Sarah Smith, MS
Associate Director
Sarah is a regulatory operations professional with experience in drafting, formatting, and publishing electronic submissions for filing to FDA. She is responsible for ensuring that regulatory submissions to FDA are appropriately published according to relevant guidances and free of technical issues. Sarah also has experience performing Quality Control reviews of documentation for the nonclinical, clinical, and chemistry, manufacturing, and control practice areas of SciLucent. Sarah has a B.S. in Biology from James Madison University and an M.S. in Biology from Towson University.
