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info@huatengbiotech.com

WORKING HOURS

Mon, Fri 8.30 - 18.00 GMT+8

Weekend  CLOSED

LOCATION

Guangzhou

Hong Kong

One-Stop Preclinical Research Service: 

From Early Research to Global Submission

Supporting global MedTech and pharmaceutical innovation with reliable models, translational insights, and regulatory-ready data.
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CRO Services

Comprehensive solutions to accelerate your medical research and development

Translational Animal Models for Human Diseases

Preclinical Drug Development Services

- Efficacy studies in disease models

- ADME/PK and bio-distribution analysis

- GLP toxicology and safety assessment

Integrated Preclinical Research Services

Preclinical Evaluation for Medical Devices

- In vivo & in vitro study design and execution

- Histology, pathology and biomarker analysis

- Molecular and cellular biology support

- Customised preclinical research solutions

- Cardiovascular and structural heart devices

- Dermal, wound healing and aesthetic products

- Orthopedic and dental materials

- Hemostasis and biomaterial evaluation

- 300+ validated small & large animal models

- Disease-specific and translationally relevantsystems

- Custom model development aligned withregulatory needs

Platforms

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WHY CHOOSE US

Efficient, Compliant and Excellent

2000+

300+

20000㎡

3000+

Global Partners

Successful

Registration Cases

Laboratory Space

CRO Projects

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About HuaTeng

HuaTeng Biotechnology: Advancing Your Path from Discovery to Clinic

At HuaTeng Biotechnology, we go beyond generating data — we deliver reliable, decision-ready results to support your therapeutic and diagnostic development.


We understand that successful development depends on the translational relevance of preclinical models and the quality of data submitted to global regulators. By combining clinically relevant disease models with our AAALAC-accredited and GLP-compliant platform, we help improve study reliability and accelerate R&D timelines.


Whether supporting IND-enabling studies for novel drugs or conducting preclinical evaluation for Class III medical devices, our team ensures studies are executed with consistency, scientific rigor, and regulatory awareness.



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With experience from over 3,000 CRO projects and support for 300+ regulatory submissions, we provide proven capabilities to advance your programs with confidence.

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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

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