Sarah Mollo FDA

Sarah Mollo serves as Biocompatibility Consultant and Lead Reviewer in the General Hospital Device Branch in CDRH’s Office of Device Evaluation. Within the Agency, Sarah serves as the Agency’s standards liaison for over multiple international standards, is part of the team developing three device specific guidance documents, and sits on the Biocompatibility Policy Forum. Prior to joining the FDA, Sarah was a post-doc at Harvard University. Sarah earned her bachelor’s in Microbiology and Cell Science from the University of Florida and her doctorate in Immunology from the University of Alabama at Birmingham.