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市場調查報告書
商品編碼
1843688
2025年全球電子臨床結果評估(eCOA)、電子資料來源(eSource)和臨床試驗市場報告eCOA, eSource And Clinical Trials Global Market Report 2025 |
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近年來,電子臨床結果評估 (eCOA)、電子資料來源 (eSource) 和臨床試驗市場規模呈現強勁成長,預計將從 2024 年的 478.3 億美元成長至 2025 年的 511.5 億美元,複合年成長率 (CAGR) 為 6.9%。這一成長可歸因於臨床試驗中電子數據收集的普及、電子臨床結果評估 (eCOA) 監管標準的不斷完善、移動和穿戴式醫療技術的蓬勃發展、臨床試驗規模和複雜性的日益增加,以及臨床研究中對以患者為中心的理念的重視。
預計未來幾年,電子臨床結果評估 (eCOA)、電子資料來源 (eSource) 和臨床試驗市場將保持強勁成長,到 2029 年市場規模將達到 739.9 億美元,年複合成長率(CAGR)為 9.7%。預測期內的成長可歸因於全球臨床試驗網路的擴張、對即時數據訪問和監測需求的不斷成長、雲端基礎的電子臨床解決方案的開發、遠程和虛擬病患監測解決方案的成長、電子患者報告結果 (ePRO) 的日益普及、對用於持續患者病患監測的穿戴式設備的需求不斷成長、用於病人參與的行動醫療應用程式的快速普及,以及用戶對中心的生態預測期內的關鍵趨勢包括生態系統解決方案的技術進步、採用區塊鏈技術實現安全透明的臨床數據管理、在臨床研究中採用人工智慧進行數據分析、將機器學習整合到臨床試驗中進行預測分析,以及去中心化臨床試驗生態系統的發展。
電子臨床結果評估 (eCOA) 指的是臨床試驗和各種醫療保健研究環境中,利用電子方法和技術來收集、管理和分析臨床結果評估數據。同時,電子資料來源 (eSource) 指的是利用電子系統來收集、管理和儲存臨床試驗過程中產生的資料。臨床試驗是一項旨在評估新醫療干預措施的安全性、有效性和療效的研究。透過整合 eCOA 和 eSource,臨床試驗可以提高資料收集和管理流程的效率、準確性和可靠性。
eCOA、eSource 和臨床試驗解決方案中包含的關鍵解決方案包括 eCOA(電子臨床結果評估)、eSource、臨床試驗解決方案和電子資料收集 (EDC)。這些解決方案面向各類最終用戶,包括醫院、醫療保健提供者、CRO(委外研發機構)、製藥、生物技術和醫療設備業,並且可以部署在授權企業(本地部署)和雲端基礎(SaaS)環境中。
美國在2025年春季突然提高關稅及其引發的貿易摩擦,對資訊科技產業,特別是硬體製造、資料基礎設施和軟體部署領域,產生了重大影響。進口半導體、電路基板和網路設備的關稅上漲,推高了高科技公司、雲端服務供應商和資料中心的生產和營運成本。在全球範圍內採購筆記型電腦、伺服器和消費電子產品零件的公司,面臨更長的前置作業時間和價格壓力。同時,對專用軟體徵收的關稅以及主要國際市場的報復性措施,擾亂了全球IT供應鏈,並降低了海外對美國製造技術的需求。為了應對這些挑戰,該產業正在加大對國內晶片生產的投資,擴大供應商網路,並利用人工智慧驅動的自動化技術來增強韌性,更有效地控制成本。
這份《電子臨床結果評估 (eCOA)、電子資源 (eSource) 和臨床試驗市場研究報告》是商業研究公司最新報告系列的一部分,提供 eCOA、eSource 和臨床試驗市場統計數據,例如全球市場規模、區域佔有率、競爭對手及其市場佔有率、詳細的市場細分、市場趨勢和商業機會。這份 eCOA、eSource 和臨床試驗市場研究報告對該行業的現狀和未來發展趨勢進行了詳細分析,為您提供所需的一切全面觀點。
未來五年9.7%的成長率預測較我們先前的預測略微下調了0.2%。這一下調主要是因為美國與其他國家之間的關稅影響。關稅可能會增加用於分散式臨床試驗的數位平板電腦和加密行動平台的成本,這些設備通常從東亞供應商進口,從而擾亂臨床資料收集流程。此外,由於相互關稅以及不斷升級的貿易緊張局勢和限制措施對全球經濟和貿易造成的負面影響,其影響範圍也將更加廣泛。
預計臨床試驗數量的激增將推動電子臨床結果評估(eCOA)、電子資料來源(eSource)和臨床試驗市場的成長。臨床試驗是評估新型醫療干預措施和治療方法的安全性和有效性的研究,而eCOA和eSource解決方案的應用將使臨床試驗受益匪淺。 eCOA解決方案利用創新技術收集臨床結果數據,取代了傳統的紙本病患報告結果。例如,美國國家醫學圖書館營運的美國臨床試驗註冊機構ClinicalTrials.gov在2023年6月發布的一份報告預測,到2023年,註冊試驗的數量將達到457,100項,較2020年的362,479項顯著成長。對更多臨床試驗日益成長的需求正在推動eCOA、eSource和臨床試驗市場的擴張。
