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.
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.
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
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.
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. 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.
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.
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/ |
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.