Drug Development Expert Witness 523160


Expertise Description

I have over 35 years experience in the fields of toxicology, pharmacology, pharmacokinetics and drug development. My expertise includes global nonclinical development of small molecule and protein drugs, regulatory toxicology (FDA, EU and Japan), performing due diligence on potential inlicensed programs, conducting inhouse and contract GLP pharmacology/toxicology/ADME/PK studies, in vitro toxicity testing and screening, in vivo disease models, research and investigational toxicology, assessment of immunotoxicologic/host resistance/hematopoietic effects of drugs and chemicals, flow cytometry, pulmonary toxicology/immunology and biosimilars. I am offering my services as a drug development expert witness.

Areas of Expertise


Education

Degree Subject Institution
Ph.D. Pharmacology/Toxicology/Immunotoxicology Medical College of Virginia – Richmond Virginia
B.S. Biology/Chemistry Bucknell University – Lewisburg Pennsylvania

Licenses Certifications

Certification:
Diplomate of the American Board of Toxicology
Member of the Board of Directors for the American Board of Toxicology
President of the Board of Directors for the American Board of Toxicology

Awards & Affiliation

Society of Toxicology: Immunotoxicology specialty section, Regulatory and Safety Evaluation specialty section, Drug Discovery specialty section
American College of Toxicology
Round Table of Toxicology Consultants


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