Discovery
Lead qualification
Synthesise NME or new biologic
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 CRO offering over 23,000 products and services to drug discovery researchers developed in 40+ years of industry leadership.
Eurofins Genomics specializes 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.
Preclinical and Early Development
Assess safety and biological activity pharmacology, toxicity & DMPK
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 specializes in drug development and manufacturing for biologics and small molecules, ensuring comprehensive support throughout the drug development process.
Eurofins Genomics specializes 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.
Clinical Research and Development
Assess safety, dosage and efficacy in humans
Phase I, II, and III studies
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 specializes in drug development and manufacturing for biologics and small molecules, ensuring comprehensive support throughout the drug development process.
Eurofins Genomics specializes 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.
Approval
Verify safety, effectiveness and controls to agency
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 specializes in drug development and manufacturing for biologics and small molecules, ensuring comprehensive support throughout the drug development process.
Eurofins Genomics specializes 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.
Commercial
Assess long-term effectiveness (Phase IV studies)
Surveillance/Quality control
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 specializes 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 specializes 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.
