Sarah Smith, MS
Associate Director
Sarah is an experienced regulatory operations professional whose expertise includes coordinating, publishing, and transferring 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 is also responsible for ensuring the completeness, quality, and proper validation of submissions. She has managed the publishing and submission of over 2,000 regulatory submissions at SciLucent. Sarah has a B.S. in Biology from James Madison University and an M.S. in Biology from Towson University.
