A site where you can find recommended contractors for non-clinical testing|effical " Non-Clinical CROs and Agencies " Labcorp Holdings Inc.

Labcorp Holdings Inc.

Table of Contents
Table of Contents

Labcorp provides contract services across the entire pharmaceutical industry—from early drug discovery to non-clinical and clinical studies, and pharma manufacturing. Through their in-house non-clinical testing platform, the company delivers a broad portfolio of highly specialized evaluation services on a global scale.

Features of Labcorp Holdings Inc.’s Non-clinical Contract Services

Global laboratory network and expert scientific teams

Leveraging an extensive worldwide network of non-clinical laboratories, Labcorp Holdings Inc. provides integrated support for a wide range of drug discovery research activities. Highly experienced scientists and specialists deliver multi-dimensional support, enabling flexible responses to diverse client needs in the preclinical field.

Labcorp Holdings Inc. serves as a reliable development partner for pharmaceutical companies and biotech ventures alike.

End-to-end development support—from early discovery to regulatory submission

Labcorp Holdings Inc. has established a system capable of providing seamless support at every stage of drug development—from the creation of drug candidate compounds to IND/CTA submissions and marketing applications.

Their services cover key components such as DMPK/ADME testing and toxicity evaluations, contributing to efficient and streamlined pharmaceutical development.
This end-to-end capability makes Labcorp Holdings Inc. an ideal partner for companies seeking to outsource comprehensive preclinical programs from the ground up.

Broad testing portfolio with strengths in pharmacokinetics, toxicology, and safety

Labcorp Holdings Inc. offers highly specialized preclinical studies, including DMPK/ADME evaluations, toxicology, safety pharmacology, and reproductive and developmental toxicity (DART). The company maintains robust in vitro and in vivo data acquisition platforms, along with GLP-compliant testing environments.

These capabilities ensure to gain high-precision preclinical data, which is essential for drug discovery.

Example Models Available at Labcorp Holdings Inc.

Rabbit model for DART studies

Labcorp Holdings Inc. conducts reproductive and developmental toxicity studies using rabbit models within DART evaluations to assess prenatal and postnatal toxic effects.

Rabbits are a standard species for teratogenicity studies due to their high sensitivity during fetal development, and they are considered to provide data with strong human correlation.

In compliance with GLP standard, Labcorp Holdings Inc. designs dosing schedules covering the entire gestation period and performs comprehensive assessments of both maternal and fetal parameters, supporting appropriate drug risk evaluation.

Reference:Labcorp Holdings Inc.
https://jp.labcorp.com/biopharma/nonclinical/disciplines/toxicology/dart

Labcorp Holdings Inc. Non-clinical Case Studies

DMPK characterization support for drug candidate compounds

Labcorp provides both in vitro and in vivo DMPK studies to support compound selection in the early stages of drug discovery.

In addition to CYP inhibition studies, protein binding assessments, and permeability/transport evaluations (PAMPA, Caco-2, etc.), Labcorp also conducts PK studies in multiple species, including mouse, rat, dog, and monkey.
Study designs can incorporate considerations such as gastrointestinal absorption and hepatic first-pass metabolism, helping accelerate the evaluation of candidate compounds.

Reference:Labcorp Holdings Inc.(https://jp.labcorp.com/biopharma/nonclinical/disciplines/metabolism)

Company Information

Address11F Harumi Triton Square Office Tower Y, 1-8-11 Harumi, Chuo-ku, Tokyo
Tel03-6837-9530
Websitehttps://jp.labcorp.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