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市场调查报告书
商品编码
1853399
in vitro安全药理分析的全球市场 (~2035年):产品类型·用途·技术平台·终端用户·各服务供应商Global In Vitro Safety Pharmacology Profiling Market Research Report by Product Type, by Application, by Technology Platform, by End User, and by Service Provider Forecast till 2035 |
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预计体外安全药理学分析市场规模将成长至57.459亿美元,预测期内复合年增长率(CAGR)为8.4%。体外安全药理学分析是一种基于实验室的方法,用于评估新化合物与关键生物标靶的相互作用,并预测不良副作用。这使得研究人员能够透过观察人类体外的细胞反应来确定药物安全性。
得益于人工智慧、机器学习、晶片器官和3D细胞培养等技术的进步,全球体外安全药理学分析市场正在不断发展。预测毒理学正成为早期识别毒性副作用(例如心臟毒性、肝毒性和神经毒性)的关键工具,从而提高决策准确性并减少动物实验的数量。高精度和与人类的相关性是这些方法在现代药物和生物製药开发中变得至关重要的原因。
报告属性详情
北美体外安全性药理学分析市场正经历显着成长,这主要得益于强大的製药基础和对早期毒性检测日益增长的需求。此外,体外测试外包给经验丰富的合约研究组织 (CRO) 的广泛应用,使得即使是中小企业也能在无需大量资本投入的情况下参与先进的安全性研究。2024年,美国和加拿大分别贡献了7.267亿美元和3,990万美元,使北美成为主要市场。
同时,由于监管更加严格以及动物试验的减少,欧洲体外安全药理学分析市场地位逐步巩固。目前,学术机构、合约研究组织(CRO)和产业合作伙伴之间的合作正在进行,推动着整个地区的持续技术创新和新方法的发展。 2024年,英国以2.167亿美元的市场规模领先欧洲市场,其次是德国和法国,分别为1.69亿美元和1.4亿美元。
亚太地区是成长最快的市场之一,这得益于製药业的快速发展和监管力度的加强。 CRO网路的当前和未来扩张正在吸引寻求成本效益和品质的全球公司。到 2024 年,中国和日本的市场规模将分别达到 1.475 亿美元和 1.004 亿美元,进一步巩固其市场地位。
本报告分析了全球体外安全药理学分析市场,并提供了市场定义和概述、影响市场成长的各种因素分析、市场规模趋势和预测、按不同细分市场、地区和主要国家/地区划分的市场细分、竞争格局以及主要公司的简介。
Global In Vitro Safety Pharmacology Profiling Market Research Report by Product Type (Cell-Based Assays, Organ-Based Assays, Tissue-Based Assays), by Application (Cardiotoxicity Profiling, Neurotoxicity Profiling, Hepatotoxicity Profiling, Nephrotoxicity Profiling, Genotoxicity & Carcinogenicity Assays, Others), by Technology Platform (High-Throughput Screening, Multiparametric Flow Cytometry, Microscopy-Based Assays, Patch Clamp Electrophysiology, Others), by End User (Pharmaceutical and Biotechnology Companies, Contract Research Organizations, Academic and Research Institutions), and by Service Provider [In-House Testing (Pharma Companies), Outsourced Testing (CROs & Labs)] Forecast till 2035
Industry Overview
The In Vitro Safety Pharmacology Profiling Market is expected to attain a value of USD 5,745.9 million, registering a CAGR of 8.4% during the forecast period. In vitro safety pharmacology profiling is a laboratory-based approach that assesses how a new compound interacts with key biological targets to predict adverse side effects. It helps researchers determine drug safety by studying cellular responses outside the human body.
Global In Vitro Safety Pharmacology Profiling Market is evolving with the help of such technologies as AI, machine learning, organ-on-a-chip, and 3D cell culture. Predictive toxicology is becoming more and more the tool for toxic side effects identification cardiotoxicity, hepatotoxicicity, and neurotoxicity at the earliest stage, thus improving decision-making and reducing the number of animal tests. The great precision and relevance to humans are the reasons for which these methods have come to be indispensable in modern drug and biologics development.
Major Company Development
Eurofins broadened its worldwide network through a series of acquisitions it made in April 2025. It closed the purchase of SYNLAB's clinical diagnostics operations in Spain, and in July 2024, it acquired Labormar. The latter transaction extended Eurofins' reach in Latin America and elevated its Food, Environmental, Cosmetic, and Pharmacological testing capabilities in Colombia.
Major players in the global in vitro safety pharmacology profiling market are Eurofins, ICE Bioscience, WuXi Biology, Charles River Laboratories, Mediford Corporation, Aurigene, Labcorp, Evotec, Creative Biolabs, and Accelera S.r.l.
Report Attribute Details
Industry Segmentations
The North American in vitro safety pharmacology profiling market has experienced significant growth, which has been facilitated by the region's robust pharmaceutical base and the increasing demand for early toxicity detection. Besides, the practice of outsourcing in vitro testing to skilled CROs has allowed smaller companies to engage in advanced safety research without the necessity of large capital expenditures. The North American market reached significant levels in 2024, with the U.S. contributing USD 726.7 million and Canada USD 39.9 million to regional growth.
It's European market for in vitro safety pharmacology profiling that was able to gradually strengthen its position due to strict regulations and the trend of animal testing abolition. The collaboration between academic institutions, CROs, and industry partners is underway and providing continuous innovations and methods throughout the region. In 2024, Europe's market was led by the UK at USD 216.7 million, while Germany and France posted USD 169.0 million and USD 140.0 million.
The Asia-Pacific region has turned out to be one of the quickest developing markets, which is a result of the fast pharmaceutical growth and the improved regulatory scrutiny. The current and future expansion of the CRO network in the region is welcoming global companies who are in search of the most economically and qualitatively advantageous testing services. Asia-Pacific continued to strengthen its position in 2024, with China and Japan generating USD 147.5 million and USD 100.4 million.
In South America, market growth is supported by rising R&D investments and evolving safety regulations led by ANVISA and INVIMA. In vitro models are helping regional drug developers minimize late-stage failures by identifying adverse reactions earlier. The growing number of CROs offering specialized assays, such as hERG and hepatocyte studies, has improved access to local testing.
The Middle East and Africa are seeing a steady rise in demand for in vitro safety pharmacology profiling as pharmaceutical research expands. In vitro techniques are preferred for their affordability, rapid results, and ethical compliance. With new R&D facilities emerging, countries like the UAE, Saudi Arabia, and South Africa are positioning themselves as regional leaders. Growing collaboration between CROs and academic institutions is helping strengthen safety research.