Partnering to Expedite Your Product’s Success
Discovery
Your End-to-End Provider
From discovery to lead selection to process optimization to cGMP manufacturing, our U.S. facilities ensure your biological programs will reach the targets of your non-clinical and clinical program.
Development
From Validation to Sterile Fill-Finish
Curia gives you an inside track with stable mammalian cell line development, upstream/downstream process development, and the ability to provide end-to-end development of sterile fill-finish products in various formats including vials, pre-filled syringes, and cartridges.
Manufacturing
Rely on Our Expertise
Curia’s U.S. facilities provide cGMP manufacturing services to take your program from IND to commercial-ready. Our approach has been to appropriately provide the scales and services to reach your goal with a conscientious and efficient approach. Our team provides a vast array of experience and diagnostic tactics to engage programs and communicate all activities with meticulousness detail.
Ready to realize your product’s full potential on your schedule?