About me
Sarah Fairfield is a dedicated and passionate regulatory professional with extensive expertise in medical devices and combination products. Currently, she serves as the Associate Director of Regulatory Affairs at AbbVie, Inc., where she supports global product development. She also manages software as a medical device (SaMD) and digital health technologies (DHT), advocating for their critical adoption in clinical trials. She earned her MBA from Boston University, a B.S. in Biomedical Engineering from Purdue University, and a RAC US Certification.
