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.