Gabrielle Zaeska, Vice President of Regulatory Affairs & Quality, is an established Regulatory Affairs leader with over 15 years of experience in the medical device industry. Her expertise includes executing regulatory strategy and submissions for the US, EU, and Canada markets, as well as supporting new product applications globally (Australia, Asia, Latin America). Gabrielle began her career in biocompatibility before transitioning into Regulatory Affairs where she formerly led teams at St. Jude Medical and Abbott Laboratories within the Structural Heart divisions. She has also served as a working group member of the International Organization for Standardization (ISO) creating a standard for cardiac occluder devices. Gabrielle received a M.Sc. in Regulatory Affairs from St. Cloud State University and a B.S. in Biology from the University of Minnesota.

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