Dan Kim is a Regulatory Affairs Specialist at SAM Medical, with experience in managing international registration of medical devices and UDI implementation. Dan has a strong background in EU MDR requirements, risk management, post-market surveillance, and clinical evaluation. Prior to this role, Dan worked as a Regulatory Affairs Associate at BioFire Defense and as a Product Development Engineer at Bench to Bedside. Dan also has experience in biomedical research and UI design. Dan holds a Bachelor's degree in Biomedical/Medical Engineering from the University of Utah.
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