Developing Antibody Drug Conjugate (ADC) therapeutics? Inotiv has mass spectrometry assays to quantify your ADC target protein in any sample type, including FFPE tissue, without antibodies. We have developed assays to 27 ADC targets for oncology and other therapeutic applications.
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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.
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.
June 22-25, 2025 Chicago, IL Booth #101 We’re excited to participate in the STP’s 44th Annual Meeting, centered on the theme: “Toxi...
July 1-3, 2025 | July 8-10, 2025 8:00 AM – 2:00 PM ET Online live sessions We’re excited to announce our participation in the BSTP's
July 17, 2025 11:00 AM – 12:30 PM ET Online webinar The therapeutic promise of RNA depends on effective delivery, with lipid nanoparticles (LNPs) serving as the most widely used ve...
Dale Wright and Brian Bond from Inotiv discuss the importance of taking a holistic approach to glucagon-like peptide-1 re...
May 7, 2025 — Second quarter fiscal 2025 revenue increased 4.4% to $124.3 million — Year-to-date fiscal 2025 revenue de...
April 23, 2025 WEST LAFAYETTE, Ind., April 23, 2025 (GLOBE NEWSWIRE) -- Inotiv, Inc. (NASDAQ: NOTV) (the “Company”, or “Inotiv”...
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.
June 22-25, 2025 Chicago, IL Booth #101 We’re excited to participate in the STP’s 44th Annual Meeting, centered on the theme: “Toxi...
July 1-3, 2025 | July 8-10, 2025 8:00 AM – 2:00 PM ET Online live sessions We’re excited to announce our participation in the BSTP's
July 17, 2025 11:00 AM – 12:30 PM ET Online webinar The therapeutic promise of RNA depends on effective delivery, with lipid nanoparticles (LNPs) serving as the most widely used ve...
Dale Wright and Brian Bond from Inotiv discuss the importance of taking a holistic approach to glucagon-like peptide-1 re...
May 7, 2025 — Second quarter fiscal 2025 revenue increased 4.4% to $124.3 million — Year-to-date fiscal 2025 revenue de...
April 23, 2025 WEST LAFAYETTE, Ind., April 23, 2025 (GLOBE NEWSWIRE) -- Inotiv, Inc. (NASDAQ: NOTV) (the “Company”, or “Inotiv”...
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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