雲端基礎方案的日益普及預計將推動電子臨床結果評估 (eCOA)、電子資料來源 (eSource) 和臨床試驗市場的未來成長。雲端基礎方案包括程式、儲存空間、按需服務、電腦網路以及其他可透過網際網路連接從共用雲端運算框架存取的服務。這些解決方案透過促進即時資料擷取、安全儲存和遠端訪問,簡化了臨床試驗中的電子臨床結果評估 (eCOA) 和電子資料來源流程,最終最佳化臨床試驗效率並確保資料準確性。例如,根據澳洲政府統計機構澳洲統計局 (ABS) 的數據,截至 2022 年 6 月 30 日的一年中,報告採用資訊和通訊技術 (ICT) 的公司數量從截至 2020 年 6 月 30 日的一年中的 69% 增加到 85%,其中 59% 與雲端運算相關。因此,雲端基礎結果評估 (eCOA)、電子資料來源 (eSource) 和臨床試驗市場成長的因素。
技術進步是推動電子臨床結果評估 (eCOA)、電子資料收集 (eSource) 和臨床試驗市場發展的重要趨勢。這些市場的主要企業正積極採用創新技術以保持競爭力。例如,2022 年 5 月,總部位於美國的電子資料擷取解決方案開發商 Clinical Research IO 發布了 CRIO Reviewer,這是業界首個旨在建立完全整合的電子資料收集或電子資料擷取 (EDC) 系統的解決方案。此解決方案利用 CRIO 的基於 Web 的資源技術,簡化了 CRIO 電子資料擷取應用程式中收集的資料的審核和編碼,從而最佳化了臨床試驗中心的臨床資料管理工作流程。作為第一個專為臨床實驗中心流程設計的商用系統,CRIO Reviewer 旨在讓臨床實驗中心更方便地進行即時電子資料擷取。
電子臨床結果評估 (eCOA)、電子資料來源 (eSource) 和臨床試驗市場的主要企業正致力於實施電子健康記錄(EHR) 資料來源解決方案,以簡化資料收集、提高準確性並最佳化臨床試驗流程。 EHR 資料來源解決方案是指一種系統或技術,它能夠直接從電子資料來源(例如 EHR)收集、整合和使用健康數據,用於研究、臨床試驗和監管目的。例如,總部位於美國的 OpenClinica, LLC 於 2022 年 1 月推出了 EHR 資料來源解決方案 OpenClinica Unite。該平台使研究團隊能夠一鍵將 EHR 中的患者資料預先填充到電子病例報告表 (eCRF) 中,從而減少手動資料輸入時間並最大限度地減少轉錄錯誤。 OpenClinica Unite 透過確保電子資料擷取 (EDC) 系統中的資料與 EHR 中的資料相匹配,而無需對這些資料進行來源資料檢驗(SDV),從而獲得更準確、更全面的資料集。
2023年8月,總部位於美國的Sitero LLC收購了Clario的eClinical技術套件,具體金額未揭露。此次收購使Sitero得以整合Clario的電子臨床結果評估(eCOA)、電子資料來源(eSource)和臨床試驗的專業知識,從而擴展了其產品組合。 Clario是一家總部位於美國的科技公司,其創新的eCOA和eSource解決方案正為推動臨床試驗的發展做出重大貢獻。
eCOA、eSource 和臨床試驗市場的主要企業包括國際商業機器公司、甲骨文公司、美國實驗室控股公司、IQVIA 公司、Icon PLC、PPD 公司、Syneos Health 公司、Parexel 國際公司、Medpace Holdings 公司、TransPerfect Life Sciences 公司、Medidata Solutions 公司、Signant Health Private Limiteds、Signant Health 公司、Signant Health Private、Signa 公司公司、Kayentis SAS 公司、YPrime LLC 公司、Clinical Ink 公司、Cloudbyz 公司、Medrio 公司、OpenClinica LLC 公司、Castor EDC 公司和 Clinipace 公司。
2024年,北美是eCOA、eSource和臨床試驗市場最大的地區。 eCOA、eSource和臨床試驗市場報告涵蓋的地區包括亞太地區、西歐、東歐、北美、南美以及中東和非洲。
eCOA、eSource 和臨床試驗市場報告涵蓋的國家包括澳洲、巴西、中國、法國、德國、印度、印尼、日本、俄羅斯、韓國、英國、美國、義大利、西班牙和加拿大。
電子臨床結果評估 (eCOA)、電子資料來源 (eSource) 和臨床試驗市場包括營業單位提供預先建構評估、即時病患資料和計劃文件所獲得的收入。市場價值包括服務供應商銷售或包含在服務產品中的相關商品的價值。僅包括營業單位之間交易或銷售給最終消費者的商品和服務。
Electronic Clinical Outcome Assessment (eCOA) involves employing electronic methods and technologies for the collection, management, and analysis of clinical outcome assessment data in clinical trials and various healthcare research settings. Simultaneously, eSource refers to the utilization of electronic systems to capture, manage, and store data generated during clinical trials. Clinical trials, which are research studies designed to assess the safety, efficacy, and effectiveness of new medical interventions, benefit from the incorporation of eCOA and eSource, enhancing the efficiency, accuracy, and reliability of data collection and management processes.
