Integrated Lab Performance and BioPharma Solutions From the Organization You Trust

From compound discovery and clinical research through manufacture and release of commercial product and post approval/marketing, Eurofins BioPharma Services provides seamless, end-to-end solutions to help clients progress through the drug development cycle through a single, experienced provider. Our integrated solutions deliver the most comprehensive range of state-of-the-art analytical technologies with an expansive geographic reach in order to support our clients’ specialized testing needs and stringent quality and safety requirements around the world.

Product Discovery

A Strong Foundation for Successful Drug Discovery

Eurofins Discovery offers you a complete, single-source solution for drug discovery products and services. We are rooted in the deep expertise and best-in-class offerings of 6 premier CROs: Cerep, DiscoverX, EMD Millipore Drug Discovery Solutions, Panlabs, Selcia Drug Discovery, and Villapharma.

Eurofins Discovery can optimize your discovery process – whether you need complete, end-to-end services, help with one or more stages, or the products for discovery work.

With over 600 scientists around the world, 50 patents, and 30 billion data points screened, you can rely on Eurofins Discovery to provide you with the deep resources needed for your success.

• Standalone Services. Offering the ability to support your projects on an as-needed basis across the drug discovery workflow, Eurofins Discovery offers you services for Medicinal Chemistry, Synthetic Chemistry, In Vitro Pharmacology, Safety & Efficacy, ADME & Toxicology, and Phenotypic Assays. In Vivo services are available through our partner lab, Pharmacology Discovery Services.
• Integrated Drug Discovery. The DiscoveryOne™ integrated drug discovery team works hand-in-hand as partners with you, integrating all Eurofins Discovery capabilities to accelerate delivery of preclinical candidates by utilizing our in-house project management and deep scientific expertise.
• Products for Drug Discovery. Eurofins DiscoverX, a Eurofins Discovery company, is the trusted product solutions provider that can accelerate your programs with confidence with qualified reagents, cell lines, and assays ready to run today. Eurofins DiscoverX develops and manufactures cutting-edge assays, stable cell lines, membrane preps, enzymes, and reagents for drug discovery and development.
• Eurofins Discovery provides global drug discovery support in USA, Europe, and Asia.

Product CDMO

Your Drug Development Partner

Eurofins CDMO provides a sustainable and flexible solution for pre-clinical and clinical development and manufacturing services for Drug Substance/API and Drug Products (Biologics and Small Molecules). Eurofins CDMO has state-of-the-art facilities in North America, Europe and India.

Science represents the foundation of our business and allows Eurofins CDMO to support small and major biopharmaceutical companies through a sustainable and flexible method to help them achieve their pre-clinical and clinical milestones on time.

We are experts in breakthrough technologies for highly potent compounds, poorly soluble drugs, lyophilisation processes and specific therapeutic areas (immunotherapies, orphan drugs, paediatric dosage forms, etc.) Involved in the earliest steps, our highly-qualified project management team will effectively communicate a complete drug development strategy to help meet your timelines.

Eurofins CDMO offers a vast range of services:

• Drug Substance/API development
• Solid State Research & Development
• Pre-Formulation and Formulation development
• GMP manufacturing
• Clinical packaging and logistics
• Project management and CMC RA
• Operating under strict quality procedures, Eurofins CDMO is accredited through the FDA, EMA, ANSM, ANSES, FAMHP, PMDA, and Health Canada.

With more than 30 years of combined experience between all entities in preclinical and clinical development, our expert teams ensure your clinical trials achievements are:

• Supporting clients to move rapidly through the drug development value chain
• Performing complex formulation screening and development for sterile and non-sterile manufacturing
• Accelerating process development and scale-up under GMP compliance
• Supplying clinical trial material including packaging and logistics
• Complying with regulatory requirements throughout each stage of the development cycle with full CMC-RA support

Professional Scientific Services (PSS) Insourcing solutions

When you have the workload, but not the workforce.

PSS Insourcing Solutions® provides laboratory management services for Bio/Pharmaceutical companies who face workload/workforce challenges and require testing to remain at their facility. We place our people at our client’s facility dedicated to running and managing their laboratory services while eliminating headcount, co-employment, and project-management worries.

Founded under Eurofins Lancaster Laboratories, PSS infuses our 58-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices to recruit, hire, train, and manage highly qualified scientists to perform laboratory services at our client’s site, using their quality systems and equipment. Our teams will even help set up the laboratory and validate equipment according to the client’s SOPs and laboratory practices as needed.

We have proven success providing dedicated teams for a variety of technical disciplines that span the drug development pipeline, providing:

• The security of keeping your projects at your facility.
• Solutions to potential co-employment issues and challenges associated with staff augmentation.
• Metrics to demonstrate productivities, efficiencies, and cost savings.
• Lean laboratory best practices and training to save time, eliminate waste, and ultimately bring cost savings to our PSS clients.
• A resource for technical expertise and support through laboratory staff at our network of global facilities.
  We know how to find great people and take great care of them, so they in turn will take great care of our clients.

