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Sekisui Medical Co.,Ltd.

Table of Contents
Table of Contents

Sekisui Medical Co.,Ltd. (hereinafter referred to as “Sekisui Medical”) is a contract research organization (CRO) specializing in nonclinical pharmacokinetic studies using radiolabeled compounds. This overview presents the characteristics of Sekisui Medical’s nonclinical studies, representative disease models, and case examples. Please use it as a reference when selecting a CRO for nonclinical studies.

Non-Clinical Studies at Sekisui Medical

Pharmacokinetic studies using radiolabeled compounds

They have strong capabilities in absorption, distribution, metabolism, and excretion (ADME) studies utilizing radiolabeled compounds (e.g., 14C, 3H). Their technology supports prediction of pharmacokinetics from microdose and microtracer studies to project clinical-dose profiles with high accuracy. For intravenous administration, the prediction error for clearance and volume of distribution is within a factor of 2. For oral administration, appropriate evaluation informed by the Biopharmaceutics Drug Disposition Classification System (BDDCS) is feasible. They support drug development from early stages through proof of concept (POC) by designing studies in accordance with international standards (FDA, ICH) and by leveraging advanced facilities, including Accelerator Mass Spectrometry (AMS).

Diverse species and disease models

They conduct studies in a wide range of species, including rats, mice, dogs, nonhuman primates (NHPs), and miniature pigs, and maintain a broad portfolio of disease models across therapeutic areas such as oncology, metabolic disease, and neurological disease. They select appropriate models to support drug discovery research and conduct safety and pharmacology studies in compliance with GLP regulations to improve the efficiency of the discovery cycle.

Quality control in accordance with international standards

In addition to a GLP testing framework, it maintains ISO 9001 (certified 2004) and ISO 13485 (upgraded 2016) and enforces quality assurance aligned with investigational drug GMP and GCP requirements. They have established data-integrity (DI)–compliant LC-MS/MS measurements and a stable supply system for radiolabeled compounds. The Drug Discovery Support Center has received PMDA conformity assessment and provides robust support for preparing application data for regulatory authorities in Japan and overseas.

Reference source: Sekisui Medical official websitehttps://www.sekisuimedical.jp/business/adme_tox/about.html

Partner CROs (collaborations with Sekisui Medical)

Bozo Research Center Inc.

Founded in 1972, Bozo Research Center conducts a broad range of contracted nonclinical studies from discovery through the clinical development interface, with a primary focus on pharmacology and safety studies. As a domestic nonclinical CRO, Bozo performs studies using multiple species—mice, rats, guinea pigs, hamsters, rabbits, dogs, nonhuman primates (NHPs), and miniature pigs—as well as various cell-based systems.

Examples of Non-clinical Studies by Sekisui Medical

No case studies are currently listed on the official website.

Corporate Information —Sekisui Medical

Sekisui Medical operates the diagnostic testing business, the pharmaceutical and enzyme business, and the drug discovery support business. The company also manufactures and sells in vitro diagnostic products, provides contract manufacturing of enzymes for biopharmaceuticals, and supports new drug development.By delivering high-quality products and services that meet the needs of the healthcare industry, Sekisui Medical helps advance healthcare.

Address Urbannet Nihonbashi 2-chome Building, 2-1-3 Nihonbashi, Chuo-ku, Tokyo, Japan
Tel 03-3272-0671
Website https://www.sekisuimedical.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