The primary solution categories encompassed by eCOA, eSource, and clinical trials include eCOA (Electronic Clinical Outcome Assessment), eSource, clinical trial solutions, and electronic data capture (EDC). eCOA, specifically, entails utilizing electronic systems and devices to capture, manage, and analyze patient-reported outcome measures within clinical trials and healthcare settings. This solution can be deployed in both licensed enterprise (on-premise) and cloud-based (SAAS) environments, catering to diverse end users such as hospitals, healthcare providers, Contract Research Organizations (CROs), the pharmaceutical industry, the biotechnology industry, the medical device industry, and others.
Note that the outlook for this market is being affected by rapid changes in trade relations and tariffs globally. The report will be updated prior to delivery to reflect the latest status, including revised forecasts and quantified impact analysis. The report's Recommendations and Conclusions sections will be updated to give strategies for entities dealing with the fast-moving international environment.
The sharp rise in U.S. tariffs and the ensuing trade tensions in spring 2025 are having a significant impact on the information technology sector, especially in hardware manufacturing, data infrastructure, and software deployment. Increased duties on imported semiconductors, circuit boards, and networking equipment have driven up production and operating costs for tech companies, cloud service providers, and data centers. Firms that depend on globally sourced components for laptops, servers, and consumer electronics are grappling with extended lead times and mounting pricing pressures. At the same time, tariffs on specialized software and retaliatory actions by key international markets have disrupted global IT supply chains and dampened foreign demand for U.S.-made technologies. In response, the sector is ramping up investments in domestic chip production, broadening its supplier network, and leveraging AI-powered automation to improve resilience and manage costs more effectively.
