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 (Contract Development & Manufacturing Organization) helps pharmaceutical and biopharmaceutical companies move rapidly from research stage of their drug development to clinical stages with integrated services to compress timelines to market.
From formulation screening and development, analytical development, stability studies and pre-clinical safety assessment studies to sterile and non-sterile manufacturing, IND/ IMPD and NDA/ CTD services, as well as clinical trial material including packaging and logistics, Eurofins CDMO delivers comprehensive solutions to streamline the development and manufacturing of a variety of product types, delivery systems and dosage forms.
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