Huaten Bio delivers globally accredited preclinical toxicology services to de-risk your drug, chemical, or medical device development. Our AAALAC-accredited facilities support small animal models (rodents, rabbits) and large animal studies (non-human primates, canines, swine) under strict GLP compliance.
| Core Services |
|---|
| Acute/Subacute Toxicity Testing (Single & Repeat Dose) |
| Genotoxicity & Carcinogenicity Studies (Ames Test, Micronucleus) |
| Reproductive Toxicology (Segment I-III, Developmental & Fertility Assessments) |
| Safety Pharmacology (Cardiovascular, Respiratory, CNS) |
| Customized Study Design (Dose-Ranging, ADME/PK Integration) |
| Dual-Capacity Facilities | Global Compliance Expertise | Speed-to-Market Advantage |
|---|---|---|
| Dedicated SPF zones for rodents | AAALAC-certified NHP/dog housing | Full alignment with OECD 423/452, ICH S1-S12, FDA Redbook | 30% faster study initiation vs. industry average |
| Surgical suites & advanced imaging (PET/CT, MRI) | Audit-ready data packages for EMA/FDA/PMDA submissions | Real-time biometrics dashboards for milestone tracking |
Rat
Mouse
Rabbit
Mini-pig
Beagle Dog
Cynomolgus/NHP
Telemetry-based cardiovascular monitoring
Flow cytometry for immunotoxicity profiling
Digital histopathology (Whole Slide Imaging)
Q: Do you support combo product testing (drug-device)?
A: Yes. Our team specializes in integrated medical device/drug toxicity assessments per ISO 10993-1 and ICH guidelines.
Q: What's the lead time for acute oral toxicity (OECD 423)?
A: Standard reports delivered in 8-10 weeks, including hematology/biochemistry analysis.