Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » LSI Medience Corporation

LSI Medience Corporation

Table of Contents
Table of Contents

LSI Medience Corporation is a contract research organization providing GLP-compliant non-clinical studies. These studies are conducted at the LSIM Safety Science Institute, a consolidated subsidiary. Through testing performed within its own group facilities, the company supports the delivery of high-quality data that meets international regulatory standards.

Features of LSI Medience Corporation’s Non-clinical Contract Services

Highly reliable GLP-compliant testing framework

LSIM Safety Science Institute—the subsidiary responsible for non-clinical studies—has obtained multiple GLP certifications, including Pharmaceuticals GLP. The institute is highly regarded by third-party authorities such as Japan’s Ministry of Health, Labour and Welfare, the Ministry of Agriculture, Forestry and Fisheries, the Ministry of the Environment, as well as being recognized as compliant with OECD principles.

Within its in-house facilities, LSI Medience Corporation has established a system capable of conducting world-class safety studies for pharmaceuticals, agrochemicals, and chemical substances.

Comprehensive non-clinical capabilities including toxicology and pharmacokinetics

LSIM Safety Science Institute conducts a broad spectrum of non-clinical studies— toxicity testing (acute, repeated-dose, reproductive and developmental, and genotoxicity) , pharmacokinetics, metabolite identification, and analytical method validation.

A wide range of animal species can be used, including rats, mice, dogs, monkeys, and rabbits. Study designs can be customized to meet various regulatory and submission requirements. The institute supports development not only for pharmaceuticals but also agrochemicals and chemical substances across different development stages.

Strong compliance with global regulations and robust quality documentation

Because LSIM Safety Science Institute adheres to OECD guidelines in addition to Japanese GLP, it is capable of conducting studies intended for international joint development programs and overseas regulatory submissions.

The institute maintains an internal Quality Assurance department that ensures rigorous quality control, including audits and reporting. Study protocols and final reports can also be prepared in English, providing strong support for documentation required by international regulatory agencies.

Examples of Disease Models Available at LSI Medience Corporation

Pathological models for pain and inflammation assessment

As part of their pharmacology testing services, LSIM Safety Science Institute conducts non-clinical studies using various pathological models designed for the evaluation of pain and inflammation.

In their animal models, they analyse the efficacy of anti-inflammatory agents, analgesics, and other candidate compounds. Pharmacological effects—including mechanism of action, dose-response curve, and duration of the effect—are evaluated to support a smooth transition to the next clinical development stages.

Details regarding specific model protocols can be discussed during preliminary consultations.

Reference: LSI Medience Corporation Official Website https://www.ankaken.dmsv.tokyo/test/pharmacology.html

LSI Medience Corporation Non-clinical Case Studies

DMPK characterization support for drug candidate compounds

The official website does not currently provide publicly available case study information.

LSI Medience Corporation Company Information

Address3-30-1 Shimura, Itabashi-ku, Tokyo
Tel03-5994-2111
Websitehttps://www.medience.co.jp/

3 Recommended Contract Research Organizations
for Non-Clinical Studies
— by Target goal and Expertise

In non-clinical development, the choice of contract research organization shapes the quality of the data and the time it takes to reach the next decision. Below, three CROs are introduced by the type of study they support: pharmacology (efficacy) studies, safety studies, and pharmacokinetic (PK/PD) studies. Each summary describes the services the company offers so that you can match a provider to your target and development objective.

Pharmacology (Efficacy) StudiesDisease-Relevant Models for
Translational Drug Evaluation
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/)

SMC Laboratories, Inc.

SMC Laboratories is a specialized non-clinical CRO focused on in vivo pharmacology and efficacy studies using disease-relevant animal models, particularly in fibrosis, inflammation, metabolic diseases, and oncology.

Areas of Expertise
Disease-Relevant Model Portfolio

SMC Laboratories offers models covering the liver, lung, kidney, intestine, and oncology. Its portfolio includes the proprietary STAM™ model for MASH, fibrosis, and hepatocellular carcinoma.

Study Design Based on Target Biology

Study plans are developed around the target biology, mechanism of action, disease stage, and development objective. Pharmacological endpoints can be combined with histopathology, biomarkers, and disease-specific readouts.

Support from Target Validation to Proof of Concept

With experience from more than 1,000 studies for clients in 30 countries, SMC Laboratories supports programs from target validation and candidate selection through in vivo proof-of-concept studies.

Safety StudiesComprehensive Safety Assessment for
Preclinical Development
Charles River Laboratories
Reference: Charles River Laboratories official website (https://www.criver.com/)

Charles River Laboratories

Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.

Areas of Expertise
General Toxicology Across Study Designs

Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.

Non-GLP and GLP Study Support

Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.

Integrated IND-Enabling Safety Assessment

Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.

Pharmacokinetic (PK/PD) StudiesConnecting Drug Exposure with
Pharmacological Response
Inotiv
Reference: Inotiv official website (https://www.inotiv.com/)

Inotiv

Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.

Areas of Expertise
Pharmacokinetic Characterization

PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.

Exposure–Response Evaluation

Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.

Integrated DMPK and Development Support

Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.

By Therapeutic Area
Disease Animal Models
and Reviews
Proven Capability, Expertise and Track Record
Top 3 Non-Clinical CRO Services