Description
Eurofins CDMO Europe is a prominent supplier to the pharmaceutical industry, offering a wide range of services in the fields of Active Pharmaceutical Ingredients (APIs), Contract Manufacturing (CMO/CDMO), and Clinical Research Organisations (CRO). Specialising in both biologics and small molecules, Eurofins CDMO provides comprehensive solutions for drug substance manufacturing, drug product formulation, and clinical trial materials. Their extensive network includes state-of-the-art facilities across Europe, ensuring adherence to good manufacturing practices (GMP) and providing high-quality support throughout the entire drug development lifecycle.
Services include:
- Small Molecule
- Biologics
- Cell and Gene Therapy
- Drug Substance Manufacturing (API)
- Drug Product Formulation (FDF)
- Research & Development
- Clinical Trial Materials
- Packaging
- Regulatory Services
- Analytical Methods Development
- Analytical Services
- Bioprocess Validation
- Cell Culture Media Development
- cGMP Synthesis
- Contaminant Analysis
- Contract Research (CRO)
- Custom Synthesis
- Dissolution Testing
- Drug Development
- Efficacy Testing
- Endotoxin Testing & Removal
- Environmental Monitoring
- Testing
- Feasibility Studies
- Forced Degradation Studies
- Process Development
- Formulation Development
- Controlled Release
- Gene Therapy & Testing Protocols
- Immunotoxicity Testing
- In Vitro Testing
- Lot Release Testing
- Lyophilization
- Mammalian Cell Culture
- Micro FT-IR Analysis
- Microbiological Testing
- Mycoplasma Testing
- Particle Characterization
- Particle Size Analysis
- Particle Size Classification
- Preformulation
- Quality QA/QC
- Radiopharmaceuticals
- Raw Materials Analysis
- Stability Studies
- Stability
- ICH
- Sterile Filling
- Sterility Testing
- Thermogravimetric Analysis
- Trace Metal Analysis
- ICP
- UV-VIS Spectrophotometer Analysis
- Virology
- X-Ray Powder Diffraction
- Aseptic Fill/Finish
- Chemistry (CMC)
- Manufacturing
- Contract Development and Manufacturing (CDMO)
- Dosage Form Development
- Filling
- Syringe
- Vials
- Aseptic Fill-Finish
- Semisolids
- Clinical Trials
- Parenterals
- Accelerated Stability Studies
- Assay Development
- Chromatography
- Contract Manufacturing (CMO)
- APIs (Active Pharmaceutical Ingredients)
- Bioanalytical Services
- Biological Testing
- Biomarker Research
- Biosimilars
- Lab Services
- Contract Packaging
- Ampule
- Capsule
- Cartridge
- Genomics and Screening
- Immunobiology Services
- Informatics
- Supply Chain & Logistics
- Mass Spectrometry
- Nonclinical Research
- Banding
- Blister
- Cold Form
- Closures
- Compliance
- Machinery & Equipment
- Asceptic Fill-Finish
- Glass
- Injectables
- Labelling
- Liquids
- Lotion Pumps
- Plastic Bottles and Jars
- Pouches
- Powders
- RFID
- Samples
- Solid Dosage
- Spray Pumps
- Tubes
- Unit Dosage
- Pharmacodynamics
- Pharmacogenomics
- Pharmacokinetics
- Polymerase Chain Reaction
- Preclinical Testing
- Process Validation Studies
- Storage
- Technology Transfer
- Logistics
- Torque Testing
- Translation Services
- Validation
- Clinical
- Warehousing
Eurofins CDMO Europe is dedicated to advancing pharmaceutical development through their extensive array of services tailored to meet the needs of the industry.
Capabilities
- Accelerated Stability Studies
- Ampule
- Analytical Methods Development
- Analytical Services
- APIs (Active Pharmaceutical Ingredients)
- Asceptic Fill-Finish
- Assay Development
- Banding
- Bioanalytical Services
- Biological Testing
- Biologics
- Biomarker Research
- Bioprocess Validation
- Biosimilars
- Blister
- Capsule
- Cartridge
- Cell and Gene Therapy
- Cell Culture Media Development
- cGMP Synthesis
- Chemistry (CMC)
- Chromatography
- Clinical
- Clinical Trial Materials
- Clinical Trials
- Closures
- Cold Form
- Compliance
- Contaminant Analysis
- Contract Development and Manufacturing (CDMO)
- Contract Packaging
- Contract Research (CRO)
- Controlled Release
- Custom Synthesis
- Dissolution Testing
- Dosage Form Development
- Drug Development
- Drug Product Formulation (FDF)
- Drug Substance Manufacturing (API)
- Endotoxin Testing & Removal
- Environmental Monitoring
- Feasibility Studies
- Filling
- Forced Degradation Studies
- Formulation Development
- Genomics and Screening
- Glass
- ICH
- ICP
- Immunobiology Services
- Immunotoxicity Testing
- In Vitro Testing
- Informatics
- Injectables
- Lab Services
- Labelling
- Liquids
- Lot Release Testing
- Lotion Pumps
- Lyophilization
- Machinery & Equipment
- Mammalian Cell Culture
- Mass Spectrometry
- Micro FT-IR Analysis
- Microbiological Testing
- Mycoplasma Testing
- Nonclinical Research
- Packaging
- Parenterals
- Particle Size Analysis
- Pharmacodynamics
- Pharmacogenomics
- Pharmacokinetics
- Plastic Bottles and Jars
- Polymerase Chain Reaction
- Pouches
- Powders
- Preclinical Testing
- Preformulation
- Process Development
- Process Validation Studies
- Quality QA/QC
- Radiopharmaceuticals
- Raw Materials Analysis
- Regulatory Services
- Research & Development
- RFID
- Samples
- Semisolids
- Small Molecule
- Solid Dosage
- Spray Pumps
- Stability Studies
- Sterile Filling
- Sterility Testing
- Storage
- Supply Chain & Logistics
- Syringe
- Technology Transfer
- Testing
- Thermogravimetric Analysis
- Torque Testing
- Trace Metal Analysis
- Translation Services
- Tubes
- Unit Dosage
- UV-VIS Spectrophotometer Analysis
- Validation
- Vials
- Virology
- Warehousing
- X-Ray Powder Diffraction
Contact Information
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