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.
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.
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.
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.
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 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)
| Address | 11F Harumi Triton Square Office Tower Y, 1-8-11 Harumi, Chuo-ku, Tokyo |
|---|---|
| Tel | 03-6837-9530 |
| Website | https://jp.labcorp.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.