FDA Regulations Expert Witnesses in Rhode Island
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Average FDA Regulations Expert Witnesses Court Fees
$450/hr
Review Fee
$525/hr
Deposition Fee
$550/hr
Court Fee
FDA Regulations Experts in Rhode Island
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Chemistry & Pharmaceuticals Expert Witness
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 formulation, stability studies and the management of CROs. He earned his BA in chemistry from Rhode Island College before earning his PhD in chemistry from Brown University. He formerly served as a scientist at Eikos Inc and as the principal scientist and project coordinator at Paratek Pharmaceuticals. He then worked as a consultant in pharmaceutical development for H-3 Biomedicine and Cemotics. Currently, this expert is a professor of chemistry at a college and a pharmaceutical advisor at a consultancy in Rhode Island.
Consultant, A Pharmaceutical Consultancy in RI
Doctor of Philosophy (PhD), Brown University
Providence,
Rhode Island
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FAQs for Fda Regulations Expert Witnesses
What is the role of an FDA Regulations expert witness in a legal case?
An FDA Regulations expert witness provides insight on compliance, regulatory standards, and industry practices. They can testify on violations, product safety, and approval processes.
What types of cases might require an FDA Regulations expert witness?
Cases involving pharmaceuticals, medical devices, food safety, dietary supplements, cosmetics, or any product regulated by the FDA may require such an expert witness.
Can an FDA Regulations expert witness help with cases related to drug approval processes?
Yes. These experts can provide valuable insights into the complex process of drug approval and how deviations from this process can lead to legal issues.
Are there subspecialties within the field of FDA Regulations for expert witnesses?
Yes. Subspecialties can include pharmaceutical regulations, food safety standards, medical device regulations, cosmetic regulations, and more.
How can an FDA Regulations expert witness assist in a case involving adverse drug reactions?
They can evaluate whether the manufacturer complied with FDA regulations regarding reporting adverse events and if failure to comply contributed to harm.
How does Expert Institute select its FDA Regulations expert witnesses?
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.