##  [Medical Devices in the UK & UKRP: Latest Industry Updates](/webinars/medical-devices-in-the-uk-ukrp-latest-industry-updates) 

<a>Medical Devices</a>



<a>Past Webinar</a>



## **Medical Devices in the UK &amp; UKRP: Latest Industry Updates**

**The webinar was successfully concluded on**

  **October 27, 2021.**





We are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on “**Medical Devices in the UK &amp; UKRP: Latest Industry Updates”** was successfully concluded on October 27, 2021. Here is an archived version of the session for your perusal.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 expert, Nisha Vempalle, Director - Medical Devices, elaborated on:

- Introduction to Regulatory Landscape in the UK
- Overview of the MHRA Registration Timelines
- MHRA Regulatory Updates Post September 1, 2021, Timeline
- Import Obligations of UKRP
- Do You Need Importer/Distributor?
- Dos and Don’ts for a UKRP
- Certificate of Free Sales for non-UK manufacturers
- Post Registration Activities for Manufacturers &amp; UKRP
- UKRP Challenges from Practical Scenarios
- Success Stories/Case Studies

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.