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Eurofins Discovery Services North America LLC.

Eurofins Discovery Services North America LLC. is a global contract research organization (CRO) supporting drug discovery programs from early discovery through the preclinical stage. The company provides in-house safety, efficacy, and pharmacokinetic studies, offering an integrated, end-to-end solution spanning target identification through lead and candidate selection.
With proprietary laboratories and dedicated scientific teams, Eurofins Discovery Services North America LLC. delivers directly managed, high-quality nonclinical research services.

Features of Eurofins Discovery Services North America LLC.’s Contract Services for Non-Clinical Studies

Comprehensive off-target safety profiling

Eurofins Discovery Services North America LLC. offers extensive safety profiling through thousands of assays, including SafetyScreen™ and SAFETYscan®, enabling comprehensive evaluation of off-target activities of candidate compounds.
By integrating binding and functional analyses, potential safety liabilities can be identified early, reducing attrition risk during development.
In addition, data visualization via In Vitro Safety Insight allows intuitive assessment of organ-specific adverse responses.

High-precision ADME and pharmacokinetic evaluation

With access to more than 500 in vitro ADME and toxicity assays, Eurofins Discovery Services North America LLC. conducts detailed analyses of absorption, distribution, metabolism, and excretion properties.
Safety endpoints such as hepatotoxicity, nephrotoxicity, and cardiotoxicity are evaluated in parallel, supporting early-stage risk mitigation.
The resulting datasets contribute to more accurate candidate selection while helping to shorten development timelines and reduce overall costs.

Target characterization and efficacy assessment with LeadHunter™

Through the LeadHunter™ platform, Eurofins Discovery Services North America LLC. provides in vitro pharmacology assays covering key target classes including GPCRs, kinases, and ion channels.
Binding affinity and selectivity are rapidly assessed to support lead optimization.
The combination of high data reproducibility and fast turnaround enables efficient progression toward preclinical candidate selection.

Examples of Disease Models Available at Eurofins Discovery Services North America LLC.

MASH LeadHunter® Panel (PP318)

This panel includes major targets involved in glucose, lipid, and bile acid metabolism—such as THRβ, FXR, and PPAR—and enables comprehensive analysis of mechanisms of action from metabolic regulation to inflammation and fibrosis. It is well suited for MOA elucidation and early-stage screening in MASH drug discovery programs.

TGFβ-induced liver fibrosis cell model

Using the human hepatic stellate cell line LX-2, this model reproduces the fibrotic process induced by TGFβ stimulation. Antifibrotic efficacy can be evaluated using COL1A1 expression as a readout, making it a valuable in vitro model for assessing candidate therapeutics for MASH and liver fibrosis.

Eurofins Discovery Services North America LLC. Non-Clinical Case Study

Validation of functional assays for safety assessment

Using SAFETYscan® functional assays, 26 marketed drugs were evaluated across 17 liability targets and compared with radioligand binding data generated by Novartis.
The results demonstrated strong concordance between activity values obtained from both methods, while functional assays additionally enabled discrimination of mechanisms of action (MoA).
This case study highlights how incorporating functional safety assays at early discovery stages can facilitate early identification of off-target effects and improve candidate selection prior to animal studies.

Eurofins Discovery Services North America LLC. Company Information

Address 15 Research Park Drive, St. Charles, MO 63304, USA
Tel +1 844-522-7787 (main)
Website https://apac.eurofinsdiscovery.com/
3 Recommended Contract Research Organizations for Non-Clinical Studies
— by Target goal and Expertise

In drug discovery, the quality and efficiency of non-clinical studies have a direct impact on clinical success rates, development costs, and overall length of time required in R&D. In recent years, there has been more demand for clinically relevant data, globally accepted reliability, and accurate early-stage screening. Thus, it is more important than ever to select the right CRO (Contract Research Organization) for strategic approach.
In this article, we highlight three CROs with proven technical capabilities, expertise, and long standing track records. These are our TOP 3 choices based on their capabilities and the specific target goals of the researchers for their non-clinical studies.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories, Inc. has established a disease models using patented mouse technologies. The company has established proprietary pathological models—particularly in liver disease and fibrosis—and continues to expand their approach across a wide range of models in cancer, inflammation, and metabolic diseases.
  • From exploratory research to clinically oriented efficacy evaluation, SMC offers customized study designs, dosing strategies, and evaluation analysis tailored to each project. Their collaborative approachallows researchers to discuss and refine study plans together with SMC’s expert scientists.

  • With flexible small-scale study options and strong technical support, SMC Laboratories, Inc. is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
Labcorp Holdings Inc.
(Labcorp Drug Development)
Labcorp Holdings Inc.
Reference: Labcorp Holdings Inc. official website (https://jp.labcorp.com/)
  • Labcorp Holdings Inc. provides a fully integrated GLP testing system aligned with international regulatory standards, including FDA, EMA, and PMDA requirements. All studies are conducted under ICH-compliant quality assurance, making it ready for data submission.
  • The company has extensive expertise in long-term toxicity studies such as Segment I–III reproductive and carcinogenicity studies, as well as 2-year chronic toxicity assessments.
  • Labcorp Holdings Inc.’s comprehensive approach enables sponsors to efficiently outsource the entire preclinical package from toxicology, toxicokinetic (TK), and safety pharmacology study design to execution. This accelerates a path to First-in-Human (FIH) trials. For most of the global drug developers, this all-in-one service structure minimizes cost, risk, and expedite the time before advancing to clinical phase.
Pharmacokinetic (PK/PD) Studies
High-Precision Bioanalysis for Clinically Predictive PK/PD Evaluation
PhoenixBio Co., Ltd.
PhoenixBio Co., Ltd.
Source: PhoenixBio Co., Ltd. Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio Co., Ltd.offers pharmacokinetic and hepatic metabolism studies using their proprietary PXB-mouse®, a humanized-liver chimeric mouse model. This platform enables the acquisition of data with high clinical correlation in ADME, drug–to-drug interaction studies, bridging the gap between preclinical and clinical stages.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio Co., Ltd. provides aseamless workflow from plasma concentration measurement and metabolite identification to quantitative validation.

  • The company offersan integrated evaluation analysiscovering pharmacokinetics, hepatotoxicity, and safety with flexibility to accommodate complex modalities such as oligonucleotide and middle-molecule therapeutics. For compounds where hepatic metabolism is a development bottleneck—or where quantitative, reproducible exposure data are critical—PhoenixBio Co., Ltd. delivers unmatched analytical precision and consistency.

By region
list of animal models
Expertise & Track Record
3 Recommended Contract Non-Clinical Testing Services