Wisconsin FDA regulations expert witnesses help interpret FDA requirements for drugs, devices, and biologics across development, labeling, and postmarket compliance. They often come from regulatory affairs, quality systems, pharmacovigilance, and clinical research roles within Madison’s biotech corridor and major health systems. These experts commonly evaluate GMP adherence, adverse event reporting, promotional claims, and regulatory decision-making.
FDA Regulatory Policy and Congressional Oversight Expert Witness
FDA Regulatory Policy and Congressional Oversight Expert Witness
- Review Fee
- $500/hr
- Deposition Fee
- $500/hr
- Court Fee
- $500/hr
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.
President, A Biotech Consultancy
Master of Science (MS), University of Texas at Austin
Milwaukee,
Wisconsin