We partner customers to accelerate their R&D pipeline through the development of robust and compliant drug products, achieving quality attributes and performance metrics for the successful completion of clinical studies. Extensive experience in NCE formulation development, combined with flexible strategies to meet customer needs, enable us to efficiently and rapidly resolve key challenges of dissolution, flowability, wettability, stability and bioavailability. With strong analytical skills in method development and validation, and a quality by design (QbD) approach, we facilitate speedy IND/NDA filing.
Our technology transfer team has successfully translated formulation technologies developed in our laboratories to manufacturing scale, to ensure timely supply of drug products for clinical trials.
Preformulation Studies
Formulation Development
Experience in developing technologies to support efficacy, PK and toxicology studies in different species.
A comprehensive range of solutions to develop and supply formulations for toxicology studies.
Reliable and reproducible analytical data to support speedy filing for regulatory approval.
