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Nihon Bioresearch Inc.

Table of Contents
Table of Contents

Nihon Bioresearch Inc. is a contract research organization specializing in pharmacological efficacy studies and the development of numerous disease models. This page provides an overview of the company’s non-clinical study capabilities, examples of disease models, and selected study cases. Please use this information as a reference when selecting a CRO for non-clinical studies.

Features of Nihon Bioresearch Inc.’s Non-clinical Contract Services

Extensive Disease Models and Animal Species

Nihon Bioresearch Inc. has developed more than 300 disease models and evaluation studies are available across a wide range of areas, including pharmaceuticals, medical devices, regenerative medicine products, and functional foods.
The company offers study models with high translational correlation to humans, enabling accurate evaluation and supporting drug discovery and development. With various animal species, Nihon Bioresearch provides assessments based on a broad array of pathophysiological models in central nervous, metabolic, inflammation, and other indications.

Studies Using Miniature Pigs

The company provides a wide range of non-clinical studies using miniature pigs. It is conducted at a specialized GLP-compliant facility that can house up to 178 animals.
Miniature pigs, known for their strong translational correlation to humans, are used for pharmacology, pharmacokinetics, and safety studies in the cardiovascular, urological, allergic, and metabolic indications.

Comprehensive Evaluation of Central Nervous System Disorders

Nihon Bioresearch Inc. offers tailored CNS studies using multiple small-animal models for evaluating dementia, Parkinson’s disease, depression, anxiety, and related disorders. The company has focused particularly on developing cognitive impairment models such as the rotenone intranigral injection Parkinson’s model and the single intracerebroventricular dose α-synuclein model. A wide range of CNS models—including depression/anxiety, schizophrenia, and autism—can be used for drug efficacy assessment and pathophysiological analyses.

Contract Companies Handled by Nihon Bioresearch Inc.

No partner CROs were listed.

Nihon Bioresearch Inc. Non-clinical Case Studies

Pharmacology (Efficacy) Studies

Nihon Bioresearch Inc. offers a wide selection of animal models across multiple fields (CNS, respiratory/cardiovascular, metabolic, gastrointestinal, allergic, etc.).
The company can provide proposal study design and develop new models based on client needs.
Their strengths include studies using diverse animal species and advanced CNS evaluation protocols such as PCP-induced schizophrenia models, olfactory bulbectomy–induced depression models, and behavioral/functional analyses of genetically engineered animals.

Reference: Nihon Bioresearch Inc. official website https://www.nbr.co.jp/leaflet/pharmacol-cat/

Miniature Pig Studies

The company operates a dedicated facility capable of housing up to 178 miniature pigs for both breeding and experimental use.
Its track record includes pharmacology studies for cardiovascular, urological, allergic, and metabolic indication, pharmacokinetic studies of topical formulations, skin irritation testing, and repeated-dose toxicity studies.
Nihon Bioresearch Inc. offers study proposal that account for the characteristics and human translatability of miniature pigs.

Reference: Nihon Bioresearch Inc. official website https://www.nbr.co.jp/leaflet/pharmacol-cat/

Toxicology Studies

Nihon Bioresearch Inc. conducts reproductive and developmental toxicity studies, GLP-compliant studies in miniature pigs, adverse effect confirmation study, and testing of specialized medical devices.
The company offers models with various animal species and administration routes. They have experience performing all ICH Study 1, 2, and 3 studies, including those using transdermal administration.
Furthermore, their proprietary GLP/FDA Part 11–compliant preclinical data management system ensures the delivery of highly reliable data.

Reference: Nihon Bioresearch Inc. official website https://www.nbr.co.jp/leaflet/safety-cat/

Company Information

Nihon Bioresearch Inc. offers reproducible reliable contracted services with co-development and proposal driven approach for pharmaceuticals, medical devices, and regenerative medicine products.

Address 6-104 Majima, Fukuju-cho, Hashima-shi, Gifu, Japan
Tel 058-392-6222
Website https://www.nbr.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