Pharma ADMET Testing Market 2025-2034: Key Highlights, Growth Dynamics, and Emerging Trends
2025 Market Reports Update: Market Size Forecasts to 2034, Key Trends, Leading Players, and Top Regions – Get Ahead of the Competition Today!
What Are the Primary Drivers Supporting the Market Growth of thePharma ADMET Testing Market?
The pharma ADMET testing market is gaining traction due to an increase in product approvals. This term primarily involves the authorization process, where bodies like the U.S. Food and Drug Administration (FDA) or the European Medicines Agency (EMA) provide consent for a product to be sold and marketed. ADMET testing, which is vital for verifying the safety and effectiveness of innovative products, is compulsory for such regulatory approvals. For instance, it was reported by the National Library of Medicine, a national health professional resource and a biomedical library based in the U.S, that the FDA approved 55 new drugs in 2023, a substantial increase from 37 approvals in 2022. Thus, the escalating quantity of product approvals propels the growth of the pharma ADMET testing market.
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What is the Predicted Annual Growth Rate of thePharma ADMET Testing Market Impact Industry Trends by 2034?
The market size for pharma ADMET testing has seen a significant increase in the past few years. It’s predicted to climb from $9.67 billion in 2024 to $10.73 billion in 2025, with a compound annual growth rate (CAGR) of 10.9%. The expansion in the historical period can be credited to factors such as the growth in the biopharmaceuticals and biosimilars industry, increased drugs development activities, rising awareness about drug safety, globalisation of clinical trials, and a shift towards in silico modeling.
The market for ADMET testing in the pharmaceutical sector is predicted to experience substantial expansion in the upcoming years. By 2029, it is expected to reach a market size of $17.1 billion, with a CAGR of 12.4%. This projected growth can be associated with factors such as environmental toxicology, safety assessment, pharmacogenomics awareness, the shift towards precision medicine, the rise of biologics and biosimilars, the integration of AI, increased regulatory requirements, and the growth in development of orphan drugs. The forecast period will also witness major trends, including a boost in research partnerships, swift technological progress, advancements in analytical technologies, constant drug safety monitoring, and considerations regarding environmental impacts.
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What Are the Latest Innovations Influencing thePharma ADMET Testing Market?
A leading trend in the pharmaceutical ADMET testing market is the emergence of innovative products. Leading companies in the sector are developing pioneering products like Logica to maintain their competitiveness. For instance, Charles River Laboratories International Inc., a pharmaceutical company from the United States, and Valo Health Inc., a US-based AI-health solutions company, jointly launched an AI-based drug development solution, Logica, in April 2022. This latest solution exploits Valo’s AI-supported Opal Computational Platform to deliver ADMET testing services and other drug delivery frameworks. Logica employs the top-tier predictive models, chemical design and synthesis skills, DNA encoded libraries, and in silico high throughput screening available via Valo’s Opal Computational Platform, in conjunction with Charles River’s leading abilities in all areas of discovery optimization. This includes high throughput screening, medicinal chemistry, ADME, biology, pharmacology, and ultimately, safety testing and IND submission.
Who Are the Major Industry Players Accelerating Growth in thePharma ADMET Testing Market?
Major companies operating in the pharma ADMET testing market include Thermo Fisher Scientific Inc., The Merck Group, Laboratory Corporation of America Holdings, IQVIA Inc., PPD ICON plc, Agilent Technologies Inc., Wuxi AppTec Co. Ltd., Catalent Inc., Covance Inc., Charles River Laboratories International Inc., Eurofins Scientific SE, Beckman Coulter Inc., Perkinelmer Inc., Albany Molecular Research Inc., Evotec A.G., CMIC Holdings Co. Ltd., Promega Corporation, Aptuit LLC, Symeres B.V., Biovia Corp., BioIVT LLC, Cyprotex Limited, InSphero AG, Admescope Ltd., Accelrys Inc.
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Which Primary Segments of the Pharma ADMET Testing Market Are Driving Growth and Industry Transformations?
The pharma ADMET testing market covered in this report is segmented –
1) By Testing Type: In Vivo ADMET Testing, In Vitro ADMET Testing, In Silico ADMET Testing
2) By Technology: Cell Culture, High Throughput, Molecular Imaging, OMICS Technology
3) By Application: Systemic Toxicity, Renal Toxicity, Hepatotoxicity, Neurotoxicity, Other Applications
Subsegments:
1) By In Vivo ADMET Testing: Animal Studies, Pharmacokinetics Studies, Toxicology Studies, Biodistribution Studies
2) By In Vitro ADMET Testing: Metabolism Studies, Drug-Drug Interaction Studies, Absorption Studies, Cytotoxicity and Safety Testing
3) By In Silico ADMET Testing: Predictive Modeling and Simulation, Quantitative Structure-Activity Relationship (QSAR) Analysis, Machine Learning Algorithms for ADMET Predictions, Software Tools for ADMET Profiling
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Which Regions Are Key Players in the Growth of the #What Are the Primary Drivers Supporting the Market Growth of thePharma ADMET Testing Market?# Market?
Asia-Pacific was the largest region in the pharma ADMET testing market in 2024. The regions covered in the pharma ADMET testing market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa.
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