Abby Brehm

Abby Brehm is a Senior Regulatory Scientist at Voisin Consulting Life Sciences (VCLS) since August 2017, with extensive experience in the preparation and submission of Clinical Trial Applications in Europe, managing project timelines and budgets, and providing regulatory guidance to clients. Prior to VCLS, Abby served as a Regulatory QA Specialist for Cell Therapies at Dana-Farber Cancer Institute, where responsibilities included IND/IDE submissions to the FDA and coordinating internal audits. Abby's earlier roles include Quality Assurance Co-op at Cambridge Biomedical Inc., Medical Technologist positions at Tufts Medical Center and Northwestern Memorial Hospital, and research contributions at institutions like the US Environmental Protection Agency and Cincinnati Children’s Hospital. Abby holds a Master of Science in Biopharmaceutical Regulatory Science from Northeastern University and a Bachelor of Science in Clinical Laboratory Science from the University of Cincinnati.