Jenny Chan, RAC, PMP, is an Associate Director of Regulatory Affairs at Abbott, specializing in complex medical devices with extensive experience in FDA Class III PMAs and Class II 510(k)s, as well as EU MDR/AIMD/MDD regulations. They have held roles at St. Jude Medical and Boston Scientific, focusing on neurostimulators and advanced heart failure management technologies. Jenny earned a BS in Biomedical Engineering and an MS in Regulatory Science from the University of Southern California, along with a Certificate in Project Management and completed the RAPS Executive Development Program at Northwestern University.
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