Regulatory affairs expert witnesses draw on careers in pharma, biotech, medical devices, and healthcare products to clarify compliance with FDA, EMA, and other regulatory frameworks. They evaluate submissions, labeling, quality systems, post-market surveillance, and risk management, and assess whether regulatory strategies, documentation, and decisions met applicable standards.
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