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.
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.
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.
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.
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.
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.
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.
| Address | 15 Research Park Drive, St. Charles, MO 63304, USA |
|---|---|
| Tel | +1 844-522-7787 (main) |
| Website | https://apac.eurofinsdiscovery.com/ |
In non-clinical development, the choice of contract research organization shapes the quality of the data and the time it takes to reach the next decision. Below, three CROs are introduced by the type of study they support: pharmacology (efficacy) studies, safety studies, and pharmacokinetic (PK/PD) studies. Each summary describes the services the company offers so that you can match a provider to your target and development objective.
SMC Laboratories is a specialized non-clinical CRO focused on in vivo pharmacology and efficacy studies using disease-relevant animal models, particularly in fibrosis, inflammation, metabolic diseases, and oncology.
SMC Laboratories offers models covering the liver, lung, kidney, intestine, and oncology. Its portfolio includes the proprietary STAM™ model for MASH, fibrosis, and hepatocellular carcinoma.
Study plans are developed around the target biology, mechanism of action, disease stage, and development objective. Pharmacological endpoints can be combined with histopathology, biomarkers, and disease-specific readouts.
With experience from more than 1,000 studies for clients in 30 countries, SMC Laboratories supports programs from target validation and candidate selection through in vivo proof-of-concept studies.
Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.
Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.
Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.
Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.
Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.
PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.
Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.
Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.