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市場調查報告書
商品編碼
1853399
in vitro安全藥理分析的全球市場 (~2035年):產品類型·用途·技術平台·終端用戶·各服務供應商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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預計體外安全藥理學分析市場規模將成長至57.459億美元,預測期內複合年增長率(CAGR)為8.4%。體外安全藥理學分析是一種基於實驗室的方法,用於評估新化合物與關鍵生物標靶的相互作用,並預測不良副作用。這使得研究人員能夠透過觀察人類體外的細胞反應來確定藥物安全性。
得益於人工智慧、機器學習、晶片器官和3D細胞培養等技術的進步,全球體外安全藥理學分析市場正在不斷發展。預測毒理學正成為早期識別毒性副作用(例如心臟毒性、肝毒性和神經毒性)的關鍵工具,從而提高決策準確性並減少動物實驗的數量。高精度和與人類的相關性是這些方法在現代藥物和生物製藥開發中變得至關重要的原因。
報告屬性詳情
北美體外安全性藥理學分析市場正經歷顯著成長,這主要得益於強大的製藥基礎和對早期毒性檢測日益增長的需求。此外,體外測試外包給經驗豐富的合約研究組織 (CRO) 的廣泛應用,使得即使是中小企業也能在無需大量資本投入的情況下參與先進的安全性研究。2024年,美國和加拿大分別貢獻了7.267億美元和3,990萬美元,使北美成為主要市場。
同時,由於監管更加嚴格以及動物試驗的減少,歐洲體外安全藥理學分析市場地位逐步鞏固。目前,學術機構、合約研究組織(CRO)和產業合作夥伴之間的合作正在進行,推動著整個地區的持續技術創新和新方法的發展。 2024年,英國以2.167億美元的市場規模領先歐洲市場,其次是德國和法國,分別為1.69億美元和1.4億美元。
亞太地區是成長最快的市場之一,這得益於製藥業的快速發展和監管力度的加強。 CRO網路的當前和未來擴張正在吸引尋求成本效益和品質的全球公司。到 2024 年,中國和日本的市場規模將分別達到 1.475 億美元和 1.004 億美元,進一步鞏固其市場地位。
本報告分析了全球體外安全藥理學分析市場,並提供了市場定義和概述、影響市場成長的各種因素分析、市場規模趨勢和預測、按不同細分市場、地區和主要國家/地區劃分的市場細分、競爭格局以及主要公司的簡介。
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.