Caroline Mendes is a seasoned professional in regulatory affairs and biotechnology, with extensive experience in the development of diagnostics and therapeutic solutions. At Abbott, Caroline held positions as Regulatory Affairs Manager and Principal Regulatory Affairs Specialist from March 2022 to August 2025, focusing on new product development and pre-market submissions for in vitro diagnostic devices, including FDA submissions. Prior roles include Senior Regulatory Affairs Specialist and Technologist at Instituto de Biologia Molecular do Paraná, where evaluations of antigen and antibody sensitivity and specificity were conducted for diagnostic kits for infectious diseases. Academic achievements include a PhD in Biological Sciences from Technological University Dublin, where research centered around a targeted drug delivery system for cancer therapy, alongside undergraduate research experiences in microorganism characterization and infectious disease diagnostics development at Pontifícia Universidade Católica do Paraná.
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