The eCOA, eSource and clinical trials market research report is one of a series of new reports from The Business Research Company that provides eCOA, eSource and clinical trials market statistics, including eCOA, eSource and clinical trials industry global market size, regional shares, competitors with a eCOA, eSource and clinical trials market share, detailed eCOA, eSource and clinical trials market segments, market trends and opportunities, and any further data you may need to thrive in the eCOA, eSource and clinical trials industry. This eCOA, eSource and clinical trials market research report delivers a complete perspective of everything you need, with an in-depth analysis of the current and future scenario of the industry.
The ecoa, esource and clinical trials market size has grown strongly in recent years. It will grow from $47.83 billion in 2024 to $51.15 billion in 2025 at a compound annual growth rate (CAGR) of 6.9%. The growth in the historic period can be attributed to adoption of electronic data capture in clinical trials, evolution of regulatory standards for electronic clinical outcome assessments (ecoa), growth of mobile and wearable health technology, increase in complexity and scale of clinical trials, emphasis on patient-centric approaches in clinical research.
The ecoa, esource and clinical trials market size is expected to see strong growth in the next few years. It will grow to $73.99 billion in 2029 at a compound annual growth rate (CAGR) of 9.7%. The growth in the forecast period can be attributed to expansion of global clinical trial networks, rise in demand for real-time data access and monitoring, development of cloud-based eclinical solutions, growth of remote and virtual patient monitoring solutions, increase in the use of electronic patient-reported outcomes, rise in demand for wearables for continuous patient monitoring, surge in adoption of mobile health apps for patient engagement, emphasis on user-friendly and patient-centric ecoa designs. Major trends in the forecast period include technological advancements in esource solutions, adoption of blockchain for secure and transparent clinical data management, adoption of artificial intelligence for data analysis in clinical research, integration of machine learning for predictive analytics in clinical trials, development of decentralized clinical trial ecosystems.
The forecast of 9.7% growth over the next five years reflects a slight reduction of 0.2% from the previous projection. This reduction is primarily due to the impact of tariffs between the US and other countries. Tariffs may disrupt clinical data collection workflows by increasing costs for digital tablets and encrypted mobile platforms used in decentralized clinical trials, often imported from East Asian suppliers. The effect will also be felt more widely due to reciprocal tariffs and the negative effect on the global economy and trade due to increased trade tensions and restrictions.
The anticipated surge in clinical trials is expected to drive the growth of the eCOA, eSource, and clinical trials market. Clinical trials, which are research studies assessing the safety and efficacy of new medical interventions or treatment approaches, can benefit from the use of eCOA and eSource solutions. These technologies enable pharmaceutical companies to expedite trials, conducting them more efficiently within shorter time frames. eCOA solutions replace traditional paper-based patient-reported outcomes by employing innovative technologies for collecting clinical outcome data. For example, a report published on ClinicalTrials.gov in June 2023, a US-based registry of clinical trials run by the United States National Library of Medicine, projects the number of registered studies to reach 457,100 in 2023, a substantial increase from 362,479 in 2020. Thus, the growing demand for more clinical trials is a driving force behind the expansion of the eCOA, eSource, and clinical trials market.
The increasing adoption of cloud-based solutions is poised to propel the future growth of the eCOA, eSource, and clinical trials market. Cloud-based solutions encompass programs, storage spaces, on-demand services, computer networks, and other services accessible through a shared cloud computing framework via an internet connection. These solutions streamline eCOA (electronic Clinical Outcome Assessments) and eSource in clinical trials by facilitating real-time data capture, secure storage, and remote accessibility, ultimately optimizing trial efficiency and ensuring data accuracy. As an example, according to the Australian Bureau of Statistics in June 2023, an Australia-based government agency for statistics, 85% of firms reported employing information and communication technologies (ICTs) for the year ending June 30, 2022, up from 69% during the year ending June 30, 2020, with 59% related to cloud computing. Hence, the increasing adoption of cloud-based solutions is a driving factor for the growth of the eCOA, eSource, and clinical trials market.
Technological advancements constitute a prominent trend gaining traction in the eCOA, eSource, and clinical trials market. Leading companies in these markets are actively engaged in introducing innovative technologies to maintain their competitive positions. For example, in May 2022, Clinical Research IO, a US-based developer of eSource solutions, unveiled CRIO Reviewer, an industry-first solution designed to establish a fully integrated eSource or EDC (electronic data capture) system. This solution facilitates the review and coding of data collected by the CRIO eSource application, utilizing CRIO's web-based resource technology to optimize site workflows in clinical data management. As the first commercial system designed for site processes, CRIO Reviewer aims to make real-time electronic data gathering more accessible for sites.
