Jarrett Boyd, MS

regulatory affairs specialist

Jarrett Boyd is a recent graduate of Carnegie Mellon University where he finished his Master of Science in Biomedical Engineering. He has three years of experience developing medical devices for a wide range of applications including cardiovascular systems, assistive technology, and infectious diseases. Through these projects, he has experience with FDA reports, risk analysis, intellectual property, and reimbursement. He also has direct experience serving as a project lead for several teams of graduate students mentoring them through the medical device creation process in accordance with ISO 13485.

While studying at Carnegie Mellon University, Jarrett also focused on the utilization of artificial intelligence within the biomedical field. He has experience employing and writing several different machine learning and deep learning algorithms as well as evaluating their effectiveness. His research at CMU saw the application of molecular dynamic simulations for a wide variety of biomedical applications. Including detection and classification of nucleotides and evaluations of activation efficiency of G-protein coupled receptors.

For more information, please see his LinkedIn Profile.