Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » JOINN Laboratories (China) Co., Ltd.

JOINN Laboratories (China) Co., Ltd.

JOINN Laboratories (China) Co., Ltd. is a leading China-based global contract research organization (CRO) providing integrated non-clinical research services across its own facilities. The company offers end-to-end support ranging from non-clinical studies, safety assessment, and disease model development to IND-enabling and regulatory submission support.
This section outlines the key features of JOINN Laboratories (China) Co., Ltd.’ non-clinical services, examples of disease models, and available case information.

Features of JOINN Laboratories (China) Co., Ltd.’ Contract Services for Non-Clinical Studies

High-quality material manufacturing using GMP-compliant bioreactor facilities

JOINN Laboratories (China) Co., Ltd. provides high-quality material manufacturing services utilizing GMP (Good Manufacturing Practice)-compliant bioreactor systems.Upstream processing capabilities include stainless steel bioreactors with volumes of up to 1,000 L, as well as single-use bioreactors with capacities of up to 500 L, enabling flexible optimization of cell culture processes.
These facilities support the production of preclinical materials as well as biologics and antibody therapeutics intended for clinical development, allowing JOINN to accommodate a wide range of client development needs. In combination with integrated in-process testing technologies, the company ensures robust process control and generates reliable, high-quality data.

Comprehensive IND registration and submission support

JOINN Laboratories (China) Co., Ltd.comprehensive support for Investigational New Drug (IND) registration and submission,aligned with regulatory requirements across multiple regions, including China (NMPA), the United States (FDA), and Japan (PMDA). Services cover the preparation of regulatory documentation from the non-clinical stage onward, including compilation of pharmacology and toxicology data, as well as development of clinical trial protocols and informed consent documents.
Dedicated regulatory teams develop submission strategies tailored to the specific characteristics of each compound and its development stage, streamlining the regulatory process, reducing time to approval, and enabling clients to efficiently prepare for global clinical trial initiation.

Evaluation systems compliant with international regulatory standards

JOINN Laboratories (China) Co., Ltd. conducts a broad range of safety studies in compliance with international standards, including FDA, ICH, and GLP requirements.Available studies include safety pharmacology, general toxicity, genotoxicity, and pathology assessments, as well as system-specific safety evaluations targeting cardiovascular, respiratory, and central nervous systems.
All studies are performed under standardized quality control systems, generating high-reliability data suitable for regulatory submission. Through comprehensive safety profiling and rigorous risk assessment, JOINN supports informed decision-making from the early stages of drug development.

Examples of Disease Models Available at JOINN Laboratories (China) Co., Ltd.

JOINN Laboratories (China) Co., Ltd. offersmetabolic disease models, including diet-induced obesity (DIO) models and type 2 diabetes models, for the establishment and evaluation of disease-relevant pathophysiology.In DIO models, animals such as mice fed a high-fat diet are used to reproduce human obesity and associated conditions, including insulin resistance and dysregulated lipid metabolism. Disease-related endpoints such as body weight gain, blood glucose fluctuations, and lipid profile changes can be assessed, supporting efficacy and safety evaluation of drug candidates as well as mechanistic studies.

In the field of infectious diseases,JOINN Laboratories (China) Co., Ltd. also providesanimal models, including influenza virus infection models.These models enable evaluation of antiviral efficacy, immune responses, and safety profiles of candidate therapeutics and vaccines in virus-infected animals, generating data that support drug discovery and development for infectious disease treatment and prevention.

JOINN Laboratories (China) Co., Ltd. Non-Clinical Case Study

No public nonclinical case examples are currently disclosed.

JOINN Laboratories (China) Co., Ltd. Company Information

Address No. 5 Jia, Rongjing East Street, Economic and Technological Development Zone, Beijing, China (Beijing Head Office)
Tel +86-10-67869966
Website https://www.joinnlabs.com/en/

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
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and Reviews
Proven Capability, Expertise and Track Record
Top 3 Non-Clinical CRO Services