Indiana FDA regulations expert witnesses help clarify FDA compliance across drug, device, and biologics development, manufacturing, and postmarket surveillance. They often come from regulatory affairs, quality systems, pharmacovigilance, and clinical research roles tied to Indiana University Health and the state’s life sciences corridor. They evaluate labeling, GMPs, adverse event reporting, and regulatory decision-making.
Medicaid Program Integrity Regulations Expert Witness
Medicaid Program Integrity Regulations Expert Witness
- Review Fee
- $500/hr
- Deposition Fee
- $500/hr
- Court Fee
- $700/hr
This highly qualified expert earned his BA in political science from Ohio State University. He then went on to serve as a mediator for consumer protection at the Office of the Indiana Attorney General. He also served as the Director of Medicaid contract management, the director of Provider Relations for Indiana Medicaid and as the Medicaid Program Integrity Director at Indiana Family and Social Services Administration. Currently, he is a senior advisor at a healthcare consultancy in Indiana.
Senior Advisor, A healthcare government affairs consultancy in IN
Bachelor of Arts (BA), Ohio State University
Zionsville,
Indiana