
Growth media optimisation
To maximise product yield, Eurofins CDMO provides titer optimisation for cell culture media
Eurofins CDMO offers a comprehensive suite of services to support your drug programmes, from early development, clinical to commercial
Leveraging advanced technology, Eurofins CDMO adeptly manages diverse batch sizes. With 200 L fed-batch and perfusion capabilities, Eurofins CDMO is dedicated to the development and scaling of monoclonal antibodies (mAbs).
As a global CDMO for biologics, we support the rapid advancement of mammalian and bioconjugate therapies through integrated development, conjugation, and manufacturing solutions. Leveraging deep scientific expertise and specialised technologies, we guide your molecule from laboratory to clinic and beyond.
To maximise product yield, Eurofins CDMO provides titer optimisation for cell culture media
With extensive capabilities for development, manufacturing and characterisation of cell banks, Eurofins CDMO offers cell banking services for research cell banks (RCBs)
Eurofins CDMO provides customised services according to client needs, and can efficiently store cell research cell banks (RCBs), Master Cell Banks (MCBs) and Working Cell Banks (WCBs)
Using Design of Experiments (DoE) approach, Eurofins CDMO integrates, single-use processing trains to develop processes that simplify manufacturing and reduce contamination risks with expertise in Risk Group 2 for exosomes, VLPs, EVLPs, ADCs, mAbs and recombinant proteins
Using our expertise in cell line characteristics, we design and optimise cell culture conditions (media, feeds, and process parameters) to drive superior cell growth, viability, and specific productivity of any target biologic. Our experts are experienced in developing and implementing both high-performing fed-batch processes for maximising volumetric productivity and advanced perfusion strategies for intensified, continuous manufacturing, enabling higher cell densities and increased product throughput.
Our DSP team has both width and depth in experience with purification of a wide range of proteins from a multitude of feedstocks. Furthermore, our team’s expertise in downstream processing ensures that we can successfully purify everything from monoclonal antibodies to more challenging or difficult to purify proteins.
Eurofins CDMO can support clinical manufacturing up to 200L scale. By April 2026 the production capacity will increase to 2000L scale with the addition of a new, full single use production train.
Analytical method development, GMP method validation, release and stability testing to support upstream and downstream process analytical testing, and services to support characterisation of drug product and life cycle management of analytical methods