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Target Sufficiency® enables direct, quantitative analysis of drug target systems in cells, biofluids, tissues, and tissue models, including formalin-fixed, paraffin-embedded (FFPE) tissues.
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Inotiv delivers a broad array of nonclinical and analytical services from discovery through clinical development.
Inotiv provides the broadest range of research models and related services to pharmaceutical and biotech companies, government, academia, and other life science organizations.
May 21, 2024 11:30am EDT Hosted Online Drug Discovery is the foundation of the Pharma and Biotech effort to search for novel therapeutics that are safe and treat life-altering dise...
May 22, 2024 Brisbane, CA Join Inotiv’s Genetic Toxicology experts for an informative seminar on resolving unanticipated genetic toxicity results. S
May 23, 2024 San Diego, CA Join Inotiv’s Genetic Toxicology experts for an informative seminar on resolving unanticipated genetic toxicity results. Space is limited! This semin...
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May 14, 2024 WEST LAFAYETTE, Ind., May 14, 2024 (GLOBE NEWSWIRE) -- Inotiv, Inc. (NASDAQ: NOTV) (the “Company”, or “Inotiv”),&nb...
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How Differences Between Experimental IBD Models Can Impact Your Drug Development Program
Due to the current FDA concern and guidance on reducing the risk of Nitrosamine impurities in human drugs, there has been an increased industry need for testing of these impurities using the Bacterial Reverse Mutation (Ames) test. As Nitrosamines are not readily detectable by standard Ames methodologies, specifically cited in the Ames testing guideline (OECD 471), the need for a robust protocol better suited for this class of compounds is warranted.
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