Eurofins CDMO is a leading global Contract Development and Manufacturing Organization (CDMO) that provides clients with APIs / Drug Substance and Drug Product development for biologicals and small molecules. Science is our fondation and allows us to support small and major biopharmaceutical companies. Our sustainable and flexible methods help them achieve their pre-clinical and clinical milestones on time.
We are experts in breakthrough technologies for API development, highly potent compounds, poorly soluble drugs, lyophilisation processes and specific therapeutic areas (immunotherapies, orphan drugs, pediatric dosage forms, etc.)
Involved in the earliest steps, our highly-qualified project management team will propose a complete drug development strategy in compliance with regulations. Frequent communication through one single point of contact, our team’s flexibility, troubleshooting mindset, customized solutions will help speed up the drug development process. Operating under strict quality procedures, Eurofins CDMO is accredited through the FDA, EMA, ANSM, ANSES, FAMHP, PMDA, and Health Canada.
Our goal is to build a sustainable partnership with our customers to support their drug development pathway.
Our service offerings include:
- Drug Substance/API development
- Solid State Research & Development
- Pre-Formulation, Formulation Development
- Analytical Development
- Non-GMP & GMP Manufacturing
- Clinical packaging and logistics
- Project management
- CMC RA
Choose Eurofins CDMO to help you:
- Move rapidly through the drug development value chain (API/DS and DP)
- Perform complex formulation screening and development
- Accelerate process development and scale-up under GMP compliance
- Achieve clinical & small commercial manufacturing batches (Sterile and Non Sterile)
- Provide clinical trial material including packaging and logistics
- Ensure regulatory compliance throughout each stage of the development cycle with full CMC-RA support