Patricia Setti-LaPerch is a seasoned professional in regulatory affairs with extensive experience in the medical device and healthcare sectors. Currently serving as the Senior Director of Regulatory Affairs at RapidAI since October 2022, Patricia previously held the position of Director of Regulatory Compliance and Quality at Koios Medical, where Patricia successfully implemented SaMD eQMS and obtained multiple certifications with zero findings. Prior roles include Senior Associate Director of Medical Devices at Bayer, focusing on regulatory strategy for consumer device product lines, and Manager of Regulatory Affairs at Stryker, where Patricia led a large team in supporting a substantial SKU portfolio and played critical roles in product commercialization and international regulatory efforts. Patricia holds a Master’s degree in Biomedical Engineering from Columbia University and a Bachelor’s degree in Engineering from The Cooper Union for the Advancement of Science and Art.
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