Eurofins CDMO is a leading global Contract Development and Manufacturing Organization (CDMO) that provides clients with Active Pharmaceutical Ingredients (APIs) / Drug Substance and Drug Product development for biologicals and small molecules. Science is our foundation 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.
Our service
Drug Substance/API development
Solid State Research & Development
Pre-Formulation, Formulation Development
Analytical Development
Sterile GMP Manufacturing
Non-Sterile GMP Manufacturing
Clinical packaging and logistics
Project management
CMC RA
We are experts in breakthrough technologies for APIs / Drug Substance and Drug Product development, highly potent compounds, poorly soluble drugs, lyophilization processes and specific therapeutic areas (immunotherapies, orphan drugs, pediatric dosage forms, etc.)
CDMO Services
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CDMO Services
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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
