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Services by phase

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Discovery

Lead qualification
Synthesise NME or new biologic

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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.

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Preclinical and Early Development

Assess safety and biological activity pharmacology, toxicity & DMPK

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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.

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Clinical Research and Development

Assess safety, dosage and efficacy in humans
Phase I, II, and III studies

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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.

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Approval

Verify safety, effectiveness and controls to agency

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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.

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Commercial

Assess long-term effectiveness (Phase IV studies)
Surveillance/Quality control

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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.

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Media Center

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Monday, 10/03/2025

GMP next generation sequencing optimally delivers rapid, cost-effective results to assure product safety News

Identity tests are a crucial part of product testing packages submitted to regulatory agencies during the drug development and approval lifecycle

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