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
