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.
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.
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.
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.
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 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
| Address | 2638-2 Osaki, Koga City, Ibaraki Prefecture, Japan |
|---|---|
| Tel | 0280-76-4477 |
| Website | https://www.hamri.co.jp/ |
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.