##  [EUA and Post-EUA Regulatory Journey of Medical Devices](/index%2ephp/webinars/eua-and-post-eua-regulatory-journey-of-medical-devices) 

<a>Medical Devices</a>



<a>Past Webinar</a>



## **EUA and Post-EUA Regulatory Journey of Medical Devices**

**The webinar was successfully concluded on**

  **August 12, 2020.**

[Download Webinar](javascript:void(0))





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.