Crossing the eSTAR Chasm: Transitioning to FDA’s Mandatory 510k eSTAR Submission Process by October 2023

This webinar will educate and prepare medical device manufacturers, regulatory affairs leaders, and regulatory consultants to effectively transition their processes, resources, and operations to seamlessly adopt the eSTAR as the new submission standard. This session will share watchouts, best practices, and tips and tricks to adapt to eSTAR.