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IQVIA Laboratories

IQVIA Laboratories is a company that provides integrated lab services covering from the early stages of drug discovery to the clinical phase. For non-clinical studies, in addition to conducting tests in-house, they have a system in place to support the entire development process by handling everything from custom model development to analysis. This section introduces the features of IQVIA Laboratories' non-clinical studies.

Features of IQVIA Laboratories' non-clinical testing contract services

Flexible study design centered on custom in vivo model development

One of the significant strengths of IQVIA Laboratories' preclinical testing services is its flexible study design capabilities, centered around the development of custom in vivo models. Rather than relying on existing standard models,Design and construct appropriate disease models according to the target disease, mechanism of action, and endpoints to be evaluated.We have established a system to support research. We cover a wide range of fields, including infectious diseases, tumors, and immune disorders, and can modify models and optimize conditions according to research objectives. Furthermore, specialists in immunology and molecular biology are involved from the study design stage to construct an integrated evaluation system that combines in vivo studies with various bioassays. We achieve the generation of highly reproducible and practical data, with a view to bridging from early drug discovery to clinical application.

Improving Development Efficiency with High-Throughput ADME and Bioanalysis

By combining high-throughput ADME (Absorption, Distribution, Metabolism, Excretion) testing with advanced bioanalysis, we improve development efficiency in the preclinical stage. Leveraging automated testing platforms,Rapid and parallel evaluation of numerous compoundsThis allows for the early screening of promising candidates. By comprehensively analyzing metabolite identification, drug-drug interactions, and biomarker measurements, drug properties can be understood from multiple angles. A system is in place to reduce risks after clinical transition and expedite decision-making, thereby supporting the overall efficiency of the drug discovery process.

GLP-compliant global testing system that meets international standards

We have established lab operations that comply with GLP (Good Laboratory Practice) and a testing system that meets international standards.We can provide high-quality data with regulatory submission in mind.All types of studies, including bioanalysis, are conducted under standardized procedures to ensure data reliability and reproducibility. Furthermore, our animal testing facilities are operated in consideration of international guidelines, meeting the standards required for global development. By leveraging our global network of facilities, we can design studies and build data packages that comply with regional regulatory requirements. We support efficient project advancement for international joint development and country-specific applications.

Example of a disease model owned by IQVIA Laboratories

LCMV infection model (Lymphocytic choriomeningitis virus)

LCMV models areRepresentative in vivo models for evaluating immune responses to viral infectionsIQVIA Laboratories utilizes it as a challenge study in a BSL-2 environment, serving to evaluate the efficacy of vaccines and immunotherapies. A key feature is its ability to analyze both cellular immunity (T-cell response) and humoral immunity. It is positioned as a foundational model for preclinical evaluation in the infectious disease field.

Tumor Growth Model

Oncogenic proliferation modelsAn in vivo model for evaluating the efficacy of anticancer drugs and immune checkpoint inhibitorsAt IQVIA Laboratories, treatment efficacy is verified using indicators such as tumor growth inhibition and changes in immune response. This is particularly utilized in the field of immuno-oncology for analyzing drug mechanisms of action and exploring combination therapies. It plays a crucial role in evaluating efficacy during the preclinical stage.

IQVIA Laboratories Non-Clinical Study Examples

Information on non-clinical study examples was not available on the official website.

IQVIA Laboratories Corporate Information

Address IQVIA Laboratories Japan K.K.: 2-5-10 Aomi, Koto-ku, Tokyo, Telecom Center Building
Tel 03-6859-9620
Website https://www.iqvia.com/ja-jp/locations/japan
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