Nevada FDA regulations expert witnesses help interpret federal compliance requirements for drugs, devices, and biologics used across Las Vegas and Reno healthcare systems. They often come from regulatory affairs, quality assurance, clinical research, and pharmacy leadership roles tied to Nevada’s growing life sciences and medical device activity. They evaluate labeling, adverse event reporting, GMP controls, and FDA correspondence.
Nutrition Regulatory Affairs & Product Labeling Expert Witness
Nutrition Regulatory Affairs & Product Labeling Expert Witness
- Review Fee
- $250/hr
- Deposition Fee
- $310/hr
- Court Fee
- $310/hr
This Nutrition industry professional has an advanced degree in nutrition, and several years of experience involving the technical aspects of regulatory affairs, scientific affairs, product labeling, and research & development. His specialties: 21 CFR 101 (Food Labeling), 21 CFR 111 (cGMPs for dietary supplements), FTC advertising guidelines, regulatory compliance review, product substantiation, ingredient research and product development. In his current role as Manager at a Vitamin research company he is responsible for reviewing products, labeling and marketing materials for FDA and FTC compliance.
VP, A dietary supplement company in ID
Master of Science (MS), University of Saint Joseph
Eagle,
Nevada