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Kamakura Techno‒Science, Inc.

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Table of Contents

Kamakura Techno‒Science, Inc. is a spin-off contract research organization(CRO) from Toray Industries’ research institution.
They are a GLP-compliant facility, the company conducts a wide range of non-clinical studies—Pharmacology(PD), Safety, and Pharmacokinetics(PK)studies—at their facilities.

Features of KamakuraTechno‒Science’s Non-clinical Services

Robust evaluation capabilities across multiple therapeutic areas

The company offers non-clinical pharmacological studies, which cover diverse disease areas. This includes Neurological, Cardiovascular, and Gastrointestinal related areas (Cerebral infarction, Diabetes, and Allergic dermatitis models). They use evaluation methods established through Toray Industries’expertise in pharmaceutical research.

Kamakura Techno‒Science, Inc. Science also provides numerous exploratory and PoC-supporting models, including L-DOPA–induced model and Pruritus model. You can expect their flexible and scientifically backed proposal for your non-clinical needs.

GLP-compliant drug safety assessment

KamakuraTechno‒Science provides non-clinical safety testing for a wide range of material, including pharmaceutical drugs, medical devices, or food additives.
The company is in compliance with GLP standards—Pharmaceutical GLP, Medical Device GLP, Chemical Substances Control Law GLP, and OECD GLP. —They offer extensive experience in general toxicity, genotoxicity, immunotoxicity, and biological safety testing.

Its capabilities also include skin sensitization/irritation testing, pyrogen testing, and other assessments required in the medical device development, delivering both regulatory compliance and high reliability.

High-precision pharmacokinetic analysis using LC/MS/MS

Using high-sensitivity LC/MS/MS platforms such as the SCIEX QTRAP® 6500, Kamakura Techno‒Science, Inc. performs high-precision drug concentration analysis for various biological materials.

The company supports both in-vitro and in-vivo pharmacokinetic assessments, including CYP inhibition/induction studies, metabolic stability studies, PK studies, and biliary excretion studies. In addition to GLP-compliant analysis, metabolite profiling and hemodialysis removal assessment are also available.
These high-quality, radioisotope-free data support accurate evaluation of drug’s safety and efficacy.

An Example Model Available at Kamakura Techno‒Science, Inc.

Neuropathic Pain Model (Chung Model)

The Chung model reproduces neuropathic pain caused by peripheral nerve injury and is widely used in evaluating analgesic drug candidates.
By ligating a portion of the sciatic nerve, mechanical allodynia and thermal hypersensitivity can be quantitatively assessed in the affected hindlimb.

Kamakura Techno-Science maintains multiple neurological disease models—including the Chung model, water-immersion stress model, and tremor model. They offer GLP-compliant testing to deliver highly reliable data.

Reference:
https://www.kamakura-ts.co.jp/test/pharmacology/index.html

Case study For a Non-clinical Study Conducted by Kamakura Techno‒Science, Inc.

Pharmacological study using a Pulmonary Fibrosis Model

The company conducts pharmacological evaluations in respiratory disease research using a well-established pulmonary fibrosis model.

Fibrosis is induced by repeated administration of bleomycin, enabling quantitative assessment of anti-fibrotic drug efficacy.
Study endpoints include lung function, histopathology, and inflammatory markers, providing comprehensive multi-angle evaluation.

GLP-compliant execution is also available, supporting clients’ drug development with reliable and reproducible data.

Reference:
https://www.kamakura-ts.co.jp/test/pharmacology/index.html

Company Information

Address6-10-1 Tebiro, Kamakura, Kanagawa, Japan (Toray Industries Basic Research Center)
Tel+81-467-32-9775
Websitehttps://www.kamakura-ts.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