eCOA, eSource And Clinical Trials Market Growth Trajectory Through 2024-2033

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The eCOA, eSource And Clinical Trials Global Market Report 2024 by The Business Research Company provides market overview across 60+ geographies in the seven regions – Asia-Pacific, Western Europe, Eastern Europe, North America, South America, the Middle East, and Africa, encompassing 27 major global industries. The report presents a comprehensive analysis over a ten-year historic period (2010-2021) and extends its insights into a ten-year forecast period (2023-2033).

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According to The Business Research Company’s eCOA, eSource And Clinical Trials Global Market Report 2024, The ecoa, esource & clinical trials market size has grown strongly in recent years. It will grow from $44.85 billion in 2023 to $48.94 billion in 2024 at a compound annual growth rate (CAGR) of 9.1%. 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 & clinical trials market size is expected to see strong growth in the next few years. It will grow to $67.33 billion in 2028 at a compound annual growth rate (CAGR) of 8.3%. 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 growing demand for more clinical trials is expected to propel the growth of the eCOA, eSource and clinical trials market. Clinical trials refer to research studies conducted to evaluate the safety, efficacy, and effectiveness of new medical interventions or treatment approaches. The use of eSource and eCOA solutions helps pharmaceutical companies speed up trials and conduct more trials in less time. eCOA solutions replace traditional paper-based, patient-reported outcomes by using innovative technologies to collect clinical outcome data. For instance, in June 2023, according to a report published on ClinicalTrials.gov, a US-based registry of clinical trials run by the United States National Library of Medicine, the number of registered studies will be 457,100 in 2023, representing a significant increase from 362,479 in 2020. Therefore, the growing demand for more clinical trials is driving the growth of the eCOA, eSource and clinical trials market.

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The ecoa, esource and clinical trials market covered in this report is segmented –

1) By Solution Type: eCOA (Electronic Clinical Outcome Assessment), eSource, Clinical Trial Solutions, Electronic Data Capture (EDC)

2) By Deployment: Licensed Enterprise (On-premise), Cloud-Based (SaaS)

3) By End User: Hospital, Healthcare Providers, CROs, Pharmaceutical Industry, Biotechnology Industry, Medical Device Industry, Other End Users

Technological advancements are a key trend gaining popularity in the eCOA, eSource and clinical trials market. Major companies operating in the eCOA, eSource, and clinical trials markets are focused on introducing innovative technologies to sustain their position in the market. For instance, in May 2022, Clinical Research IO, a US-based eSource solutions developer, launched CRIO Reviewer, an industry-first solution designed to create a fully integrated eSource or EDC (electronic data capture) system. This solution helps users review and code the data that is collected by the CRIO eSource application. It leverages CRIO’s web-based resource technology to optimize site workflows in clinical data management. It is a user-friendly web-based technology that was the first commercial system to be designed for site processes, making it easier for sites to embrace real-time electronic data gathering.

The ecoa, esource and clinical trials market report table of contents includes: