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.
July, 2020 - present
Regulatory Affairs Specialist at NICO.LAB
Regulatory Affairs Specialist at FoodScience, LLC
Regulatory Affairs Specialist at Suterra
Regulatory Affairs Specialist at Meditrial
Regulatory Affairs Specialist at MIS Implants Technologies Ltd. (Global)