Eva Caruso is a Senior Project Manager and Regulatory Affairs Specialist at MCRA Japan, an IQVIA business. Since joining MCRA Japan in April 2023, Eva has specialized in assisting foreign manufacturers with navigating the PMDA regulatory process while aligning PMDA requirements with FDA and EU MDR standards. Previously, Eva held roles at MCRA, LLC, and Organoid Therapeutics, focusing on cardiovascular regulatory affairs and quality assurance activities. Eva earned a Master’s in Medical Product Engineering from the University of Pittsburgh and a Bachelor’s in Bioengineering from Clemson University.
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