A site where you can find recommended contractors for non-clinical testing|effical " Non-Clinical CROs and Agencies " HAMRI CO., LTD.

HAMRI CO., LTD.

Table of Contents
Table of Contents

HAMRI is a GLP contract research organization (CRO) offering non-clinical study for pharmaceutical and regenerative medicine, fully AAALAC-accredited facilities.

The company has extensive expertise in various disease models and strong capabilities in providing support from the study design stage.

Features of HAMRI’s Non-Clinical Study Services

Comprehensive coverage of pharmacodynamics, safety, and pharmacokinetics

HAMRI undertakes all three core areas of non-clinical testing—pharmacodynamic studies, safety studies, and pharmacokinetic studies—in-house.
The company conducts efficacy evaluations in various animal models in diabetes, autoimmune diseases, and Parkinson’s disease.

Under GLP compliance, HAMRI also performs safety evaluations including toxicity and genotoxicity studies, as well as pharmacokinetic analyses of absorption, distribution, metabolism, and excretion (ADME).
With an integrated system that covers study design, data analysis, and report preparation, they offer flexible and tailored design for clients’ needs.

GLP-compliant facilities and full AAALAC accreditation

In addition to being fully GLP compliant, they are also fully accredited by AAALAC International, a global organization that evaluates and certifies laboratory animal care.
By combining scientific reliability with animal welfare, HAMRI has earned the trust of regulatory authorities and pharmaceutical companies both in Japan and globally.

They continue to implement various protocols to ensure high-quality and safe testing environment.

A wide range of disease models, including STZ-induced Type I diabetes

HAMRI provides a broad selection of animal models for various diseases, including STZ (streptozotocin)-induced Type I diabetes models.
They deliver highly accurate efficacy evaluations for specific disease targets.

In the diabetes model, they offer multifaceted evaluation parameters— change in blood glucose levels, insulin secretion level—which allow detailed verification of the efficacy and mechanism of action of candidate compounds.

Disease Model available at HAMRI

STZ-induced Type I diabetes mellitus in a crab-eating monkey model

HAMRI has Type I diabetes mellitus model in crab-eating monkeys.
This model is induced by streptozotocin (STZ), which is used for pharmacological efficacy studies.
As a diabetes model, detailed efficacy evaluations can be conducted based on multiple indications, changes in blood glucose and insulin secretion level.

They can also co-develop a long-term exploratory study with the same animal for prolonged period of time.

You can expect gaining valuable data for drug discovery or investigating disease mechanism of action. Standard analysis includes sample analyses using ELISA, real-time PCR, and FACS.

Reference:
https://www.hamri.co.jp/medicinal-effect

HAMRI’s Non-Clinical Study Case Example

STZ-induced Type I diabetes model in micromini pigs

HAMRI have developed STZ-induced Type I diabetes model in micromini pigs. They measure blood glucose levels over time.
In this study, a continuous glucose sensor was implanted subcutaneously to track the progression of diabetes in real time, demonstrating an innovative evaluation approach for new diabetes models that contributes to drug discovery research.

This is a valuable case study from HAMRI’s. It was recorded through an external presentation.

Reference:
https://www.hamri.co.jp/seminar02

Company Information

Address2638-2 Osaki, Koga City, Ibaraki Prefecture, Japan
Tel0280-76-4477
Websitehttps://www.hamri.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