Medical Devices
Past Webinar

EUA and Post-EUA Regulatory Journey of Medical Devices

The webinar was successfully concluded on

August 12, 2020. 

Download Webinar

We appreciate your interest in Freyr’s Webinar Series. Our recent webinar on “EUA and Post-EUA Regulatory Journey of Medical Devices”, was concluded successfully on August 12, 2020.

What Was It All About?

In a nutshell, during the webinar our Regulatory experts, Kristen Laudicina, Client Partner and Meenakshi Verma, Team Lead, Medical Devices discussed and shared their insights on:

  • Regulatory Framework for Emergency Use Authorizations (EUAs) in the U.S.
  • Device Categories That Qualify for an EUA
  • Procedure for Obtaining EUA, Validity and Conditions Of EUA
  • Post-EUA Regulatory Action Plan and Transition to Device Approval for Long Term Marketing Continuity

As a continuous practice, Freyr is destined to organize more webinar sessions related to Regulatory aspects of Life Sciences. We are sure you would like to be a part of all those sessions. If yes, we will be happy to inform you in prior about our next session.