Expert Profile |
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With over 50 years of experience this pharmacology expert has studied the interactions that occur between a living organism and chemicals that affect normal or abnormal biochemical function. He specializes in the discovery and development of drugs for cardiovascular disease. His experience and expertise include drug research and regulation. After 12 years of experience in the pharmaceutical industry, he joined the Food and Drug Administration (FDA) as a Deputy Director of the Division of Cardiorenal Drugs. His responsibilities included the review, evaluation, and approval of new drugs and blood substitutes as well as Tissue Plasminogen Activator (TPA). He has 10 years of consulting experience in the cardiovascular area and other disciplines regulated by the FDA. He has experience in drug development and conducts clinical trials. He is currently consulting on areas such as AIDS, antidepressants, cardiovascular, endocrine, biotechnology products, wound healing, and anticancer drugs, among others. He has extensive experience with generic drugs and over the counter drug evaluation.
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Expert Witness Experience
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- Consulting for litigation support
- Testified in deposition and at trial
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Industry Experience
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- Responsible for preclinical toxicology at the FDA
- Multiple professional memberships in organizations such as American Association for the Advancement of Science American College of Cardiology, American Heart Association, and American Society for Clinical Pharmacology, among others.
- Authored and co-authored over 30 professional publications
- Worked on product liability and labeling issues
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Educational Background
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- Post-doctoral Fellowship, Pharmacology
- Ph.D., Pharmacology
- M.S., Pharmacology
- M.S., Pharmacology
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