Alabama FDA regulations expert witnesses clarify how FDA rules apply to drugs, devices, and clinical research in local care settings. Many are regulatory affairs leaders, quality and compliance officers, pharmacists, and physicians tied to UAB Medicine and Alabama’s medical device manufacturing corridor. They evaluate labeling, adverse event reporting, GMP compliance, and investigational protocol adherence.
Pharmaceutical Quality & FDA Regulatory Compliance Expert Witness
Pharmaceutical Quality & FDA Regulatory Compliance Expert Witness
- Review Fee
- $250/hr
- Deposition Fee
- $500/hr
- Court Fee
- $500/hr
This expert has over 40 years of experience in the Pharmaceutical and Pharmaceutical Packaging industries. He has published five books and has instructed professionals at the graduate level in Quality Assurance and Regulatory Affairs at a major university's pharmacy school. As a former Director of the Science Branch of the Philadelphia District FDA, he directed a laboratory staff of 30 in methods verification of New Drug Applications and Abbreviated New Drug Applications, Drug Product Surveys, and Research Projects. Currently, this expert is an independent consultant in which he assists pharmaceutical firms in technical, regulatory, and management areas to ensure their clients' products hit the market in a timely manner. He assists attorneys as an Expert Witness/Subject Matter Expert in Pharmaceutical cases.
Founder/Principal, A consulting services for pharmaceutical firms
Master of Business Administration (MBA), Temple University
Savannah,
Georgia