Eurofins Amatsigroup becomes Eurofins CDMO

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Eurofins Amatsigroup becomes Eurofins CDMO

Eurofins CDMO - Contract Development Manufacturing Organization - provides integrated, end to end solutions for preclinical & clinical outsourcing services of both Drug Substance/API and Drug Product for biologicals and small molecules.

Eurofins CDMO is your drug development partner:

Support our clients to move rapidly through the drug development value chain
Perform complex formulation screening and development until sterile and non sterile manufacturing
Accelerate process development and scale-up under GMP or non-GMP compliance
Provide clinical trial material including packaging and logistics
Ensure regulatory compliance throughout each stage of the development cycle with a full CMC-Ra support

We help pharmaceutical and biopharmaceutical companies to move rapidly from research stage of their drug development to clinical steps with integrated services to compress timelines to market.

With more than 30 years of experience in preclinical and clinical development, our expert teams ensure your clinical trials achievements.

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