##  [Medical Devices in the UK & UKCA Certification Readiness](/webinars/medical-devices-in-the-uk-ukca-certification-readiness) 

<a>Medical Devices</a>



<a>Past Webinar</a>



## **Medical Devices in the UK &amp; UKCA Certification Readiness**

**The webinar was successfully concluded on**

  **May 25, 2022.**





We are pleased to see your interest in Freyr’s Webinar Series (FWS). The webinar on “**Medical Devices in the UK &amp; UKCA Certification Readiness”** was successfully concluded on May 25, 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 Here is an archived version of the session for your perusal.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 Igor Dorosh, Associate Director - Business Development - Europe &amp; Africa have discussed the below aspects.

- UK Medical device Regulations- Introduction
- What is UKCA Marking?
- Routes for Compliance to UKCA Marking
- Timelines for UKCA Marking
- The UK Approved Bodies
- Impact for Manufacturers – UK &amp; Non-UK
- Next Steps for Manufacturers
- Q&amp;A

As a continuous practice, Freyr is destined to organize more on-demand webinar sessions related to Regulatory aspects of Life Sciences. We presume that you would like to be a part of it. If yes, let us have an opportunity to inform you about our next session.