Buffer preparation
As part of end-to-end projects or as stand-alone activity, from small buffer volumes to productions up to 200L/batch
cGMP Manufacturing
Our services
Expert GMP manufacturing and development of complex biologics, driven by skilled professionals delivering robust solutions from cell banking to clinical supply.
- Dedicated suites for buffer preparation
- Rapid turnaround to meet tight timelines
- Custom formulations
- In-house QC testing (pH, conductivity, osmolality, endotoxin testing, bioburden testing, visual inspection)
USP/DSP manufacturing activities
Eurofins CDMO delivers GMP clinical manufacturing capabilities up to 200L scale, with planned expansion to 2000L capacity through a new full single-use production train by April 2026.
Expertise in mAb manufacturing for bioconjugation, R&D, GLP toxicology, clinical supply (Phase I/II), and commercial production
Strategic partnerships with leading Cell Line Development vendors for high-titer, high-productivity cell lines
GMP biologics drug substance cleanrooms
Human IMP licensed manufacturing facility (FAHMP)
Grade C suites, ISO 5/7 cleanrooms
Cutting-edge technologies and methodologies to enhance the efficiency and reliability of manufacturing processes
Environmental monitoring programme
