Xcelience is a premier provider of formulation development and manufacturing solutions with a solid reputation for accelerating early phase small molecule development. Our outstanding quality record, significant drug development expertise, willingness to customize, and disciplined project management enable us to deliver real advantage to clients with the need to speed potential drugs to clinical trials.
Since 1997, Xcelience has been renowned for reliably expediting drug product development for oral solid, semi-solid and liquid dosage forms. Our formulation development scientists have considerable experience overcoming challenging associated with physical and chemical properties of drug substance, or limited quantities of active pharmaceutical ingredient (API), in a manner that results in compounds with improved solubility and bioavailability. Xcelience operates out of a cGMP compliant, FDA audited, DEA licensed facility in Tampa, Florida.
Xcelience is more than just the market leader for powder-in-capsule services, which enable clients to fill very small amounts of API into capsule and reduce time to first-in-human studies by as much as 45% relative to traditional drug development programs, we are a full spectrum formulation development and manufacturing provider. Our recently expanded process technology capabilities reflect our continued commitment to help clients build towards improved manufacturing outcomes in a manner consistent with the FDA’s Quality by Design initiative.
Regions where services are provided:
North America and Europe
Outsourcing serivces provided:
Development and Phase I/IICTM
Packaging and Logistics
Partnering with a specialist like Xcelience for early phase development can reduce product risk and accelerate drug development timelines. For more information, contact Xcelience at 608.643.4444 or visit www.xcelience.com.