Erik Larsen, GLP Compliance Auditor

Specialties: Regulatory, Manufacturing

Erik Larsen

Erik Larsen is a Quality Assurance professional with over 39 years of industry experience in Pre-Clinical Toxicology and Bioanalytical Systems, GLP & GCP Systems including Animal Health, Animal Welfare Compliance, and Quality Systems implementation.

Mr. Larsen’s experience includes managing and working with teams of professionals across multiple sites including EU and Japan. His experience includes audits in over 15 countries and multiple GxP disciplines (e.g., GLP, GCP, GCPV) focused on regulatory inspections, agencies, and global submission requirements and applications.

Prior to becoming a consultant and auditor, Mr. Larsen worked at Pfizer as the Director of Research & Development Oversight (RDO), and prior to that as the Associate Director/Director; Global Strategic Initiatives (GSI). Before joining Pfizer, he worked in R&D and held leadership QA roles at Upjohn, Pharmacia and Upjohn, and Pharmacia.

Mr. Larsen received his M.A. in Physiology/Biology and his B.A. in Biology, Chemistry, Environmental Sciences from Western Michigan University.