The ADME toxicology testing market is expected to grow at a compound annual growth rate (CAGR) of 11.5% between 2022 and 2030 from its estimated valuation of USD 6.65 billion in 2021. The market is driven by the importance of ADME toxicology testing in drug development, as it enables pharmaceutical companies to evaluate the safety and efficacy of novel drug candidates prior to advancing them to clinical trials and eventual market release.

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GROWTH DRIVERS
Strong demand for ADME toxicity testing is driven by the expanding need for novel pharmaceutical products to meet a broad range of medical uses. The demand for comprehensive ADME testing services is rising as pharmaceutical companies step up their efforts to develop novel drugs. Additionally, there is a growing emphasis on ensuring the safety and efficacy of pharmaceutical products, as these tests are critical in identifying potential side effects early in the drug development process, allowing companies to minimize risks and maximize therapeutic benefits.
The need for novel therapeutics is fueled by the rising prevalence of chronic diseases like cancer, cardiovascular diseases, and neurological conditions. In addition, regulatory requirements enforced by health authorities like the FDA and EMA (European Medicines Agency) require comprehensive ADME toxicology testing as part of the drug approval process.
MARKET SEGMENTATION:
· By Technology –
• Cell culture
• High throughput screening
• Molecular Imaging
• OMICS Technology
· By Application –
• Systematic Toxicity
• Renal Toxicity
• Hepatotoxicity
• Neurotoxicity and others
· By Method Outlook –
• Cellular Assay
• Biochemical Assay
• In-silica
• Ex-vivo
· By Region –
• North America
• Europe
• Asia Pacific
• Middle East and Africa
• South America

Global Key Players:
· Thermo Fisher Scientific
· Promega Corp.
· Agilent Technologies
· Curia Global
· Dassault Systemes
· Beckman Coulter
· Catalent
· Charles River Laboratories
· LabCorp Drug Development
· Eurofins Scientific

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