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Japan SLC,Inc.

Table of Contents
Table of Contents

Japan SLC conducts non-clinical studies in-house, including GLP-compliant safety studies and pharmacological efficacy evaluations using a wide range of disease models, in addition to supplying laboratory animals.

As a fully integrated contract research organization, the company provides comprehensive support from animal breeding to antibody production.

Features of Japan SLC,Inc.’s Contract Services for Non-Clinical Studies

GLP-Compliant Safety Studies

Japan SLC,Inc. conducts in-vitro and in-vivo safety studies in compliance with the GLP standard for pharmaceutical drugs and medical devices.
Testing includes cytotoxicity, acute toxicity, and pyrogenicity evaluations, as well as studies aligned with GMP and QMS standards for target products.

With a flexible testing framework, the company can accommodate both GLP and non-GLP studies, supporting research from the early development phase through commercialization.

Flexible Study Design with Extensive Disease Models in Animal

Japan SLC,Inc. possesses a diverse portfolio of disease models in animals —including diabetes (STZ-induced), hyperlipidemia, arthritis, and pulmonary fibrosis—enabling tailored study designs depending on clients’needs.
In addition to models that are induced by diet, surgical, and chemical, the company also conducts specialized studies using ferrets and rabbits.

Japan SLC,Inc. not only performs contract studies but also supplies these disease model animals for external research uses.

Comprehensive Capability in Animal Supply and Antibody Production

The company offers end-to-end services covering the entire research process—from supplying and breeding laboratory animals to conducting pharmacological, safety, and pharmacokinetic studies, and antibody production.
Both polyclonal and monoclonal antibodies can be produced, with additional services such as splenocyte or PBMC collection available.

This integrated system enables Japan SLC,Inc. to deliver animals, technologies, and testing systems in one streamlined package, customized to the clients’ research goals and timelines.

An Example of Disease Model Provided by Japan SLC,Inc.

OSK-KI: A Genetically Engineered Mouse Model for Alzheimer’s Disease Research

The OSK-KI (C57BL/6-Tg(OSK-KI)) is a genetically modified mouse designed to overproduce amyloid-β, serving as a highly reproducible model for Alzheimer’s disease research.

A patent application has been filed for the model, which is recognized for its clinical translatability. The use of the model requires a research license agreement depending on the intended application.

Japan SLC,Inc. provides a wide range of advanced genetically engineered animal models to support drug discovery and disease mechanism studies.

Reference: Japan SLC,Inc. official website (http://www.jslc.co.jp/animals/mouse.php)

Example of Non-Clinical Study Conducted by Japan SLC

Pharmacological, Pharmacokinetic, and Immunological Studies Using Various Disease Models

Japan SLC,Inc. conducts a wide array of non-clinical studies utilizing animal models such as STZ-induced diabetes, drug-induced arthritis, and pulmonary fibrosis diseases.

Both GLP and non-GLP studies are available, including immunogenicity (antibody production) assessments.

Study designs can be flexibly tailored to the research purpose and development stage.

Reference: Japan SLC,Inc. official website http://www.jslc.co.jp/service/tests.php

Company Information

Address3371-8 Koto-cho, Chuo-ku, Hamamatsu City, Shizuoka, Japan
Tel053-486-3155
Websitehttp://www.jslc.co.jp/
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