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

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Discovery

Support regarding lead qualification and new biologics.

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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 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.

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Preclinical and Early Development

Services and support to assess safety of biopharma products, biological activity pharmacology services and toxicity and DMPK testing.

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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 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.

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Clinical Research and Development

Services and support to assess safety dosage and efficacy of biopharma products in Phase I,II and III studies.

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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 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.

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Approval

Services and support to verify safety, effectiveness, and controls.

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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 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.

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Commercial

Assessment of long-term effectiveness in Phase IV studies, and surveillance and quality control support.

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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 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.

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