Preclinical Drug Development Solutions

Pharmacodynamic Evaluation

Large Animal Models

Myocardial infarction (pig), diabetes (NHP), stroke (dog), and more.

Small Animal Model

Xenograft tumors, Alzheimer’s (transgenic mice), and inflammation.

Pharmacokinetics & Toxicology (DMPK)

In Vitro Studies

Caco-2 permeability, CYP induction/inhibition, metabolite profiling.

In Vivo ADME

Full PK/PD profiling in rodents, rabbits, and non-human primates.

Toxicokinetics

Dose-range finding and safety margin analysis.

GLP Safety Assessment

Acute/Chronic Toxicity

Genotoxicity, Carcinogenicity

Cardiovascular (hERG) & Respiratory Safety

Biomarker-Driven Risk Mitigation

SPF & Conventional Animal Housing

Imaging & Surgery Suites

Molecular & Pathology Labs

Why Partner with HuaTeng Biotechnology?

Full-Service Expertise: Efficacy, pharmacokinetics (PK/PD), and safety studies under one roof

Globally Accredited Labs: GLP-compliant facilities aligned with OECD, FDA, and NMPA standards

Advanced Infrastructure: SPF-grade animal housing, laminar flow labs, CT/micro-CT imaging, and automated analytics

Species Diversity: Large (NHP, dogs, minipigs) and small (mice, rats) animal models for human-relevant insights

Data-Driven Outcomes: AI-powered analytics and customizable reporting for confident decision-making

Ready to Accelerate Your Program?

Contact us today to discuss your preclinical needs. Our team delivers tailored solutions, transparent timelines, and competitive pricing to keep your pipeline moving forward.

Drug Efficacy Testing in Preclinical Studies

HuaTeng Biotechnology provides comprehensive preclinical efficacy studies to evaluate therapeutic potential, optimize drug candidates, and generate robust data packages for IND submissions. Our customized models bridge the gap between in vitro findings and clinical outcomes.

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ADME/PK Profiling Services

At HuaTeng Biotechnology, we deliver end-to-end ADME/PK profiling services to optimize drug discovery and development, ensuring robust pharmacokinetic and safety data for small molecules, biologics, and novel modalities. Our globally compliant studies bridge preclinical and clinical phases, empowering you to prioritize candidates, mitigate attrition risks, and meet regulatory milestones.

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Non-GLP Toxicology & Safety Pharmacology

HuaTeng Biotechnology provides end-to-end GLP-certified safety & toxicology studies for global clients. Expertise in small (rodent) and large animal models (NHP/canine). OECD, FDA, ICH compliant. Fast-track your drug development.

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Why Choose Huateng Bio for GLP-Compliant Testing?

Global Compliance: AAALAC-accredited facilities with IACUC protocols aligned with EU Directive 2010/63/EU and USDA standards.

Advanced Imaging: DSA, IVUS, angiography, and micro-CT for real-time device performance tracking.

Custom Model Development: Species-specific animal models for complex disease states.

Histopathology Suite: SEM/TEM analysis with GLP-grade reporting for PMDA/CE Mark submissions.

Preclinical Drug Development Solutions