Preclinical CRO Services

Laboratory Sciences

Biomedical Research Support

We provide laboratory-based support for preclinical research, including target validation, assay development and in vitro studies. Our work focuses on generating reliable data through standardised methods and GLP-aligned protocols, supporting translational research and regulatory requirements.

Core R&D Services

Target Discovery & Validation

CRISPR/Cas9 gene editing (knockout/knock-in models)

Biomarker development and multi-omics profiling

Preclinical Pharmacology

In vitro and in vivo efficacy studies

Disease models (rodent and large animal)

PK/PD studies

Translational Research

Biomarker translation and assay development

GLP toxicology and safety studies (IND/CTA support)

Why Collaborate with HuaTeng Biotechnology?

✅ Clinically Relevant Models
Strong capability in both small- and large-animal platforms, including translational large-animal studies.
✅ Integrated Preclinical Platform
From disease modelling to PK/PD, imaging and pathology, delivered through a single workflow.
✅ Global Development Support
GLP-compliant studies aligned with international regulatory requirements.

Let’s Discuss Your Project

We would be happy to explore how we can support your preclinical development programme.

Histology Services

HuaTeng Biotechnology delivers end-to-end histology services to support drug development, disease research, and clinical diagnostics. Our ISO 17025-certified labs, FDA-GLP compliance, and cutting-edge digital pathology platforms ensure high-resolution, reproducible results for global academic, pharmaceutical, and clinical partners.

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In Vivo

At HuaTeng Biotechnology, we deliver end-to-end in vivo research services designed to meet the highest ethical and scientific standards. Our AAALAC-accredited facilities, FDA-GLP compliance, and decades of expertise ensure robust, reproducible outcomes for drug discovery, disease modeling, and therapeutic validation.

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In Vitro

HuaTeng Biotechnology provides comprehensive in vitro research services to drive breakthroughs in drug discovery, biotechnology, and disease mechanism studies. Our ISO 17025-certified labs, cutting-edge technologies, and GLP-compliant workflows ensure high-quality, reproducible data for global clients.

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Why Choose HuaTeng Biotechnology for GLP-Compliant Testing?

Trusted Quality. Global Compliance. Proven Execution.

Global Compliance: AAALAC-accredited facilities with IACUC oversight, aligned with EU Directive 2010/63/EU and USDA standards—ensuring full regulatory acceptance across major markets.

Advanced Imaging Capabilities: Integrated platforms including DSA, IVUS, angiography and micro-CT, enabling real-time evaluation of device performance and in vivo outcomes.

Custom Model Development: Species-specific animal models tailored to complex disease conditions, improving translational relevance and clinical predictability.

Integrated Histopathology Suite: SEM and TEM analysis supported by GLP-grade reporting, enabling seamless submission to PMDA, CE Mark and global regulatory authorities.

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Custom Hotline

+86 15217198166


Email

ht@htscience.com

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