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.