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Animal Science

These Animal Science expert witnesses are experts in this Pharmacology Industry Expert Witnesses for Attorneys directory that provide independent court testimony or as consultants by review of records and verbal or written report. They provide expert testimony at deposition or trial in the area of Animal Science. The following list contains testifying experts with specific Pharmacology Industry Expert Witnesses for Attorneys background to Animal Science. To setup a screening with our experts simply choose the request this expert button located in the experts information pageConsolidated Consultants has referred Pharmacology Industry Expert Witnesses for Attorneys Animal Science expert witnesses to both Plaintiff and Defense attorneys for many years. Please review the wide variety of Animal Science expert witnesses and use the request this expert option to contact us.

1. Pharmaceutical Development Scientist Expert Witness

Provides Opinion & Testimony In:

Pharmaceutical Scientist, Pharmaceutical Consultant, Hatch Waxman, Pharmaceutical patent litigation, CMC Development issues, Preformulation, Pharmaceutics, GMP Operations, Polymorph, Formulation Development, Drug Delivery, Due Diligence, IND NDA, SOPs

2. Toxicology Pharmaceutical Chemical Exposure Expert Witness

Provides Opinion & Testimony In:

Toxicology, Toxicology, Pharmaceutical, Chemical Exposure Causation, Solvents, Butadiene, Phenylpropanolamine, Metabolism, Biotransformation, MSDS, Cancer, Drugs, Malpractice, Overdose, Prescriptions, Poison, Poisoning, Toxicologist, Dust Exposure, Stem cell, Industrial Hygiene, Air sampling, Occupational exposure pharmaceuticals, Occupational exposure chemicals, Occupational exposure solvents, Occupational exposure limits OELs, Drug related malpractice, Industrial hygiene, Environmental compliance, Hazard communication, Toxicological causation, Chemical exposure, cancer, Potent pharmaceutical compounds, Pharmaceutical impurities, toxicity, Pharmaceutical product exposure, Dust explosion risks, Air purification system, Design implementation of an effective potent compound program, Lithium drug interaction resulting in toxicology, Potency categorization, Industrial hygiene monitoring, Reproductive toxins in the workplace, Residual solvent level justification, Excipient levels above the FDA inactive ingredient guideline justifications, Environmental reporting for SARA, Biennial hazardous waste reporting,

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