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Toxicology
Rigorously assess toxicology to ensure the safety of your drug discovery programs
Preclinical toxicology studies are an essential part of drug development, identifying any adverse effects on living organisms. They help to evaluate the potential safety and toxicity of a drug candidate before it is tested in human clinical trials.
Our toxicology studies are powered by a multidisciplinary team of scientists and study directors conducting programs under GxP regulations. This ensures our results and interpretation meets the exacting standards required for approval:
- Our team has a strong mechanistic understanding of toxicology, and can help you efficiently determine potential risk factors early in the drug development of your therapeutic
- We can provide tailored non-GLP toxicology studies making it possible for you to make faster data-driven decisions for your IND-enabling programs
These studies play a pivotal role in identifying the appropriate dose range for a drug candidate and can provide information about potential side effects and adverse reactions. Preclinical toxicology studies help determine the potential risks and benefits of a drug candidate and can provide a basis for regulatory approval.
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