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

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.

Essential Technologies

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

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 Solutions to your challenges

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

Pre-clinical screening

Clinical trials

Biomarkers

Toxico-genomics

Drug screening

Cell therapy and
manufacturing

Pharmaco-genomics

Metagenome & Microbiota

Antibodies & Amplicons

Oncology

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 few to millions 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 HANDS – WE ARE APPROVED BY YOUR PEERS

Eurofins Genomics is a trusted brand around the globe

We cooperate with renowned organisations ranging from small and medium-scale enterprises to 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.

Read about the latest company news

Our Logistics solutions Provide:

Simple and straightforward sample taking and shipment

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

CONVENIENT
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 genomics experts

Frédéric Antigny, MSc., MBA

Director Project Sales Europe

 
Quality is our middle name

Work with a fully certified partner

ISO 17025

  • Guaranteed confidentiality and integrity of testing data.
  • Testing results are recognised by authorities and customs, etc. for the release of pharmaceuticals, food and feed and in the case of legal implications.

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 wellbeing.
  • Full compliance with GCLP regulatory requirements.
  • Acceptance of clinical study data by regulatory authorities in EU, US and worldwide. 

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.
 
get in touch with our experts

Ask us anything. We are happy to help.

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