CRO Services

Learn more

下颌骨缺损模型手术中.JPG体外检测中心.jpg

Preclinical Drug Development Solutions

Efficacy & Safety Evaluation for Medical Devices

Learn More

Preclinical R&D for Drug 

Medical Device Testing In Vivo

Learn More

Laboratory Sciences

Biomedical Research Support

dsa.png

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

Preclinical Pharmacology

Translational Research

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


Biomarker development and multi-omics profiling

In vitro and in vivo efficacy studies


Disease models (rodent and large animal)


PK/PD studies

Biomarker translation and assay development


GLP toxicology and safety studies (IND/CTA support)


Why Choose HuaTeng Biotechnology for GLP-Compliant Testing?


Trusted Quality. Global Compliance. Proven Execution.

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.

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.

Leave your information and we will contact you.

华腾英文logo (白).png

Copyright ©️ 2022, NetEase Zhuyou(and its affiliates as applicable). All Rights Reserved.

Our Locations

Quick Links

Our Services

Follow us

Building 11-12, Block B, Lian Dong U Valley, No.29, Bishan Street, Huangpu District, Guangzhou China


Room 503, 5/F Hang Seng Castle Peak Road Building 339 Castle Peak Road Cheung Sha Wan Hong Kong

Home

LinkedIn

Preclinical Drug Development Solutions

Facebook

Twitter

Medical Device Testing In Vivo

Laboratory Sciences

phone
Email