Preclinical CRO Services

in vivo

Accelerate Preclinical Research with Ethical, Reliable In Vivo Solutions

At Huateng Biotech, 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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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.

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