>Past Webinar</a>



## **Medical Devices in UK &amp; UKRP: Guidance for Non-UK Manufacturers**

**The webinar was successfully concluded on**

  **August 4, 2021.**

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We are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on, **“Medical Devices in UK &amp; UKRP: Guidance for Non-UK Manufacturers”,** was successfully concluded on August 4, 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 Here is an archived version for your perusal.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, Director - Medical Devices and Igor Dorosh, Associate Director - Business Development - Europe &amp; Africa discussed the following points in the session:

- Regulatory Overview for Medical Devices &amp; IVDs in the UK
- Post-Brexit UK MHRA Requirements for Medical Devices
- Registration Timelines with the MHRA for Class IIa, IIb and I Devices
- Regulatory Updates for Class III Devices Post-Brexit Transition Period
- UKRP - Roles and Responsibilities
- Success Stories/Case studies
- Q&amp;A Session

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.