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市場調查報告書
商品編碼
1380468
全球體外毒理學測試市場 2023-2030Global In-Vitro Toxicology Testing Market 2023-2030 |
預計全球體外毒理學測試市場在預測期內將以 10.5% 的CAGR成長。藥物研究支出的大幅成長是推動體外毒理學測試成長的關鍵因素。由於製藥公司研發支出增加以及進入臨床前開發階段的新藥數量增加,體外毒理學測試的需求也隨之增加。臨床前管道產能的顯著增加以及人們對體外測試服務優勢的認知不斷增強,正在推動全球市場的成長。此外,動物試驗傳統上不斷上漲的成本及其社會倫理問題進一步促進了市場的成長。用於評估藥物安全性的體外測試方法的重大發展以及這些藥物對細胞和組織的潛在影響是市場成長的其他一些貢獻者。
為了滿足不斷成長的需求,主要參與者正在開設或投資新設施。例如,2023 年 4 月,製藥和營養輔料供應商羅蓋特 (Roquette) 在費城附近開設了新的製藥創新中心。這個耗資 2,500 萬美元的新中心將成為全球製藥和營養保健品製造商的高級培訓和合作中心。美國設施專注於最佳化下一代口服劑型的患者體驗,補充了羅蓋特在法國和新加坡現有的製藥創新中心的尖端研究活動。支持這些培訓課程和該中心主要研究項目的是一套最新的製藥加工、測試和製造設備。
Title: Global In-vitro toxicology testing Market Size, Share & Trends Analysis Report, by Technology (Cell Culture, High Throughput, Molecular Imaging, OMICS), by Method (Cellular Assay, Biochemical Assay, In Silica, Ex Vivo), by Application (Systematic Toxicology, Dermal Toxicity, Endocrine Disruption, Ocular Toxicity, Other Applications), by End-User (Pharmaceutical and Biotechnology, Diagnostics, Other End-Users)Forecast Period (2023-2030).
The global in-vitro toxicology testing market is anticipated to grow at a considerable CAGR of 10.5% during the forecast period. A considerable rise in pharmaceutical research expenditure is a key factor driving the growth of the in-vitro toxicology testing. Due to increased R&D expenditure by pharmaceutical companies as well as an increase in the number of novel medications entering the preclinical stage of development, there has also been an increase in demand for in-vitro toxicology testing. A significant increase in preclinical pipeline capacity along with growing awareness about the benefits of in-vitro testing services is driving the global market growth. In addition, the traditional rising cost of animal tests as well as their socio-ethical problems is further contributing to the market growth. Significant developments in the in-vitro testing assays used to evaluate the security of medicines and the potential impacts of those drugs on cells and tissues are some other contributors to the market growth.
To meet the growing demand key players are opening or investing new facilities. For instance, in April 2023, Roquette, a provider of pharmaceutical and nutraceutical excipients, opened its new pharmaceutical innovation center near Philadelphia. The new $25 million center will be an advanced training and collaboration hub for pharmaceutical and nutraceutical manufacturers across the globe. With a focus on optimizing patient experience with next-generation oral dosage forms, the US facility complements the cutting-edge research activities of Roquette's existing pharma innovation centers in France and Singapore. Underpinning these training sessions and the center's primary research projects is a suite of the latest pharmaceutical processing, testing, and manufacturing equipment.
In the same month, Millipore Sigma has invested $37.5 million to strengthen biosafety testing in Scotland. The investment includes a new 1200-m2 facility in Glasgow that will house molecular biology and sequencing services, and the company will add biosafety testing, analytical development, and viral clearance suites in its current buildings to expand testing capacity.
The global in-vitro toxicology testing market is segmented based on technology, method, application, and end-user. Based on technology, the market is segmented into in cell culture, high throughput, molecular imaging, and OMICS. Based on method, the market is sub-segmented into cellular assay, biochemical assay, in silica, and ex vivo. Based on application, the market is sub-segmented into systematic toxicology, dermal toxicity, endocrine disruption, ocular toxicity, and other applications. Based on end-user, the market is sub-segmented into pharmaceutical and biotechnology, diagnostics, and other end-users.
The cell culture technology segment held considerable share in 2022. The cell cultures provide reproducible results to consistent samples, and serve as excellent models for toxicology assays. Hence, it is highly adopted to perform toxicology testing. This technology further enables early stage drug toxicity testing due to which this technology is gaining popularity & extensive application across the globe.
The global in-vitro toxicology testing market is further segmented based on geography, including North America (the US and Canada), Europe (Italy, Spain, Germany, France, and others), Asia-Pacific (India, China, Japan, South Korea, and others), and the Rest of the World (the Middle East & Africa and Latin America). Asia-Pacific is anticipated to exhibit highest CAGR in the global in-vitro toxicology testing market. The rising investment by companies from emerging economies in enhancing regional healthcare is a key promoter to the regional market growth. Establishment of new healthcare facilities along with alliances formation with major laboratories is further contributing to the market growth.
North America held considerable share in in-vitro toxicology testing market in 2022. The regional market is driven by the presence of key in-vitro toxicology testing service providers. The rising investments in R&D for the development of novel therapeutics for chronic diseases are further contributing to the market growth. According to EFPIA member associations in 2020, the US has invested $72,412 million in pharmaceutical R&D. Besides, the region has a relatively high disposable income, which enables people to afford expensive drugs and medical treatments. This creates a strong demand for pharmaceutical products in the region; which is further contributing to the regional market growth.
The major companies serving the global in-vitro toxicology testing market include: Abbott Laboratories, Bio-Rad Laboratories, Laboratory Corporation of America Holdings, Agilent Technologies Inc., and Eurofins Scientific SE among others. The market players are considerably contributing to the market growth by the adoption of various strategies, including mergers and acquisitions, partnerships, collaborations, funding, and new product launches, to stay competitive in the market.