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Toxicology

Rigorously assess toxicology to ensure the safety of your drug discovery programs

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Integrated Drug Discovery
Target Validation
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Focused screen
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Process Research & Development (PR&D)
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Analytical Chemistry
ADMET & DMPK
In vitro ADME Assays
Bioanalysis
In vivo PK Screen
Toxicology
Cardiotoxicity
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Hepatotoxicity
Neurotoxicity
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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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Precision ADME & DMPK insights for Drug Discovery

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Developed and validated LC-MS/MS assays for T4 and Thyroxin to study in vitro UGT induction in rat and human hepatocytes."

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