FDA Regulations Expert Witnesses in Wisconsin
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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 Wisconsin
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FDA Regulations Congressional oversight Expert Witness
This expert is the president of a healthcare government relations and regulatory policy consultancy firm that she founded after an extensive career in healthcare and government. She was the Vice President for Government Relations and Public Policy at Celgene and was the Vice President for Regulatory Policy at GE Healthcare. She served in the administration of President George H.W. Bush as Special Assistant for Legislative and Public Affairs in the Office of the Commissioner, US Food and Drug Administration. She is a certified Regulatory Affairs specialist and is the author of numerous reports and is currently on the Board of Directors of the FDA Alumni Association. Her formal education includes a BA in Government from Georgetown University and an MS in Science and Technology Commercialization from The University of Texas at Austin.
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President, A Biotech Consultancy
Master of Science (MS), University of Texas at Austin
Milwaukee |
Wisconsin
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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.