Clinical Trials Expert Witness


Clinical trials expert witnesses and consultants listed here may be able to form expert opinions, draft expert witness reports, provide expert witness testimony at deposition and/or trial as or serve as consulting (non-testifying) experts on clinical trials. The clinical trials expert witness listings on this page are typically from fields/areas of expertise such as: Infectious Diseases, Nutrition, Pharmaceutical Regulation, Pharmacist, Pharmacology- Clinical, and Sports Medicine.

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Anthony L. Almada, MSc

Dana Point, California
Nutrition, Sports Medicine - Dietary Supplements, Nutraceuticals, Sports Nutrition, Protein, Cosmetics, Energy Drinks, Caffeine, Stimulants, Banned Substances, Doping, Cannabinoids, Hemp Extracts, Cannabidiol / CBD, Probiotics, Weight Loss, Pet Supplements, Clinical Trials, Clinical Research, Botanical / Herbal Extracts
Forty-six years of natural products industry experience, including co-founder of several dietary supplement, sports nutrition, and cosmetic companies; creator of "thermogenic" / weight loss category (in 1990); co-creator of creatine category in North America (1993). Zealous, evidence-based scientist (nutritional and exercise biochemist), with collaborations on over 50 university-based clinical trials, ranging from AIDS to Lou Gehrig's disease to muscle building to weight / fat loss. Internationally recognized as evidence-based communicator and leader. Interviewed in NY Times (page 1a), Forbes, and Business Week. Savvy and experienced in trademark / trade dress and patent infringement (studied for the US Patent Bar), including expert witness engagement. Past expert in CBD and Cannabis / hemp extracts, misbranded cosmetics, energy and cognitive function drinks, violation of GMPs in manufacturing /adulterated products, and doping violations of elite/pro athletes linked to dieta...

Gourang P. Patel, Pharm.D Critical Care Education

Inverness, Illinois
Pharmacology- Clinical, Pharmacist - Medication, Error, Toxicology, Adverse Drug, Pharmacology, Clinical Trials, Pharmacy, Critical Care, Intensive Care Unit, Prescription, Prevention, Operating Room Medication Safety
Specialization of pharmacology and toxicology of medications utilized both in the hospital and retail pharmacy settings. Detailed analysis of medication errors, adverse drug reactions, and providing strategies for prevention. Particular focus on practice of pharmacy, medication side effects, and medication safety.

David B Ross, MD, PhD, MBI

Baltimore, Maryland
Pharmaceutical Regulation, Infectious Diseases - Food and Drug Administration (FDA), drug/biologics safety/labeling/post-marketing surveillance, FDA drug/biologics regulations/procedures/applications (INDs/NDAs/BLAs), clinical trials, drug development, pharmacy compounding, HIV, MRSA, antibiotics, hepatitis, osteomyelitis, influenza, C. difficile
Dr. Ross is a Yale fellowship-trained, board-certified infectious disease physician. An active clinician in practice for over 25 years, he provides patient care in the areas of infectious disease and primary care. Dr. Ross holds a medical degree from New York University School of Medicine, and an undergraduate degree in Molecular Biophysics and Biochemistry from Yale University. He completed his internal medicine residency training at NYU Medical Center, and infectious disease fellowship training at Yale University. Dr. Ross also holds a M.S. and Ph.D. in Biochemistry from NYU, and a Master’s Degree in Biomedical Informatics from Oregon Health and Sciences University. Dr. Ross spent 10 years with the FDA’s Center of Drug Evaluation and Review (CDER) as a medical officer, senior medical reviewer, medical team leader, and new drug review office management official. He has extremely broad experience with FDA regulatory submissions (INDs, NDAs, BLAs, post-marketing safety, labeling ...