Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » Nemoto Science Co.,Ltd.

Nemoto Science Co.,Ltd.

Nemoto Science Co.,Ltd. is a CRO specializing in contract pharmacokinetic (PK) studies and compound synthesis.This page provides an overview of the company’s non-clinical capabilities, representative study models, and case studies.
We have summarized information below for a reference.

Features of Nemoto Science Co.,Ltd.’s Non-clinical Contract Services

Wide Range of Study Capabilities

Nemoto Science Co.,Ltd. offers a GLP-compliant broad spectrum of studies that span from drug discovery through preclinical development.
The company handles numerous animal species—from small animals(mice and rats) to medium and large species(rabbits and non-human primates) —and offers both in vivo and in vitro studies.

Advanced Technologies and Equipment

Nemoto Science Co.,Ltd. performs detailed analyses using RI tracer studies with a wide range of radioisotopes (14C, 3H, 125I, 32P, 51Cr, etc.) and advanced analytical instruments including LC-MS/MS.
The company has introduced state-of-the-art technologies such as Orbitrap-based analysis of RI-dosed samples and metabolite identification via HPLC on-line LSC.
Specialized technical capabilities

Reliable GLP Compliance

Since the first GLP compliance inspection in 1998, Nemoto Science Co.,Ltd. has received an “A” or “Compliant” rating in every subsequent inspection. All of their studies are conducted at GLP-compliant facilities, enabling the company to generate high-quality and reliable non-clinical data for regulatory submission.

Partnered CROs with Nemoto Science Co.,Ltd.

Mediford Corporation

Mediford offers a comprehensive range of services, such as regulatory safety studies, pharmacology studies, pharmacokinetic studies, and supports exploratory research during the early stages of R&D.
Their facilities are not compliant with pharmaceutical GLP, medical device GLP, regenerative medicine GLP, agricultural chemical GLP, or the Chemical Substances Control Law GLP. Nemoto Science Co.,Ltd. is partnered with Mediford for specialty non-clinical pharmacokinetic studies.

Nemoto Science Co.,Ltd. Non-clinical Case Studies

In Vivo Pharmacokinetic Studies

Nemoto Science Co.,Ltd. offers development-appropriate in vivo PK studies at GLP-compliant facilities. They are capable of handling small animals (mice, rats, guinea pigs) as well as rabbits, dogs, and non-human primates.
Capabilities include RI tracer studies using various isotopes (14C, 3H, 125I, 32P, 51Cr) and analytical studies with LC-MS/MS and related platforms.
Study protocols and final reports can be prepared in both English and Japanese upon request.

Reference: Nemoto Science Co.,Ltd. official website https://www.nemotoscience.co.jp/souyaku

In Vivo PK Studies (Absorption, Distribution, and Excretion)

With decades of expertise in animal experimentation, Nemoto Science Co.,Ltd. provides reproducible and reliable data for absorption, distribution, and excretion studies.
Absorption studies include measurements such as blood and plasma concentration profiles, identification of gastrointestinal absorption sites, and evaluation of portal vein absorption.
For distribution studies, they can provide tissue distribution assessments, micro-autoradiography, placental transfer studies, and plasma protein binding evaluations.
In Excretion studies, urinary, fecal, biliary, and exhaled elimination can be evaluated.

Reference: Nemoto Science Co.,Ltd. official website https://www.nemotoscience.co.jp/souyaku

Company Information

Nemoto Science Co.,Ltd. has performed studies for many pharmaceutical companies for pharmacokinetic studies using tritium-labeled compounds, as well as contract synthesis and testing throughout the discovery and development phases.

Address 4-10-9 Takaido Higashi, Suginami-ku, Tokyo
Tel 03-3333-2711
Website https://www.nemotoscience.co.jp/

3 Recommended Contract Research Organizations
for Non-Clinical Studies
— by Target goal and Expertise

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.

Pharmacology (Efficacy) StudiesDisease-Relevant Models for
Translational Drug Evaluation
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/)

SMC Laboratories, Inc.

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.

Areas of Expertise
Disease-Relevant Model Portfolio

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 Design Based on Target Biology

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.

Support from Target Validation to Proof of Concept

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.

Safety StudiesComprehensive Safety Assessment for
Preclinical Development
Charles River Laboratories
Reference: Charles River Laboratories official website (https://www.criver.com/)

Charles River Laboratories

Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.

Areas of Expertise
General Toxicology Across Study Designs

Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.

Non-GLP and GLP Study Support

Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.

Integrated IND-Enabling Safety Assessment

Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.

Pharmacokinetic (PK/PD) StudiesConnecting Drug Exposure with
Pharmacological Response
Inotiv
Reference: Inotiv official website (https://www.inotiv.com/)

Inotiv

Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.

Areas of Expertise
Pharmacokinetic Characterization

PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.

Exposure–Response Evaluation

Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.

Integrated DMPK and Development Support

Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.

By Therapeutic Area
Disease Animal Models
and Reviews
Proven Capability, Expertise and Track Record
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