As an FDA registered 503B Outsourcing facility, Edge Pharma provides important services for pharmacists compounding drug products within their organization, as well as pharmaceutical companies planning a clinical drug trial.

Edge Pharma provides comprehensive training in compounding, focusing on USP 795, 797, 800, and 825 standards and Good Manufacturing Practice (GMP) guidelines.

Edge Pharma produces GMP material for clinical drug trials, including investigational product in complex dosages, concentrations, and schedules.

Call or send us a message to discuss your needs in our services. A member of our team will reach out to you shortly.