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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 ...
Company reaffirms commitment to maintaining appropriate standards of animal welfare June 3, 2024 WEST LAFAYETTE, Ind., June 03, 2024 (GLOBE NEWSWIRE) -- Inotiv Inc. – ...
June 3, 2024 In May 2022, as previously reported and as part of a federal investigation, federal authorities conducted a search at the canine breeding facility in Cumberland Co...
May 23, 2024 WEST LAFAYETTE, Ind., May 23, 2024 (GLOBE NEWSWIRE) -- Inotiv, Inc. (Nasdaq: NOTV) (the “Company”)
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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