Allison Lenihan, MPS

Allison is a clinical development and regulatory affairs professional focused on supporting the advancement of healthcare products. She is involved in the preparation and coordination of clinical materials for regulatory submissions, including Investigational New Drug Applications (INDs) and New Drug Applications (NDAs), across multiple therapeutic areas. She is also involved in performing data quality reviews of submissions to ensure accuracy and compliance. Allison’s background includes work in regulatory affairs and early-stage drug development, with a focus on oncology programs.  Allison has an M.P.S. in Regulatory Science from the University of North Carolina and a B.S. in Marine Biology from the University of North Carolina.