Vice President of Regulatory Affairs
Ms. Louise Peltier is a regulatory affairs professional with over 30 years of hands-on, multidiscipline experience with pharmaceuticals, biologics and in-vitro diagnostics. Her expertise spans the American, Canadian, and European registration processes, from beginning to end, including direct agency interactions.
She has developed regulatory strategy at all stages of development for therapeutic biologics, in-vitro diagnostics and new chemical entities for both American and European registrations. She was most recently the Senior Director of Regulatory Affairs for Phamathene. Prior to that role, she held similar positions at Caris Life Sciences and Northwest BioTherapeutics.