Custom Development

If you’re looking to outsource drug product development to a CDMO, you need a collaborative partner who will commit to understanding the unique needs of your project. Cambrex offers broad drug product development capabilities and the manufacturing infrastructure to bring your molecule seamlessly through clinical development and commercialization.

In fulfilling all aspects of the CMC dosage form section of the NDA, our laboratories, pilot facilities, and scientists are with you at every stage of the pharmaceutical development process. We can take your products through excipient iterations, pre-formulation and formulation activities and advance them through to the manufacture of clinical trial materials to exacting standards.

Our integrated analytical services provide the method development and validation support you need for your registration package — flexibly, efficiently and with an excellent EMEA, HPFBI, EMA and FDA inspection record.