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Oncodesign Services

Oncodesign Services is a leading contract research organization (CRO) specializing in drug discovery and preclinical research, with operations in France, Canada, and the United States.
This article provides an overview of the company’s preclinical contract research services and its extensive portfolio of disease models supporting translational drug development.

Features of Oncodesign Services’ Contract Services for Non-Clinical Studies

Expertise in Pharmacokinetics and Drug Metabolism (DMPK/ADME)

Oncodesign Services’ DMPK division conductscomprehensive studies in pharmacokinetics and drug metabolism (DMPK/ADME)for novel therapeutic candidates. Leveraging extensive experience across a wide range of drug discovery programs, the company delivers tailored and scientifically robust ADME/DMPK solutions to support informed decision-making throughout preclinical development.

Advanced Pharmacological and Molecular Imaging Capabilities

The company offersadvanced multimodal and nuclear imaging technologies, enabling detailed visualization of drug biodistribution, pharmacological efficacy, and biomarker responses in vivo. In addition, Oncodesign Services has strong expertise in molecular radiotherapy research, including radiolabeling of small molecules and antibodies, providing valuable insights into therapeutic targeting and mechanism of action.

In-house ABSL-2 and ABSL-3 Facilities

To address emerging infectious diseases that pose global public health threats, Oncodesign Services provides dedicated platforms supporting the development of therapeutic and preventive strategies.The company operates in-house ABSL-2 and ABSL-3 (Animal Biosafety Level) facilities, allowing studies involving high-risk pathogens such as SARS-CoV-2 and Mycobacterium tuberculosis.

Animal welfare is a core priority, and all in vivo studies are conducted under strict oversight in accordance with international ethical and regulatory guidelines.

Examples of Disease Models Available at Oncodesign Services

Oncodesign Services maintains a diverse portfolio of disease models designed to closely reflect human pathophysiology.
In the field of autoimmune disease research, the company offers both industry-standard and specialized models, including:
- Collagen-induced arthritis (CIA) models in mice and rats
- Acute experimental autoimmune encephalomyelitis (EAE) / multiple sclerosis (MS) models in mice
- Relapsing–remitting EAE / MS models in mice

In addition, the company provides preclinical CRO services focused on inflammatory liver diseases, including rodent models of hepatic inflammation.

Oncodesign Services Non-Clinical Case Study

Liver Fibrosis Research

The carbon tetrachloride (CCl₄)-induced liver fibrosis model is a widely established preclinical model. Repeated administration of CCl₄ to young mice typically induces liver fibrosis within approximately six weeks.

This model is well suited for evaluating therapeutic approaches targeting collagen deposition and regulation of matrix metalloproteinase expression. ALK5 inhibition, a well-characterized anti-fibrotic mechanism known to reduce collagen induction, is commonly used as a reference compound in these studies.

Reference: Oncodesign Services official website (https://www.oncodesign-services.com/inflammation/liver-models/)

Oncodesign Services Company Information

Founded in 1955, Oncodesign Services isa global CRO focused on drug discovery and preclinical research.With operations in France, Canada, and the United States, the company supports the development of innovative therapies across oncology, immunology, inflammatory diseases, and infectious diseases.

Address20 rue de la Fleuriée, 21000 Dijon, France
Tel+33 (0)3 80 78 82 60
Websitehttps://www.oncodesign-services.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