Toxicology

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.