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Mediford

Table of Contents
Table of Contents

Mediford offers a comprehensive range of non-clinical research services, including various safety studies required for regulatory submissions, pharmacology and pharmacokinetics studies. This page provides an overview of the key features of Mediford’s non-clinical service capabilities, examples of disease models, and representative study cases. It is intended to serve as a reference for selecting a CRO.

Features of Mediford’s Contract Non-Clinical Research Services

Extensive Study Portfolio

Mediford provides a wide variety of non-clinical studies, including pharmacology, safety, and pharmacokinetics studies. The company offers end-to-end support—from exploratory screening and new modality evaluation to transition into clinical development and regulatory submission. They offer flexible and efficient study execution with their dedicated project management system.

Highly Qualified Specialists

Mediford has JSTP/ JCVP-certified specialists in toxicology and pathology, as well as veterinarians, pharmacists, laboratory animal technologists, and JSOT-certified toxicologists. Their expertise enables high-quality data generation and supports establishing new evaluation protocols for emerging modalities and novel therapeutic concepts.

Commitment to Animal Welfare

All studies follow the 3Rs (Replacement, Reduction, Refinement) principles. Mediford implements microsampling techniques to analyze drug concentrations with minimal blood volume, reducing the number of animals required. The company is fully cerfitied by AAALAC International.

Infectious Disease Model Development and Evaluation

With ABSL2 and BSL2 facilities, Mediford conducts the full spectrum of infectious disease studies—from establishing a new model with viruses, bacteria, and fungi to efficacy and vaccine evaluation. Experienced researchers will deliver timely and reliable data to support your needs.

Examples of Disease Models Offered by Mediford

It is essential to go through the testing of candidate compounds in animal models that reproduce the target disease before advancing to clinical trials.

However, clinically relevant disease models may not always exist, thus there are demands for animal models with strong clinical correlation.

Below are some examples of disease models offered at Ina Research.

LPS-Induced Depression Model

A depression model is induced by administering lipopolysaccharide (LPS) to mice. Antidepressant effects can be evaluated by behavioral tests(forced swim, tail suspension, where immobility time serves as an indicator.)

Post-Stroke Pain Model

Post-stroke central pain is a persistent and debilitating complication of stroke. In this model, collagenase IV is microinjected into the ventral posterolateral nucleus of the thalamus in SD rats to induce intracerebral hemorrhage and reproduce CPSP pathology.

PDX Model (Oncology)

The PDX (Patient-Derived Xenograft) model is established by transplanting patient-derived tumor tissue into immunodeficient mice. Because tumor characteristics such as genetic mutations and microenvironment are preserved, PDX models are widely used in efficacy testing of anticancer and molecular-targeted therapies, as well as personalized medical research.

Reference: Mediford Official Website(https://www.mediford.com/service/topics/pdx/)

Ischemic Heart Disease Model

Myocardial infarction models in rats and mice are created by temporarily occluding and reopening the coronary artery to reproduce ischemia–reperfusion injury. Cardiac function is assessed using high-resolution ultrasound imaging (Vevo F2), allowing non-invasive analysis of left ventricular ejection fraction and wall motion.

GVHD Model

The graft-versus-host disease (GVHD) model reproduces the pathology in which donor immune cells attack host tissues after hematopoietic stem cell transplantation. The model is widely used to evaluate immunosuppressants and cell-based therapies.

Mediford’s Non-Clinical Study Examples

Neuropathic Pain Model Development

Neuropathic pain is a chronic condition caused by peripheral or central nerve injury. Mediford has extensive experience with the Bennett (thermal, mechanical, cold stimuli), Chung (thermal, mechanical), and Seltzer (thermal, mechanical) models, enabling reliable and reproducible pharmacology studies.

Skin Permeability Test in Compliance with GLP for Pesticides

In vitro skin permeability studies evaluate the penetration and transdermal transfer of test substances using human or animal skin. When combined with in vivo rat dermal administration studies, human in vivo absorption rates can also be estimated. Study results required for pesticide registration, including re-evaluation, are generated under pesticide GLP standards.

Company Information

Mediford provides medical writing services and contract research services, which utilize wide range of pathological models. They have decades of experience in non-clinical research.

Address 36-1 Shimizu-cho, Itabashi-ku, Tokyo
Tel 03-5943-9270
Website https://www.mediford.com/
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 official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories 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 is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
labcorp
(Labcorp Drug Development)
labcorp
Reference: labcorp official website (https://jp.labcorp.com/)
  • labcorp 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’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
PhoenixBio
Source: PhoenixBio Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio 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 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 delivers unmatched analytical precision and consistency.

Consult Phoenix Bio for PK/PD analysis with a clinical focus
By region
list of animal models
Expertise & Track Record
3 Recommended CRO for Non-Clinical Studies