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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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September 8-11, 2024 Copenhagen, Denmark Booth #15 EUROTOX is the Federation of European Toxicologists and European Societies of Toxicology, which tog...
September 11, 2024 11 am—12 pm Online webinar Protect your research with robust rodent health monitoring. Ensuring the health and well-being of your rodent research colony...
September 15-18, 2024 Honolulu, HI Booth #108 This co-organized meeting for JSSX and ISSX with a focus on The Future of Translational Xenobiotic Resea...
September 6, 2024 Inotiv is pleased to announce that our Talent Acquisition team has been selected as one of ...
August 28, 2024 WEST LAFAYETTE, Ind., Aug. 28, 2024 (GLOBE NEWSWIRE) -- Inotiv, Inc. (Nasdaq: NOTV), a lead...
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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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