Drug Interactions Expert Witnesses

drug interactions expert testimony

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Drug interactions expert witness candidates typically have a PhD with areas of expertise in pharmacokinetics, clinical pharmacology, internal medicinemicrobiology, and/or are board certified registered pharmacists (RPh). In a high-profile case, or litigation involving a significant financial stake, a law firm may request a drug interaction professional with prior expert testimony experience. Experts may be a member of an industry association such as the Pharmaceutical Research and Manufacturers of America (PhRMA), or the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA).

The process of drug development – from concept, preclinical testing, clinical trial development to an approved drug – typically takes more than 10 years. Drug interaction science is a key component of drug development, identifying change in the effects of drugs or side effects of a drug when administered with a food, beverage, supplement, or another drug.

Litigation support by drug interactions expert witness could involve intellectual property matters such as a patent litigation or a trade secret dispute. Wrongful death, standard of care, product liability, and medical malpractice cases could also require the expertise of a drug interactions expert. Expert witness services by an expert specializing in drug interaction could include expert report preparation, expert opinion, depositions, and expert witness testimony at a trial. In addition, a law firm may request a toxicologist or pharmaceutical industry expert for pre-litigation consulting work. Representing the plaintiff or defendant, top litigation firms call on Cahn Litigation Services to find medical expert witnesses for a wide variety of matters including cases involving:

Cahn Litigation Services has many years of experience providing pharmacology experts and toxicology experts with the right balance of expertise and testimony to get the job done.

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Drug Interactions Expert Witness - Representative Bios

Please Note: All Cahn Litigation expert witness searches are customized to attorneys' precise specifications and preferences. Attorneys are encouraged to discuss search parameters with a Cahn search specialist.

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The below expert witness bios represent a small fraction of those Drug Interactions experts known by Cahn Litigation Services. These bios are provided to give lawyers a sense of the Drug Interactions landscape.

Expert Witness #211083

This expert’s research interests include pre-clinical and clinical studies on drug metabolism, transport and pharmacokinetics. The current focus of this expert’s laboratory is on the regulation of drug-metabolizing enzymes and its relevance to clinical pharmacology of anti-cancer and antiretroviral drugs. This expert has significant experience in pharmaceutical R&D, and expertise in scientific, regulatory, and intellectual property issues pertaining to drug discovery and development. This background has allowed this expert to serve as a consultant/expert witness for various patent litigation issues that involve pharmaceutical formulations (immediate release and sustained/controlled release), pharmacokinetics, pharmacodynamics, drug metabolism, drug-drug interactions, and bioequivalence. This expert has worked on behalf of both plaintiff and defendant for patent infringement cases filed by the innovator or generic drug companies. This expert is an active member of several organizations including American Association of Pharmaceutical Scientists. This expert also serves as a member of an Experimental Therapeutics Study Section for Department of Defense Breast Cancer Research Program.

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Expert Witness #258337

This expert is Chair of a Department of Chemical Engineering. This expert was trained in Controlled Release and Drug Delivery and has become a widely recognized expert in the field. This expert has many years of experience as an expert witness and consultant in Hatch-Waxman and Product Liability Litigation and has focused on many ANDA matters, specializing in the fields of Chemical Engineering, Pharmaceutical Science and Bioengineering with unique expertise in the areas of Small Molecule and Biologics Pharmaceutical Formulation, Controlled/ Extended/Sustained/Delayed Release, Excipient and Biomaterials Function/Interaction, Formulation Characterization and Formulation Testing. This expert has published over 85 peer-reviewed articles on Pharmaceutical Science and has received numerous elite national and international awards and accolades for research and teaching. This expert has testified on Controlled Release, Pharmaceutical Formulations, Biomaterials, and Biodegradation including serving as the omnibus expert witness on both infringement and validity simultaneously, as Markman expert witness, a testing witness, an expert designated to give a tutorial to the jury, and also an expert consulting on matters (including legal strategy) at the District Court, Federal Circuit, and even aiding council for cases heard at the Supreme Court level.

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Expert Witness #256020

This expert brings to the table many years of pharmacy management, ownership and advisory experience and expertise. This expert holds a B.S. in Pharmacy and is a Registered Pharmacist. This expert is a Master Senior Appraiser and Real Estate Broker, has been a Member of a State Board of Pharmacy and a Commissioner for a Department of Licensing & Regulation.

As president of a highly successful Pharmacy Advisory, this expert regularly consults with and advises owners and managers of Pharmacies and individual pharmacists regarding professional and management practices and procedures in retail pharmacies. These include:

-  Receipt, handling and maintenance of prescriptions and prescription records;
-  Prescription interpretation and assessment activities;
-  Confirmation that the drug product dispensed is the same as the drug product ordered;
-  Patient counseling as needed before final delivery of filled prescription order.

As the owner and/or manager of 10 different retail pharmacies, this expert speaks from experience and with authority when consulting on topics such as:

-  Interactions with governmental and licensing agencies/regulatory boards;
-  Supervising/performing financial functions, such as budgeting, cash flow analysis and monitoring business financial status;
-  Accountability for regulatory compliance with federal and state laws and rules pertaining to the purchase, storage, security and expiration status of controlled substances and dangerous drugs;
-  Supervision of and calculations for third party audits and contract responsibilities (e.g., for Medicaid and other third-party payor programs);
-  Market analysis, staffing, planning & budgeting;
-  Public relations, management program development, and lobbying efforts in support of pharmacy profession.

This expert has extensive expert witness experience, serving equally for the plaintiff and the defense. This expert has written reports, been deposed and testified.

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