API Development Services

Eurofins CDMO is an FDA-approved contract development and manufacturing organization (CDMO) focused on process chemistry, cGMP scale-up and analytical method development for complex, small molecule APIs, including highly potent molecules. Our talented team of Process Research, Analytical, Technology Transfer, CMC Specialists and Project Managers have supported clients from the pre-clinical phase through IND development, into late phase and commercial activities. Our work spans from route selection to process and analytical development, to non-cGMP and cGMP scale-up. Eurofins CDMO also supports criticality assessment and mitigation, CMC filing support, and supply chain management. We work closely with clients to provide phase-appropriate solutions to balance their immediate and long-term API development needs.