Major companies in the eCOA, eSource, and clinical trials market are concentrating on introducing electronic health record (EHR) eSource solutions to streamline data collection, enhance accuracy, and improve the efficiency of clinical trial processes. An EHR eSource solution refers to a system or technology that facilitates the direct collection, integration, and use of health data from electronic sources, such as EHRs, for research, clinical trials, and regulatory purposes. For example, in January 2022, OpenClinica, LLC, a US-based company, launched OpenClinica Unite, an EHR eSource solution. This platform allows research teams to pre-populate electronic case report forms (eCRFs) with patient data from EHRs with a single click, reducing the time spent on manual data entry and minimizing transcription errors. By ensuring that the data in the electronic data capture (EDC) system aligns with that in the EHR, OpenClinica Unite removes the need for source data verification (SDV) for those items, resulting in more accurate and comprehensive datasets.
In August 2023, Sitero LLC, a US-based company, acquired Clario's eClinical technology suite for an undisclosed sum. This acquisition enables Sitero to broaden its portfolio by integrating Clario's expertise in electronic Clinical Outcome Assessment (eCOA), eSource, and clinical trials. Clario Co. is a US-based company that significantly contributes to the advancement of clinical trials through its innovative eCOA and eSource solutions.
Major companies operating in the eCOA, eSource and clinical trials market include The International Business Machines Corporation, Oracle Corporation, Laboratory Corporation of America Holdings, IQVIA Inc., Icon PLC, PPD Inc., Syneos Health Inc, Parexel International Corporation, Medpace Holdings Inc., TransPerfect Life Sciences, Medidata Solutions Inc., Signant Health Private Limited, Clario, Advarra Inc., Medable Inc., ArisGlobal LLC, Kayentis SAS, YPrime LLC, Clinical Ink, Cloudbyz Inc., Medrio Inc., OpenClinica LLC, Castor EDC, Clinipace Inc.
North America was the largest region in the eCOA, eSource and clinical trials market in 2024. The regions covered in the ecoa, esource and clinical trials market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa
The countries covered in the ecoa, esource and clinical trials market report are Australia, Brazil, China, France, Germany, India, Indonesia, Japan, Russia, South Korea, UK, USA, Italy, Spain, Canada.
The eCOA, eSource, and clinical trials markets include revenues earned by entities by providing pre-built assessments, real-time patient data, and project documentation. The market value includes the value of related goods sold by the service provider or included within the service offering. Only goods and services traded between entities or sold to end consumers are included.
The market value is defined as the revenues that enterprises gain from the sale of goods and/or services within the specified market and geography through sales, grants, or donations in terms of the currency (in USD, unless otherwise specified).
The revenues for a specified geography are consumption values that are revenues generated by organizations in the specified geography within the market, irrespective of where they are produced. It does not include revenues from resales along the supply chain, either further along the supply chain or as part of other products.
eCOA, eSource And Clinical Trials Global Market Report 2025 from The Business Research Company provides strategists, marketers and senior management with the critical information they need to assess the market.
This report focuses on ecoa, esource and clinical trials market which is experiencing strong growth. The report gives a guide to the trends which will be shaping the market over the next ten years and beyond.
Where is the largest and fastest growing market for ecoa, esource and clinical trials ? How does the market relate to the overall economy, demography and other similar markets? What forces will shape the market going forward, including technological disruption, regulatory shifts, and changing consumer preferences? The ecoa, esource and clinical trials market global report from the Business Research Company answers all these questions and many more.
The report covers market characteristics, size and growth, segmentation, regional and country breakdowns, competitive landscape, market shares, trends and strategies for this market. It traces the market's historic and forecast market growth by geography.
The forecasts are made after considering the major factors currently impacting the market. These include the technological advancements such as AI and automation, Russia-Ukraine war, trade tariffs (government-imposed import/export duties), elevated inflation and interest rates.