Rachel C. Thomson

RACHEL THOMSON advises pharmaceuticals, biologics, and medical device clients on a variety of regulatory compliance and enforcement matters, applying her valuable practical experience in these FDA-regulated sectors.

Rachel graduated from the Catholic University of America’s Columbus School of Law. She has extensive industry experience in quality and regulatory compliance at various global healthcare companies. She has led remediation activities at pharmaceutical and biologics manufacturing sites within the U.S. and abroad, including preparing responses to inspectional observations, development of CAPA plans, GMP auditing, and inspection readiness.

Before joining Sidley, Rachel was the Executive Director for a pharmaceutical consulting firm where she provided experienced GxP compliance consulting to domestic and international clients in pharmaceutical and biotech manufacturing.

Rachel holds a B.S. in biology from University of New Hampshire.