FDA Regulations Expert Witnesses in Pennsylvania
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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 Pennsylvania
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Medical Device Regulations Expert Witness
This highly qualified expert has over 40 years of experience in medical device regulations. He received his BS in chemical engineering from Lowell Technological Institute and earned his MS in chemical engineering from the University of Iowa. He currently has 5 patents. Over the years, his work has included antimicrobial development and application, hydrophilic coating development and implementation, and over-the-counter and personal care product development. His former positions include research engineer for Eastman Kodak and GAF Corporation, project manager and laboratory supervisor for Biosearch Medical Products and Hydromer, and corporate manager of materials for Arrow International. Currently, this expert is the president of a medical device consulting company in Pennsylvania.
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President, A medical device consulting company in PA
Master of Science (MS), SUNY Binghamton
Blandon |
Pennsylvania
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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.