Eurofins CDMO empowers your biologics projects. Our state-of-the-art R&D laboratories and GMP-compliant cleanroom facilities enable us to support your projects from early-stage development to clinical supply and manufacturing
We are experts in innovative formulations that optimise stability and bioavailability. We offer solutions for proteins, antibodies, peptides, live biotherapeutic products, plasmid DNA and oligonucleotides. Eurofins CDMO partners with you to deliver preclinical to early-phase clinical and commercial formulations.
Formulation screening is performed during drug product development and administration. Different types of buffers and excipients are tested in order to stabilise the drug substance taking into account the needs for the applied delivery route. Information gathered during pre-formulation screening will speed up this process.
Various drug delivery routes are selected and compared to one another in terms of stability, efficacy and feasibility. Eurofins CDMO has experience with a wide range of different drug delivery routes, drug delivery systems and drug production technologies.