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Efficacy Evaluation

We strictly adhere to national regulations on laboratory animal welfare and ethics, establishing a comprehensive system for microbial quality control and genetic background verification throughout the entire process. This ensures that every experimental mouse strain we release is genetically pure, healthy, and free of specific pathogens, providing a highly reproducible foundation for your research.

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Efficacy Evaluation

Related Resources

Safety Assessment

I. Service Overview

The objective of preclinical drug toxicology studies is to characterize and identify the toxic effects of a drug, determine the target organs and the relevant dose range, assess whether the toxic effects are reversible, elucidate the underlying mechanisms of toxicity, and conduct a comprehensive and systematic evaluation of the drug’s safety profile, thereby providing critical reference data for clinical trials.
In compliance with GLP standards, we provide clients with a full range of test and study services that meet the requirements of CFDA or ICH guidelines.


II. Service Items

General toxicology experiments:
Acute Toxicity Study: Single-Dose Toxicity Test (Rodents and Non-Rodents)
Long-term toxicity studies: Repeated-dose toxicity studies (rodents and non-rodents)
Special toxicity study:
Local toxicity studies: hemolysis, sensitization, and irritation tests
Genotoxicity assays: chromosome aberration assay, micronucleus assay, Ames test
Reproductive and developmental toxicity study
Carcinogenicity test