Discovery
Support for lead qualification and synthesis of new molecular entities (NMEs) and biologics.
BioPharma Services
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.
Services by phase
Eurofins Discovery is a global contact research organisation (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 skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Preclinical and Early Development
Services and support to assess safety of biopharma products, biological activity pharmacology services and toxicity and DMPK testing.
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 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.
BioAnalysis and Phase I Clinics is a global leader for bioanalysis, biomarker assay development, validation and sample analysis for both pre-clinical and clinical studies
Eurofins PSS Insourcing Solutions places skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Clinical Research and Development
Services and support to assess safety dosage and efficacy of biopharma products in Phase I,II and III studies.
High quality anatomical pathology services, delivering expert histopathology evaluation and reliable insights to support preclinical and clinical research.
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 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 & regulatory ready processes for complex clinical trials.
Approval
Services and support to verify safety, effectiveness, and controls.
High quality anatomical pathology services, delivering expert histopathology evaluation and reliable insights to support preclinical and clinical research.
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 skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Advanced laboratory expertise spans infectious disease, immunology, molecular testing, and cell & gene therapy, supported by global logistics & regulatory ready processes for complex clinical trials.
Commercial
Assessment of long-term effectiveness in Phase IV studies in addition to surveillance and quality control support.
High quality anatomical pathology services, delivering expert histopathology evaluation and reliable insights to support preclinical and clinical research.
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 skilled teams directly at client sites, with 20+ years of experience in mastering scientific operations and HR best practices.
Advanced laboratory expertise spans infectious disease, immunology, molecular testing, and cell & gene therapy, supported by global logistics & regulatory ready processes for complex clinical trials.
Find a site near you!
Select Business Line
Select Country
Clear Filters
Reset Filters
Getting the map ready...
