Idaho FDA regulations expert witnesses assess compliance for drugs, devices, and biologics across clinical and manufacturing settings. They often come from regulatory affairs, pharmacy, quality systems, and clinician leadership at Boise-based health systems and regional medical device and food producers. They evaluate labeling, adverse event reporting, GMPs, and FDA enforcement risk.
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