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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 7-11, 2024 Baltimore, MD Booth #830 Join the Inotiv team at the American Society of Gene and Cell Therapy’s (ASGCT) annual meeting, the premier ev...
June 3-6, 2024 San Diego, CA The BIO International Convention is the largest and most comprehensive event for biotechnology, representing the full ecosys...
June 10-13, 2024 Rotterdam, Netherlands Booth #72 EACR 2024 is a four day congress dedicated to basic, preclinical, and translational cancer research ...
May 23, 2024 WEST LAFAYETTE, Ind., May 23, 2024 (GLOBE NEWSWIRE) -- Inotiv, Inc. (Nasdaq: NOTV) (the “Company”)
May 15, 2024 — Second quarter fiscal 2024 revenue down 21.5% to $119.0 million
May 14, 2024 WEST LAFAYETTE, Ind., May 14, 2024 (GLOBE NEWSWIRE) -- Inotiv, Inc. (NASDAQ: NOTV) (the “Company”, or “Inotiv”),&nb...
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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