Our companies work with pharmaceutical, chemical, biotechnology, medical device and cosmetic clients to cover the whole chain of drug development, thanks to an international network of laboratories and testing units with global reach, uniform QA systems, and high-quality services.
- Lead qualification
- Synthesise NME or new biologics
Eurofins Discovery is a global CRO offering over 23,000 products and services to drug discovery researchers developed in 40+ years of industry leadership.
Eurofins Genomics specialises in creating synthetic DNA/RNA called oligonucleotides and genes, and sequencing services including Nanopore plasmid sequencing, Sanger sequencing, and NGS sequencing.
Eurofins Medical Device Services offers regulatory compliance expertise and GMP/GLP/ISO 17025 testing to ensure rapid turnaround times with the highest level of service and advanced technologies.
Eurofins PSS Insourcing Solutions places our skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Assess safety and biological activity pharmacology, toxicity and DMPK
Eurofins Bioanalytical Services offers 20+ years of scientific expertise in PK/TK, ADA, NAb and biomarker assay development, validation and sample analysis for both pre-clinical and clinical studies.
Eurofins BioPharma Product Testing is a GMP laboratory supporting ADCs, biotherapeutics, cell & gene therapies, mAbs, mRNA/NATs, oncolytic viruses, peptides, small molecule, and therapeutic proteins.
Eurofins CDMO specialises in drug development and manufacturing for biologics and small molecules, ensuring comprehensive support throughout the drug development process.
Eurofins Genomics specialises in creating synthetic DNA/RNA called oligonucleotides and genes, and sequencing services including Nanopore plasmid sequencing, Sanger sequencing, and NGS sequencing.
Eurofins Medical Device Services offers regulatory compliance expertise and GMP/GLP/ISO 17025 testing to ensure rapid turnaround times with the highest level of service and advanced technologies.
Comprehensive scientific capabilities support seamless progression from pre clinical studies into early development with reliable, high quality data.
Eurofins PSS Insourcing Solutions places our skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
- Assess safety, dosage and efficacy in humans
- Phase I, II, and III studies
Eurofins Central Laboratory is a leading provider of clinical trial pathology services, leveraging more than 30 years of experience and deep scientific expertise to help sponsors maximise insights.
Eurofins Bioanalytical Services offers 20+ years of scientific expertise in PK/TK, ADA, NAb & biomarker assay development, validation and sample analysis for both pre-clinical and clinical studies.
Eurofins BioPharma Product Testing is a GMP laboratory supporting ADCs, biotherapeutics, cell & gene therapies, mAbs, mRNA/NATs, oncolytic viruses, peptides, small molecule, and therapeutic proteins.
Eurofins Central Laboratory offers safety, efficacy, biomarker, and pathology services, through our global network of CAP accredited laboratories supporting clinical trials in over 85 countries.
Eurofins CDMO specialises in drug development and manufacturing for biologics and small molecules, ensuring comprehensive support throughout the drug development process.
Scientifically rigorous bioanalytical and biomarker capabilities support early phase studies, generating reliable data from first in human through early clinical development.
Eurofins Genomics specialises in creating synthetic DNA/RNA called oligonucleotides and genes, and sequencing services including Nanopore plasmid sequencing, Sanger sequencing, and NGS sequencing.
Eurofins Medical Device Services offers regulatory compliance expertise and GMP/GLP/ISO 17025 testing to ensure rapid turnaround times with the highest level of service and advanced technologies.
Comprehensive scientific capabilities support seamless progression from pre clinical studies into early development with reliable, high quality data.
Eurofins PSS Insourcing Solutions places our skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Advanced scientific expertise spans infectious disease, immunology, molecular testing and cell & gene therapy, supported by global logistics and regulatory ready processes for complex clinical trials.
Verify safety, effectiveness and controls to agency
Eurofins Central Laboratory is a leading provider of clinical trial pathology services, leveraging more than 30 years of experience and deep scientific expertise to help sponsors maximise insights.
Eurofins BioPharma Product Testing is a GMP laboratory supporting ADCs, biotherapeutics, cell & gene therapies, mAbs, mRNA/NATs, oncolytic viruses, peptides, small molecule, and therapeutic proteins.
Eurofins Central Laboratory offers safety, efficacy, biomarker, and pathology services, through our global network of CAP accredited laboratories supporting clinical trials in over 85 countries.
Eurofins CDMO specialises in drug development and manufacturing for biologics and small molecules, ensuring comprehensive support throughout the drug development process.
Eurofins Genomics specialises in creating synthetic DNA/RNA called oligonucleotides and genes, and sequencing services including Nanopore plasmid sequencing, Sanger sequencing, and NGS sequencing.
Eurofins Medical Device Services offers regulatory compliance expertise and GMP/GLP/ISO 17025 testing to ensure rapid turnaround times with the highest level of service and advanced technologies.
Eurofins PSS Insourcing Solutions places our skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Advanced scientific expertise spans infectious disease, immunology, molecular testing and cell & gene therapy, supported by global logistics and regulatory ready processes for complex clinical trials.
- Assess long-term effectiveness (Phase IV studies)
- Surveillance/Quality control
Eurofins Central Laboratory is a leading provider of clinical trial pathology services, leveraging more than 30 years of experience and deep scientific expertise to help sponsors maximise insights.
Eurofins BioPharma Product Testing is a GMP laboratory supporting ADCs, biotherapeutics, cell & gene therapies, mAbs, mRNA/NATs, oncolytic viruses, peptides, small molecule, and therapeutic proteins.
Eurofins CDMO specialises in drug development and manufacturing for biologics and small molecules, ensuring comprehensive support throughout the drug development process.
Eurofins Central Laboratory offers safety, efficacy, biomarker, and pathology services, through our global network of CAP accredited laboratories supporting clinical trials in over 85 countries.
Eurofins Genomics specialises in creating synthetic DNA/RNA called oligonucleotides and genes, and sequencing services including Nanopore plasmid sequencing, Sanger sequencing, and NGS sequencing.
Eurofins Medical Device Services offers regulatory compliance expertise and GMP/GLP/ISO 17025 testing to ensure rapid turnaround times with the highest level of service and advanced technologies.
Eurofins PSS Insourcing Solutions places our skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Advanced scientific expertise spans infectious disease, immunology, molecular testing and cell & gene therapy, supported by global logistics and regulatory ready processes for complex clinical trials.