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How has the adme toxicology testing market size evolved in recent years?

The market size for ADME toxicology testing has seen a swift expansion in the earlier years. The market, valued at $10.4 billion in 2024, is expected to reach $11.53 billion in 2025, mounting at a compound annual growth rate (CAGR) of 10.8%. The historical growth can be accredited to strict regulatory norms, emerging drug development undertakings, mounting concerns related to drug safety, advancements in the sector of in vitro testing procedures, and a rise in the outsourcing of toxicology research.

What are the predictions for the adme toxicology testing market size in the coming years?

Over the next few years, the ADME toxicology testing market is projected to experience a swift expansion. The market’s growth rate is anticipated to reach $18.06 billion by 2029, with a compound annual growth rate (CAGR) of 11.9%. The growth during this period is attributable to factors such as the rapid progression of biopharmaceuticals, increasing focus on individualized medicine, advent of state-of-the-art therapies, improved predictive toxicology models, and a worldwide rise in chemical safety testing. Biomarker application expansion, multi-omics data integration, regulatory focus on in vitro testing, collaborations and partnerships, as well as steady technological advancements mark the key trends for the forecast period.

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What key factors are fueling the growth of the adme toxicology testing market?

The surge in the need for innovative drugs is anticipated to fuel the expansion of the ADME toxicology testing market in the future. Innovative drugs refer to therapeutic substances that have not been previously authorized or utilized for treatment. ADME toxicity tests are a critical part of drug development, ensuring that the innovative drug is safe and does not generate any harmful toxins in the body. For example, as per the New Drug Therapy Approvals 2023 report issued by the Center for Drug Evaluation and Research (CDER), a US-based division of the U.S. Food and Drug Administration (FDA), in January 2024, CDER green-lighted 55 innovative drugs in 2023, among which 20 (36%) were identified as first-in-class, as compared to 37 innovative drug approvals in 2022. Hence, the escalating demand for innovative drugs is stimulating the expansion of the ADME toxicology testing market.

How is the global adme toxicology testing market divided into key segments?

The ADME toxicology testing market covered in this report is segmented –

1) By Product Type: Instruments, Software Solutions, Assays Systems, Reagents, Other Products

2) By Method: Cellular Assay, Biochemical Assay, In Silica, Ex-Vivo

3) By Technology: Cell Culture, High Throughput, Molecular Imaging, OMICS Technology, Other Technologies

4) By Application: Systemic Toxicity, Renal Toxicity, Hepatotoxicity, Neurotoxicity, Other Applications

5) By End-User: Cosmetics And Household Products, Pharmaceutical Industry, Animal Industry, Food Industry, Other End Users

Subsegments:

1) By Instruments: High-Throughput Screening Instruments, LC-MS Or MS (Liquid Chromatography-Mass Spectrometry), HPLC (High-Performance Liquid Chromatography), Automated Workstations

2) By Software Solutions: Data Management Software, Simulation And Modeling Software, Risk Assessment Software

3) By Assay Systems: Cell-Based Assays, In Vitro Assays, Bioanalytical Assays

4) By Reagents: Biochemicals, Buffer Solutions, Culture Media

5) By Other Products: Kits And Consumables, Analytical Standards

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Who are the key firms paving the way for growth in the adme toxicology testing market?

Major companies operating in the ADME toxicology testing market include AbbVie Inc., Thermo Fisher Scientific Inc., Boehringer Ingelheim GmbH, Laboratory Corporation of America Holdings, Corning Incorporated, Eurofins Scientific SE, Agilent Technologies Inc., Lonza Group AG, Dassault Systèmes SE, Catalent Inc., Charles River Laboratories International Inc., Beckman Coulter Inc., PerkinElmer Inc., Bio-Rad Laboratories Inc., Curia Global Inc, Promega Corporation, Takara Bio Inc, AB Sciex LLC, QPS Holdings LLC, Simulations Plus Inc., Cyprotex, XenoTech LLC, BioIVT LLC, Absorption Systems, Creative Bioarray, SOLVO Biotechnology Rt., Creative Biolabs Inc, Gentronix Limited, Admecell Inc., Molecular Discovery Ltd.

Which trends are expected to transform the adme toxicology testing market?

Rapid advancements in technology are a prominent developing trend in the ADME toxicology testing sector. Dominant firms within this market are rolling out modern assay solutions rooted in sophisticated technologies like Logica to maintain their market standing. For example, Charles River Laboratories International Inc., an American pharmaceutical firm, in collaboration with Valo Health Inc., which specializes in AI-health solutions from the U.S., inaugurated Logica, a solution for drug development based on AI, in April 2022. This cutting-edge solution applies Valo’s AI-driven Opal Computational Platform for offering ADME toxicology testing services and assorted drug delivery solutions to its users.

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What regions are contributing significantly to the growth of the adme toxicology testing market?

North America was the largest region in the ADME toxicology testing market in 2024. Asia-Pacific is expected to be the fastest-growing region in the forecast period. The regions covered in the ADME toxicology testing market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa.

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