Our services

Expert GMP manufacturing and development of complex biologics, driven by skilled professionals delivering robust solutions from cell banking to clinical supply.

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Buffer preparation

As part of end-to-end projects or as stand-alone activity, from small buffer volumes to productions up to 2000 L batches.

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  • 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)
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USP/DSP manufacturing activities

Eurofins CDMO delivers GMP manufacturing capabilities up to 2000 L scale, with:

-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

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GMP biologics drug substance cleanrooms

-Human IMP licensed manufacturing facility (FAHMP)
Grade C suites, ISO 5/7 cleanrooms

-Biosafety level 2 classified rooms

-Cutting-edge technologies and methodologies to enhance the efficiency and reliability of manufacturing processes

-Environmental monitoring program