Lesley Reeve, PhD, MSc Reg Aff
Senior Director, Nonclinical Regulatory Strategy
Lesley is a Senior Director of Nonclinical Regulatory Strategy within Fortrea’s Product Development and Market Access Consulting team. She brings nearly 30 years of experience providing scientific and regulatory guidance on the nonclinical development of drugs and medical devices, including small and large molecules, ATMPs, impurities and excipients. Her experience includes nonclinical data review, study package design, due diligence and in-licensing support, authorship of expert nonclinical documents, and regulatory agency interactions.
Lesley is a highly regarded regulatory professional and a Fellow of TOPRA and the British Toxicology Society (BTS), as well as an Industrial Fellow of the University of Hertfordshire. She is actively involved in scientific committees and regulatory education, serving since 2010 as Module Leader for the Nonclinical Module of the TOPRA MSc in Regulatory Affairs.
She holds a PhD in Genetics from the University of Leeds and an MSc (with Distinction) in Regulatory Affairs from Cardiff University and TOPRA.