Pharmaceutical Contract Manufacturing Services

One purpose-built facility covers proof of concept, Phase I-IV clinical supply, commercial manufacturing and packaging, with continuous monitoring of temperature, humidity and pressure and real-time notification.

Potent compounds are handled in segregated Grade C and D clean room suites with dedicated air handling. Blinding options for study materials include over-encapsulation, logo removal and confusion-print over-printing. APIs can be wet milled to nano size, and Grade C injectable suites, inspected by both FDA and European Union Quality Personnel, support sterilization by heat, gamma or e-beam. The site holds DEA licenses for Schedules I through V, with vaults for Schedules I-II.

Explore the full service profile for the complete scope and registrations.