Drug expert witnesses evaluate the development, labeling, prescribing, and monitoring of medications, as well as adverse drug events and interactions. Drawn from pharmacology, pharmacy, toxicology, and clinical practice, they analyze compliance with standards of care, FDA regulations, risk management protocols, and institutional medication-use systems.
Oncology Drug Discovery & Development Expert Witness
Oncology Drug Discovery & Development Expert Witness
- Review Fee
- $500/hr
- Deposition Fee
- $500/hr
- Court Fee
- $500/hr
This highly experienced expert in drug discovery and drug development earned his PhD in Pharmacology from Yale University and thereafter completed a postgraduate fellowship at the University of Michigan. He previously served as the Chief Scientific Officer of Adherex Technologies, International Vice President of Cancer Research at Glaxo Wellcome (now GSK) and Associate Division Director of Experimental Therapy at Burroughs Wellcome. He is a member of the American Chemical Society, the American Association for Cancer Research, and the American Society of Clinical Oncology. He has extensive experience in preclinical and clinical research and legal consulting.
President, An Independent Pharmaceuticals Consultancy
Doctor of Philosophy (PhD), Yale University
Chapel Hill,
North Carolina