Inotiv’s team of experts provide the guidance needed to help navigate your molecule through the non-regulated and regulated preclinical stages of drug development and beyond. We offer a comprehensive array of safety assessment services, using multiple species and routes of administration, to help you achieve your development milestones and goals. With a focus on quality and data integrity, we deliver a scientifically sound, high quality, on-time product for your regulatory submissions.

Take advantage of our long and impeccable regulatory history, world-class team of scientists, and track record of providing attentive, decisive service. For your in vivo, toxicology, histopathology, and DMPK/bioanalysis services, expect more attention, more insight, and a superlative experience as we deliver the right-size solutions essential to your success.

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