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
- 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
Company Details
- Employees
- 407
- Founded
- -
- Address
- 2 Bis Avenue De Gascogne, Fontenilles,haute-Garonne 31470,france
- Industry
- Pharmaceutical Manufacturing
- NAICS
-
Pharmaceutical and Medicine ManufacturingMedicinal and Botanical ManufacturingPharmaceutical Preparation ManufacturingIn-Vitro Diagnostic Substance ManufacturingBiological Product (except Diagnostic) Manufacturing
- Website
- http://www.eurofins.com/cdmo/
- Keywords
- analytical services, bioanalytical, quality control, in life studies, CDMO, formulation, small molecules, biologics, drug product, R&D, chemistry, microbiology, stability studies, testing, sterile manufacturing, method development, clinical packaging and logistics, USP/DSP, Fill & Finish, Life Cycle Management, API, cell banking, drug development.
- HQ
- Fontenilles, Haute-Garonne
Eurofins Cdmo Questions
Eurofins Cdmo's website is http://www.eurofins.com/cdmo/
Eurofins Cdmo's LinkedIn profile is https://fr.linkedin.com/company/eurofinscdmo
Eurofins Cdmo has
407 employees.
View email and phone details for 407
employees at Eurofins Cdmo.
Eurofins Cdmo's industry is
Pharmaceutical Manufacturing
Eurofins Cdmo's top competitors are
Sanofi,
Eurofins,
Eurofins Cdmo Alphora,
Eurofins Advinus,
Thermo Fisher Scientific,
Unither Pharmaceuticals,
Apotex Inc.,
Eurofins Genomics Americas,
Cdmo France,
Corden Pharma - A Full-Service Cdmo.
Eurofins Cdmo's categories are Pharmaceutical Manufacturing
Eurofins Cdmo's founding year is 2010
