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April 7-11, 2025 New Orleans, LA Booth #41 Each year WRIB program provides you with novel case studies and emerging approaches because it is the only program built on White Paper r...
April 10-11, 2025 Gaithersburg, MD In-person Join Inotiv’s experts for a complimentary, educational workshop to gain in-depth knowledge of Genetic Toxicology.
April 25-30, 2025 Chicago, IL Booth #2509 The AACR Annual Meeting program covers the latest discoveries across the spectrum of cancer research—from population science and preventio...
February 05, 2025 Enhanced liquidity by $27.5 million through the issuance of ...
January 22, 2025 WEST LAFAYETTE, Ind., Jan. 22, 2025 (GLOBE NEWSWIRE) -- Inotiv, Inc. (NASDAQ: NOTV) (the “Company”, or “Inotiv”),
December 30, 2024 WEST LAFAYETTE, Ind., Dec. 30, 2024 (GLOBE NEWSWIRE) -- Inotiv, Inc. (Nasdaq: NOTV) (the “Company”), a leading contract research organization...
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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