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SAPPORO GENERAL PATHOLOGY LABORATORY Co.,Ltd.

Table of Contents
Table of Contents

SAPPORO GENERAL PATHOLOGY LABORATORY Co.,Ltd. specializes in contracted histopathological evaluation for nonclinical studies using disease models. The laboratory is recognized for detailed scoring evaluations across multiple organs and disease areas.

Features of SAPPORO GENERAL PATHOLOGY LABORATORY Co.,Ltd.’s Contract Services for Non-Clinical Studies

Specimen preparation with a broad range of staining techniques

For histopathology specimen preparation, the laboratory supports Hematoxylin and Eosin (H&E) staining, over 40 types of special stains, and immunostaining using over 200 primary antibodies. Specimens can be prepared from fixed organs and frozen blocks, and the team can provide unstained sections as well as quantitative image analysis (e.g., positive cell counts and area measurements).

The company flexibly accommodates study needs across research phases, from non-GLP to GLP studies.

Highly reliable, GLP-compliant testing framework

The laboratory has maintained a compliant (formerly “A”) rating in pharmaceutical GLP for over 30 years. Conformity evaluations have also been obtained for medical device GLP and chemical substance GLP, enabling safety and toxicity testing across a wide range of fields.

It provides highly reliable nonclinical testing services through a GLP-compliant framework and a proven track record.

From basic research to disease-model evaluation

The company receives requests from universities, pharmaceutical companies, and research institutes, and handles numerous pathology studies for basic research and pharmacology studies. Histological evaluation of disease models is also available.

Flexibility to handle small-batch requests and non-GLP studies is one of the laboratory’s strengths.

Example Disease Model at SAPPORO GENERAL PATHOLOGY LABORATORY Co.,Ltd.

NASH model / methionine- and choline-deficient (MCD) diet model

The methionine- and choline-deficient (MCD) model is one of the NASH models applied in the liver disease field. Using Hematoxylin and Eosin (H&E) staining, steatosis, lobular inflammation, and ballooning are each scored and quantified as the NAFLD Activity Score (NAS).

Fibrosis staging with Azan staining and related techniques can also be used to evaluate disease progression, including assessment up to cirrhosis. The model is highly reproducible and is commonly used in nonclinical studies for efficacy evaluation.

Reference URL: https://www.sgpl.co.jp/d_efficacy.html

Non-Clinical Case Study — SAPPORO GENERAL PATHOLOGY LABORATORY Co.,Ltd.

Histopathological evaluation across diverse disease models

The laboratory supports histopathological evaluation studies across a wide range of disease models, from kidney disease to dermatologic disease to neurodegenerative diseases.

For example, in the NASH model above, combining the NAFLD Activity Score (NAS) with the fibrosis stage enables detailed analysis of steatosis and fibrosis progression. In arthritis models, pathological findings such as bone destruction, cartilage loss, and synovial membrane thickening are graded to determine therapeutic efficacy. Quantitative evaluation using immunostaining and image analysis is also available.

See: https://www.sgpl.co.jp/d_efficacy.html

SAPPORO GENERAL PATHOLOGY LABORATORY Co.,Ltd. Company Information

Address3-17, Minami 12-jo Nishi 18-chome, Chuo-ku, Sapporo, Hokkaido
Tel011-563-6215
Websitehttps://www.sgpl.co.jp/index.html
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