Made for Pharma and BioTech companies

Are you looking for a reliable genomics partner?

Our genomics solutions support you along your drug development chain of small and large molecules, and in precision medicine

Eurofins pharma solutions

Solutions you need

Get best in class service and support for your project. Our experts would love to discuss the details of your project with you.

Eurofins pharma technologies

Essential technologies

We offer the latest technology and tools in many business areas. We support you in every stage of your process.

Eurofins pharma accreditations

Accreditations you expect

We know that complying with your requirements is a must, so all our labs are certified. Quality and reliability means everything to us.

Eurofins pharma solutions

Solutions you need

Get best in class service and support for your project. Our experts would love to discuss the details of your project with you.

Eurofins pharma technologies

Essential technologies

We offer the latest technology and tools in many business areas. We support you in every stage of your process.

Eurofins pharma accreditations

Accreditations you expect

We know that complying with your requirements is a must, so all our labs are certified. Quality and reliability means everything to us.

Does this sound familiar to you?

Your challenges

  • Complex project set-up
  • Many different stakeholders
  • High requirements for accreditations
  • Too many different service providers that only cover one aspect of the project
  • Often changing contact persons

We have long-standing expertise, a wide network of laboratories, and a product portfolio that supports your entire value chain.

Our GENOMICS Solutions for PHARMA / BIOTECH

We are the one provider that covers all aspects of your project

Along the entire value chain

Discovery

Discovery

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Genomic services for entire range of research questions: oligonucleotide production (primers, probes, NGS oligos), Sanger sequencing, gene synthesis, NGS, qPCR and microarray analysis.

Broad range of services, e.g., biomarker discovery and validation using NGS and microarrays or screening of antibody libraries.

Structural Variants

Pre-clinical development

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Manufacturing of small batches of therapeutic oligos or templates for mRNA production, toxicogenomic analysis.
Variants

Clinical trials

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For all drug classes: Patient screening regarding genetic conditions (Exome/panel sequencing/ HWGS, microarray analysis) and pharmacogenomics (qPCR, microarray) and molecular monitoring of drug effect on gene expression levels (RNASeq and qPCR).

For novel therapies:
Manufacturing of templates (synthetic genes) and primers for mRNA production.
QC for: mRNA templates, engineered cells in cell therapy (on-/off-target check), vectors and inserts.

Coming soon: Synthesis of siRNAs, ASOs and other RNA therapeutics.

Commercial phase

Commercial phase

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Coming soon:
Manufacturing of templates (synthetic genes) and primers for mRNA production. Synthesis of siRNAs, ASOs and other RNA therapeutics.

QC for: mRNA templates, treated cells in cell therapy (on-/off-target check), vectors and inserts.

Covering the entire range of drug classes

Small molecules

Small molecules

Antibodies and other protein therapeutics

RNA therapeutics

RNA therapeutics

Cell and gene therapy

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Impact on gene expression levels. Pharmacogenomics and toxicogenomics.

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Production of protein coding synthetic gene, sequence screening and confirmation of produced constructs, antibody purification.

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Manufacturing of templates (synthetic genes) and primers for mRNA production. Quality control for mRNA templates.

Coming soon: Synthesis of siRNAs, ASOs and other RNA therapeutics.

Read more

Patient screening for individualized therapy, quality control for engineered cells (confirmation of on-target, check for off-target effects), quality control for vectors and inserts.
Small molecules

Small molecules

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Impact on gene expression levels. Pharmacogenomics and toxicogenomics.

Antibodies and other protein therapeutics

Read more

Production of protein coding synthetic gene, sequence screening and confirmation of produced constructs, antibody purification.
RNA therapeutics

RNA therapeutics

Read more

Manufacturing of templates (synthetic genes) and primers for mRNA production. Quality control for mRNA templates.

Coming soon: Synthesis of siRNAs, ASOs and other RNA therapeutics.

Cell and gene therapy

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Patient screening for individualized therapy, quality control for engineered cells (confirmation of on-target, check for off-target effects), quality control for vectors and inserts.

Providing solutions for „hot topics“

Biomarkers

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Biomarker discovery and validation, monitoring during clinical trials. Broad spectrum of technologies with NGS, microarrays and qPCR.

Micobiome

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Microbiome characterization and monitoring of various sources like stool or skin swabs using NGS sequencing (16S amplicon or metagenome approach).

Pharmacogenomics

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Analysis of genetic precondition for metabolizing different active substances – individual pathways using Sanger sequencing or qPCR, holistic screening using microarray.
Biobanking

Toxicogenomics

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Effect of drugs on activation of different cellular pathways. Changes in gene expression are measured using RNASeq or microarray analysis.
We are the one provider that covers all aspects of your project

Benefit from our large network of labs and technologies

Eurofins Genomics, as part of Eurofins Scientific, is a market leader in testing and laboratory services for genomics, discovery pharmacology and clinical studies.

We support from research to application:

Pharma   |   Diagnostics   |   Biotechnology

With our globally unrivalled lab network, we support standard and challenging research projects, as well as complex strategies for large interdisciplinary companies.

Full scalability

100%

From one to thousands of samples.
Don’t be afraid to think big!

tackle your challenges

Our technologies

We provide everything you need:

  • Next-generation sequencing (NGS, Illumina)
  • Microarrays (all Illumina and Thermo Fisher platforms)
  • qPCR / dPCR
  • Sanger sequencing
  • Oligo synthesis
  • Gene synthesis
  • DNA / RNA extractions
  • Bioinformatics
  • Bio-banking
  • Logistics
You are in good company – we are approved by our prees

Eurofins Genomics is a trusted brand around the globe

Eurofins genomics is a trusted brand around the globe

We cooperate with almost all of the TOP 20 Big Pharma companies

We cooperate with renowned organisations ranging from small-, medium- and large-scale enterprises to academic institutions. We provide leading expertise and sequencing capabilities that are needed to address some of today’s most important scientific and technical challenges.

We are scientific partners with

We are cooperation partners with

We are scientific partners with

We are cooperation partners with

Our Logistic Solutions provide:

Simple and straightforward sample taking and shipment

SIMPLE SAMPLE TAKING
We send you kits with easy-to-follow instructions on how to take samples.

CONVENIENT SAMPLE SHIPMENT
Send back the kits directly or use our dropboxes for shipping.

Make use of our global network of logistics partners and send your samples safely.

Your dedicated Pharma Expert

Frédéric Antigny, MSc., MBA

Director Pharma & Translational Genomics Markets, Europe

Quality is our second name

Work with fully certified partner

ISO 17025 certified

ISO 17025

Guaranteed confidentiality and integrity of testing data.


Testing results are recognised by authorities and customs, etc. for the release of pharmaceuticals and food and feed, in the case of legal implications.

ISO 13485 certified

ISO 13485

Full documentation and traceability of production processes.


Compliance with regulatory requirements in regard to EU, US and other national directives about medical devices, in vitro Diagnostics or medicinal products.


Quality management system is in line with the FDA QSR standards.

GCLP

Guaranteed confidentiality and integrity of clinical trial data.


Full protection of patient rights, safety and well-being.


Full compliance with GCLP regulatory requirements.


Acceptance of clinical study data by regulatory authorities in EU, US and worldwide.

ISA GLP certified

GLP

Full traceability of GLP study data.


GLP compliant archiving of study data and records.


Full compliance with GLP regulatory requirements (OECD, EMA, US-FDA, US-EPA).


Acceptance of non-clinical safety study data by regulatory authorities in EU, US and worldwide.

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