Preclinical toxicology studies should reliably assess the safety of new drug entities, thus building a multi-faceted understanding of compounds to lay the groundwork for clinical trials and regulatory approval.
TORONTO, Oct. 14, 2021 /PRNewswire-PRWeb/ -- Well-designed and meticulously implemented preclinical toxicology studies are crucial for the success of any drug development program. Preclinical toxicology studies should reliably assess the safety of new drug entities, thus building a multi-faceted understanding of compounds to lay the groundwork for clinical trials and regulatory approval. At times, preclinical studies may lead to the attrition of compounds during preclinical development or the Good Laboratory Practices (GLP) toxicology phase; this helps save millions of dollars during the drug development program.
In this webinar, our featured speaker will present a roadmap that seamlessly integrates the various preclinical studies, thus accelerating the initiation of clinical trials. The roadmap covers various aspects of the preclinical journey, developing a tox-suitable formulation, running the dose range finding (DRF) to set the doses for GLP toxicology and the full scale of GLP tox studies.
Register for this webinar to learn about the best way to plan for investigational new drug (IND)-enabling preclinical toxicology studies.
For more information, or to register for this event, visit A Practical Roadmap for IND-Enabling Safety and Toxicology Studies.
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