A robust development program is the future of any life science company. Getting a product from concept to market is already an expensive and time consuming undertaking. Don’t allow avoidable regulatory hurdles to slow the process even further. Saltbox Consulting can help. We offer Good Laboratory Practices advice; Good Clinical Practices advice; NDA, 510(k), and PMA application review, device classification and registration, cosmetic registration, and food additive applications. We can help respond to Complete Response Letters, requests for additional information, GCP and GLP investigations, and other FDA actions regarding potential new products.