Inotiv’s trusted team of experts collaborate with you to provide the guidance needed to help navigate your molecule through the non-regulated and regulated preclinical milestones of drug development. To help you achieve your development goals, we offer a comprehensive suite of safety assessment services, combined with multiple species and routes of administration. Your compound is our priority, and you should expect our focus to be on providing scientifically sound, high-quality data, and on-time delivery that keeps your development program on track.
As your partner, you can leverage our team of world-class scientists with a long and impeccable regulatory history. With their extensive experience and proven track record, you can expect to receive attentive, decisive support throughout your development process. Take advantage of our in vivo safety assessment, toxicology, histopathology, and analytical services to help you progress and develop your pharmaceutical, chemical, or medical device. With Inotiv by your side, expect more attention, more insight, and a superlative experience as we deliver the right-size solution essential to your success.
Inotiv offers a range of general toxicology studies to evaluate the safety of drugs, medical devices, and other chemicals. We design and conduct studies according to international regulations and our toxicology expertise can help assess potential risks and ensure the safety of your product.
Genetic Toxicology Genetic Toxicology Inotiv provides a complete Genetic Toxicology solution, including non-GLP screening, all required in vitro and in vivo regulatory assays and follow-up/secondary testing. Bioanalysis BioanalysisWe offer customized end-to-end bioanalytical solutions to achieve your milestones effectively and on schedule, supporting the development of a wide range of therapeutics from discovery through Phase IV.
Drug Metabolism and Pharmacokinetics (DMPK) Drug Metabolism and Pharmacokinetics (DMPK)From hit-to-lead to lead optimization through candidate selection, our in vitro, in vivo, and bioanalytical teams offer the fit-for-purpose solutions you need at any stage of development to help you analyze, answer, and advance.
Developmental and Reproductive Toxicology (DART) Developmental and Reproductive Toxicology (DART)Inotiv has built an internationally recognized DART and JAS study team through close collaboration with industry-leading experts.
Our nonclinical testing services feature veterinary surgeons, state-of-the-art imaging, and a commitment to excellence to advance your medical device.
Histology HistologyOur industry-leading histology laboratories support your discovery and nonclinical development projects with a wide range of services. From tissue processing to digital analysis, our team delivers the quality you expect.
Pathology Pathology Access world-class anatomical, clinical, and medical device pathology services, from routine histochemistry, IHC, IF, and ISH to stereology. Consulting Consulting Our experts deliver the insights you deserve to get the answers you need, whether in DMPK data analysis, biomarker analysis, or bioequivalence studies. Computational Toxicology Computational ToxicologyInotiv’s computational toxicology group offers you a wide range of expertise across informatics areas, allowing us to draw on data from your assays, in-house resources, and relevant literature to deliver the insights you need.
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