Preclinical Drug Development Solutions
Efficacy & Safety Evaluation for Medical Devices
Preclinical R&D for Drug
Medical Device Testing In Vivo
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
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.
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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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Preclinical Drug Development Solutions
Medical Device Testing In Vivo
Laboratory Sciences