Eurofins CDMO (Contract Development Manufacturing Organization) can manage highly potent/cytotoxics projects.
Your specialty might be live APIs or even special type of biological entities that needs to be handled in a specific and GMP environment for the formulation and the development of all required services. This has been designed and implemented in multiple facilities of Eurofins CDMO. We are ready to help you in designing and developing your new Biological Safety Level 2 and 3 (upon facility upgrade) drug products in our laboratories.
Choose Eurofins CDMO to help you:
✔ Access to dedicated processes and equipments
✔ Get expertise from dedicated teams and development structures
✔ Perform sterile clinical & small commercial batches in dedicated suites and facilities
✔ Manage full aseptic formulation and development in non GMP and GMP environment for the success of your project