Year of expertise
GMP biologics manufacturing process
We accompany our partners from the first contact to their drug substance release.
A dedicated project manager is assigned to each contract to communicate with our
partners throughout the whole manufacturing process.
GMP grade quality
- GMP accredited since 1994
- US FDA inspected CDMO
- >50 Big Pharma audits
Experience in microbial fermentation since 1994
At Eurogentec we are experts in microbial fermentation and purification of high titers GMP biologics at large scales.
We manufacture biopharmaceuticals from bacteria and yeast according to FDA, EMA and PMDA requirements.
We produce biologics in all major microbial strains: E. coli, P. pastoris, H. polymorpha, S. cerevisiae
and biosafety level 2 micro-organisms that are non-sporulating.