DABT - Diplomate American Board of Toxicology, DACVP - Diplomate American College of Veterinary Pathologists
Kansas State University BS 1971 Kansas State University DVM 1973 Kansas State University PhD 1978
Biologics/Biotherapeutics/Biotechnology, Carcinogenicity, Cardiovascular Toxicology, Drug/Pharmaceutical Development, GLP Study Auditing, Hematologic Toxicology, Hepatic Toxicology, Product Safety Assessment, Regulatory Toxicology, Renal Toxicology, Toxicologic Pathology
Nonclinical pharmaceutical product development/In-licensing and out-licensing product managment/Risk assessment/Pathology peer review/Pharmaceutical toxicology
Thirty-five years of pharmaceutical research and product development experience. Pharmaceutical product development experience includes project team management of early stage pharmaceutical portfolios, preclinical pharmaceutical development and in-licensing and out-licensing product management. Extensive experience in developing preclinical and proof-of-concept development programs for virtual and small pharmaceutical companies. Extensive FDA interactions in support of pre-IND, IND and NDA submissions. Academic career included technology transfer negotiations, development of a center of excellence, foundation development leadership and academic-industry liaison.
13300 E. Via Linda #1041