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QUANTIFY ANY PROTEIN, IN ANY SAMPLE, WITH ANY MODIFICATION, WITHOUT ANTIBODIES

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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Reduce costs with our complimentary sample for evaluation in your lab.

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BIOTHERAPEUTIC DEVELOPMENT

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COUNT ON OUR EXPERTISE IN IBD ANIMAL MODELS FOR YOUR NEXT IN VIVO STUDY

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SAMPLE OUR NEW BIOSECURE PLUS™ SOPF MODELS

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FUEL AND TEKLAD DIETS RAW MATERIAL SURCHARGE:

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In Vivo Services In Vivo Services From discovery pharmacology and toxicology,
through regulated enabling safety assessment studies, our team has the in vivo
and analytical capabilities to deliver a variety of flexible solutions adaptable
to your needs. Histology Histology Our industry-leading histology laboratories
support your discovery and nonclinical development projects with a wide range of
services. From tissue processing to digital analysis, our team delivers the
quality you expect.   Pathology Pathology Access our world-class anatomical,
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selection, our in vitro, in vivo, and bioanalytical teams offer the
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analyze, answer, and advance.  Consulting Consulting Our experts deliver the
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biomarker analysis, or bioequivalence studies. Research Models Research Models
Paired with the most comprehensive range of research models in the industry, we
offer the experience, quality, and consistency that is essential to your
success.  Research Model Services Research Model Services Our research model
services group provides high-quality support services worldwide, including
genetically engineered models and services (GEMS), contract breeding services,
surgical services, and more. Teklad Diet and Bedding Teklad Diet and Bedding
What comes out of your research depends in large part on what goes into your
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Program

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NEEDS



SCIENTIFIC POSTER

COMPARATIVE EVALUATION OF DIFFERENT PLATING METHODOLOGIES AND SOURCES OF INDUCED
S9 METABOLIC ACTIVATION ON THE MUTAGENIC POTENTIAL OF N-NITROSODIPROPYLAMINE
USING THE AMES TEST

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.

All Insights


ORTHOPEDIC RESEARCH SOCIETY (ORS)

February 2-6, 2024 Long Beach, CA Booth #17 We look forward to welcoming you to
Long Beach, CA, for the ORS 2024 Annual Meeting, where we will celebra...


SOCIETY OF TOXICOLOGY (SOT)

March 10-14, 2024 Salt Lake City, UT Booth #917 Join Inotiv scientists at SOT
held March 10-14, 2024, at the Salt Palace Convention Center in Salt Lak...

All Events


INOTIV REPORTS FOURTH QUARTER AND FULL YEAR FINANCIAL RESULTS FOR FISCAL 2023
AND PROVIDES BUSINESS UPDATE

December 11, 2023 — Fiscal year 2023 revenue up 4.5% to $572.4 millio...


INOTIV, INC. ANNOUNCES PLAN TO INSOURCE NORTH AMERICAN TRANSPORTATION OPERATIONS

December 6, 2023 WEST LAFAYETTE, Ind., Dec. 06, 2023 (GLOBE NEWSWIRE) -- Inotiv,
Inc. (Nasdaq: NOTV) (the “Company”), a...


INOTIV, INC. TO REPORT FISCAL 2023 FOURTH QUARTER AND FULL YEAR RESULTS AND HOST
CONFERENCE CALL ON MONDAY, DECEMBER 11, 2023

WEST LAFAYETTE, IN - November 27, 2023 -- Inotiv, Inc. (NASDAQ: NOTV) (the
“Company”, “We”, “Our” or “Inotiv”), a leading contract research organization
specializing in nonclinical and analyti...

All News

ON-DEMAND WEBINAR

NOT ALL IBD MODELS ARE CREATED EQUALLY

How Differences Between Experimental IBD Models Can Impact Your Drug Development
Program

SPEAK TO AN EXPERT

UTILIZE OUR EXPERTISE IN DART AND JUVENILE ANIMAL STUDIES (JAS) TO MEET YOUR
NEEDS



SCIENTIFIC POSTER

COMPARATIVE EVALUATION OF DIFFERENT PLATING METHODOLOGIES AND SOURCES OF INDUCED
S9 METABOLIC ACTIVATION ON THE MUTAGENIC POTENTIAL OF N-NITROSODIPROPYLAMINE
USING THE AMES TEST

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.

All Insights


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