Laura Huffman MS U.S. FDA

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Laura Huffman MS U.S. FDA CVM Pre-Approval Facilities Assessment Program, Lead, ONADE, CVM

Laura Huffman joined the FDA in 2004 and is currently leading CVM's Pre-Approval Facilities Assessment Program in the Division of Manufacturing Technologies (DMT), Office of New Animal Drug Evaluation at CVM. Her roles include facilities assessment, pre-approval inspection and mutual recognition policy for CVM. Prior to joining the FDA, Laura worked in regulation and manufacturing of food and biologics. Previously she served as a Master Microbiology Reviewer in the area of sterile drug review in DMT. Laura received a Bachelor of Science in Biology and a Master of Science in Food Science and Technology, both with microbiology focus, from Virginia Tech.