Clinical Bioanalytical Services

Biologics Done Right

Eurofins is a leading supplier of bioanalysis and DMPK solutions, with cutting-edge scientific expertise. We support discovery, preclinical and clinical studies providing method development, validation, and sample analysis in all biological matrices for both small and large molecule drug development. We offer a comprehensive range of PK/TK, ADME, ADA, NAb, biomarker assays and sample analysis to all sponsors in the world’s pharmaceutical and biopharmaceutical landscape.

We have a mission to support our clients with high quality Bioanalysis and DMPK results in both pre-clinical and clinical development. Our sole focus is providing the precision and accuracy in the data that our clients need for decision making, IND filings and product registrations in both small and large molecules, and biomarkers.

Eurofins Bioanalytical Services laboratories are at the forefront of novel approaches to overcome the most complex assay challenges and demonstrate industry leadership in developing, optimizing, validating and performing immunoassays and LC/MS/MS bioanalysis on human and animal specimens. We offer trusted bioanalytical solutions to support studies from preclinical non-GLP to IND-enabling Toxicity studies to multi-national Phase III clinical trials. We can take your drug from research through development to regulatory submission.

We offer:

• Scientific expertise supporting the widest scope in clinical trials with small and large molecule bioanalysis for PK/TK, ADA and cell-based NAb. Our services also include PK calculations and interpretation, bioequivalence studies, and biomarker assays.
• State-of-the-art laboratory facilities in the USA and France providing diverse platforms and technologies including LC-MS/MS and ELISA to address increasingly demanding client specifications.
• In-house development of small molecule assays, ELISA and ECL development, creation and analysis of antibody-drug conjugates.
• Dermal absorption studies [in vitro/in vivo]
• Advice from a highly qualified team, adaptability for all study designs, flexibility in timelines.
• The benefit of our experience with biotechs as well as with mid and large size pharma companies with an international recognition for the quality of our services.

Clinical Central Laboratory

Results That Matter

Reliable, high quality laboratory data is pivotal to the success of clinical trials. It’s the RESULTS THAT MATTER. We are dedicated to providing the most cost effective and efficient testing solutions to pharmaceutical and biotech companies, and CROs alike.

At Eurofins Central Laboratory, we are the End-to-End solution to the BioPharma industry! As a dedicated Laboratory CRO, we go above and beyond to provide an array of services to ensure that any clinical trial sample is collected, transported, managed, analyzed, reported and stored to meet the objectives and purpose of each study.
Deploying our 4 standardized, wholly-owned global locations in USA, the Netherlands, Singapore and China, we provide CAP/CLIA certified analytical services in both a GCP and GCLP environment. This allows us to combine safety and efficacy analysis with Biomarker Services embedded within one laboratory, introducing cost efficiencies into Sponsor study budgets, and increasing specimen integrity by reducing unnecessary transport. With Eurofins Central Laboratory acting as the hub, in a hub and spokes model, Sponsors will also have access to the extensive Testing Portfolio available within the Eurofins BioPharma Services Group.

What differentiates Eurofins Central Laboratory from the rest? Innovation. Whether that is our specimen visibility tool, EzRF (web based requisition), our home based, patient specimen collection kits or our mobile laboratory technician service for standardized CAP certified on-site analysis of rapid analytical TAT requirements (PBMC, semen analysis, virology specimen processing), Eurofins Central Laboratory is your analytical solution for Phase 1 to 4 clinical trials.

With over 20 years of experience in kit packing and distribution, Eurofins Central Laboratory offers Kit Packing and Distribution Services using wholly owned and fully harmonized Kit Packing facilities in the USA, Europe and China. Building on a proven track record of building and distributing study and visit-specific specimen collection kits in support of Clinical Trials, we also provide specimen collection kits for Commercial DNA Testing, Clinical Diagnostics, Clinical Monitoring Programs and Post Marketing Surveillance.

Clinical Anatomical Pathology

Specialized Medical Pathology

The deployment of pathology testing has become increasingly important in safety, vaccine and oncology trials. Pathology testing is facing similar challenges as central laboratory testing; large sample numbers distributed over many locations, a need for expert global logistics support to maintain specimen integrity, quick turnaround time of results and the necessity for globally combinable data.

With a keen eye on the specifics of a clinical trial, Eurofins Biomnis offers anatomic, clinical and molecular pathology services to assess traditional clinical-pathological factors as well as the molecular biological features of a given tumor to support safety, vaccine and oncology trials.

Eurofins Biomnis focuses mainly on specialised pathology testing, which requires highly skilled expertise, and which cannot be performed in routine private or hospital-based laboratories. Eurofins Biomnis specialises in all areas of pathology and testing is performed using the most recent and cutting-edge techniques, which necessitate complex calibrations and validations, highly qualified experts and sophisticated equipment.

• Surgical pathology
• Tumor confirmation and classification
• Pathology reads for efficacy
• Slide preparation and preservation
• Histology
• Cytology
• Molecular pathology
• FISH