A site where you can find recommended contractors for non-clinical testing|effical " Non-Clinical CROs and Agencies " Biotoxtech Co.,Ltd.

Biotoxtech Co.,Ltd.

Table of Contents
Table of Contents

Biotoxtech Co.,Ltd. is a Korean CRO(contract research organization) specializing in safety studies. The company conducts GLP-compliant non-clinical studies covering toxicity, efficacy, and pharmacokinetics. Biotoxtech operates as a direct research partner, providing contract research services without intermediaries or agents.

Features of Biotoxtech Co.,Ltd.’s Non-Clinical Testing Services

Efficacy evaluation services for disease-specific in vitro and in vivo models

Biotoxtech Co.,Ltd. has established both in vitro and in vivo models for efficacy evaluation across a wide range of disease areas, including diabetes, hypertension, dementia, osteoporosis, and liver disease.
In addition to pharmaceuticals, the company supports the acquisition of various data required for functional evaluation and regulatory approval of health foods and cosmetics.

Biotoxtech Co.,Ltd. is well-versed not only in Korean regulations but also in international guidelines and global research trends, maintaining a comprehensive non-clinical evaluation system to meet diverse client needs.

Support for juvenile animal model studies in pediatric drug development

Another distinctive feature of Biotoxtech Co.,Ltd. is its capability to conduct non-clinical safety studies using juvenile animal models.
For the evaluation of growth, development, motor activity, cognition, and toxicokinetics in pediatric drug development, the company have various established study protocols, which are corresponding to human developmental stages from birth to over 21 days of age.

Their ability to accurately capture the unique physiological responses of pediatric populations—distinct from those of adults—is one of Biotoxtech Co.,Ltd.’s key strengths.

Extensive GLP certifications and proven track record in Korea

Biotoxtech Co.,Ltd. has obtained multiple GLP certifications from Korean authorities, including the Ministry of Food and Drug Safety, the National Institute of Environmental Research, and the Rural Development Administration.
With extensive experience in toxicology, pharmacology, and metabolic studies, Biotoxtech is a highly reliable partner for companies seeking robust, reproducible non-clinical data.

Example of Biotoxtech Co.,Ltd.’s Disease Models

Diabetes model (in vitro / in vivo evaluation models for diabetes)

Biotoxtech has developed in vitro and in vivo preclinical models for diabetes, enabling comprehensive evaluation of candidate compounds through analyses of glucose regulation mechanism, insulin sensitivity, and improvements in glucose metabolism.

In addition to diabetes, the company also offers multiple experimental models and disease progression models that generate high-quality, reliable data for pharmaceutical drugs and functional materials.

Reference: Biotoxtech Co.,Ltd.( http://jpn.biotoxtech.com/pageLink.do?baseMenuNo=9910000&menuNo=9912100)

Biotoxtech Co.,Ltd. Non-Clinical Case Study

PK/TK Combined Pharmacokinetic and Toxicokinetic Study (Simultaneous Evaluation of Efficacy and Safety)

This integrated study evaluates the absorption, distribution, metabolism, and excretion (PK) of drug candidates, as well as the kinetics of toxicity onset (TK).
By analyzing both toxicity and efficacy with a focus on blood concentration—and utilizing advanced analytical techniques such as HPLC, LC/MS, and LC/MS/MS—Biotoxtech Co.,Ltd., they can deliver precise, reliable, and regulatory-compliant data.

Reference: Biotoxtech Co.,Ltd.( http://jpn.biotoxtech.com/pageLink.do?baseMenuNo=9910000&menuNo=9913100)

Biotoxtech Co.,Ltd. Company Information

Address53, Yeongyudanji-ro, Yanggok-eup, Cheongwon-gun, Cheongju-si, Chungcheongbuk-do, Korea
Tel+82 43-210-7777
Websitehttp://jpn.biotoxtech.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, 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