FDA Approval Expert Witnesses in Rhode Island

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FDA approval expert witnesses practice in a variety of fields, including pharmaceuticals, medical devices, food safety, biotechnology, and clinical trials. Some of the most common FDA approval expert witness specialties also include drug labeling, dietary supplements, cosmetic products, veterinary medicine, and tobacco products. They can opine on the effects of regulatory compliance, product recalls, adverse event reporting, post-market surveillance, and risk management.

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Family Medicine Expert WitnessView profile

E-158437

Family Medicine Expert Witness

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Rhode Island

This expert earned his BS from Brown University and his MD from Brown University's Alpert Medical School; following this he went on to complete a family medicine residency at the Memorial Hospital of Rhode Island. He is active in his field as a member of professional organizations such as the American Academy of Family Physicians and the Society of Teachers of Family Medicine. His expertise are...

Chemistry and Pharmaceuticals Expert WitnessView profile

E-528687

Chemistry and Pharmaceuticals Expert Witness

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Rhode Island

This highly-qualified expert in chemistry and pharmaceuticals has 20 years of experience in his field. He has experience with analytical chemistry analysis, formulation chemistry, and FDA regulation, and his work has involved in all aspects of drug research and development from synthesis/purification, in-vitro, in-vivo (efficacy, pharmacokinetics and pharmacodynamics) testing, dosing routs, drug...

FDA Approval Expert Witness FAQs

An FDA Approval expert witness provides insight on regulatory compliance, drug approval processes, and medical device clearance. They can testify on whether proper procedures were followed.

Cases involving pharmaceuticals, medical devices, food safety, and cosmetics often require an FDA Approval expert witness. These experts are crucial in product liability or patent infringement cases.

In pharmaceutical litigation, an FDA Approval expert can provide testimony on drug development, clinical trials, labeling requirements, and post-market surveillance to establish if there was any negligence.

Yes, some experts specialize in specific areas like pharmaceuticals, medical devices, biologics, dietary supplements, or food products depending on their experience with FDA regulations.

Regulations and guidelines from the FDA frequently change. An expert with recent industry experience will have up-to-date knowledge about these changes and how they impact your case.

Expert Institute offers a personalized approach to help you find the highest quality experts. We source actively-practicing professionals who match all your requirements for specialty areas, work experience, litigation history, fee range, certifications, location, and more.

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