-

Global $1.6B Clinical Trial Management Systems Market, 2026 - Adoption of Decentralized Trials has Slowly Become a Must-Have rather than a Good-To-Have Initiative - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Global Clinical Trial Management Systems Market" report has been added to ResearchAndMarkets.com's offering.

The global market for clinical trial management systems was valued at $920.8 million in 2021. The market is expected to grow at a compound annual growth rate (CAGR) of 12.2%, to reach $1.6 billion by 2026. The global market is mainly driven by the increasing adoption of CTMSs in clinical trials and the rise of research and development (R&D) expenses of CRO. The fast spread of the coronavirus COVID-19 is also seen as another primary driver in the need for CTMS platforms.

The need to adopt patient-centric clinical trials has never been more acute for global pharmaceutical organizations. One of the greatest learnings from the COVID-19 pandemic was the tremendous potential held by digital technologies to enable remote and personalized clinical trials, also referred to as "decentralized" trials, to achieve trial continuity and operational efficiencies. With the advancement in technology, proactive guidance from regulators and a surge in wearable and devices, the adoption of decentralized trials has slowly become a must-have rather than a good-to-have initiative.

With the use of CTMS healthcare systems, professionals can easily access centralized data, thereby reducing the number of delayed trials. It can also handle site recruitment and identification while simultaneously providing control and tracking over subjects' databases and subject enrolment.

Market Dynamics

  • Drivers
    • Increased Outsourcing of Clinical Trials
    • Growing Number of Clinical Trials
    • Rising R&D Expenditure of Biopharma Companies
    • Increasing Prevalence of Chronic Diseases
  • Restraints
    • Unreliable and Inaccurate Data
    • Complex and Poorly-Integrated Systems
    • Regulatory Barriers and Approval Delays

Report Scope

This report examines the current and forecasted market potential for clinical trial management systems. It offers a detailed analysis of the market background, technological advancement, competitive environment, drivers and restraints, and market growth trends. This report includes market projections through 2026, detailing the market share for clinical trial management systems based on the product, deployment and delivery mode.

The clinical trial management systems product market is segmented into software and services. The clinical trial management systems deployment market is segmented into enterprise-based CTMS and site-based CTMS. The clinical trial management systems delivery market is segmented into web-based, cloud-based and on-premises services.

The clinical trial management systems market has been geographically segmented into Europe, North America, the Asia-Pacific (APAC) region and the Rest of the World (RoW). The detailed analyses of major countries such as the U.S., Germany, Canada, the U.K., Spain, Italy, France, Japan, India and China are regional segments. For market estimates, data are provided for 2020 as the base year, and then forecast from 2021 through year-end 2026. Estimated values are based on clinical trial management systems companies' total revenues. Projected and forecast revenue values are in constant U.S. dollars that have not been adjusted for inflation.

The report includes:

  • An overview of the global markets for clinical trial management systems
  • Estimation of the market size and analyses of market trends, with data from 2019 to 2020, estimates for 2021 and projection of CAGR through 2026
  • Quantification of clinical trial management systems market based on product type, deployment, delivery mode and region, and analysis of market drivers, restraints and other forces impacting the global market
  • Highlights of the current and future market potential and insights into government initiatives, regulatory framework and reimbursement scenario
  • Detailed description of the advanced technologies for clinical trial management systems and discussion on how they are advantageous to pharmaceuticals, biotech and other research-focused life sciences organizations
  • Market share analysis of the key companies of the industry and coverage of events like mergers & acquisitions, joint ventures, collaborations or partnerships and other key market strategies and a relevant patent analysis
  • Company profiles of major players, including Advarra, Calyx, DatStat, Medidata and Oracle

Companies Profiled

  • Advarra
  • BSI Business Systems Integration AG
  • Calyx
  • Clario
  • Datstat (R1 Company)
  • Datatrak Int
  • Ennov
  • Medidata Solution Inc. (Dassault Systemes)
  • Oracle
  • Realtime Software Solutions LLC
  • Veeva Systems Inc.

For more information about this report visit https://www.researchandmarkets.com/r/nskkpd

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com

For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

Research and Markets


Release Versions

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com

For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

More News From Research and Markets

Computer System Validation (CSV) Training Course: Regulations Impacting Your Systems and Hands-on Practice Writing Validation Documents (Jan 27th - Jan 29th, 2026 & On-Demand) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation (CSV) Training Course (Jan 27th - Jan 29th, 2026)" training has been added to ResearchAndMarkets.com's offering. A course designed to completely immerse you in computer system validation. This course delivers comprehension of the regulations impacting your systems and hands-on practice writing validation documents. You will leave ready to lead efficient, effective, inspection- ready validation projects. Registration Includes: Checklist of...

Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions Webinar - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions (January 15, 2026)" training has been added to ResearchAndMarkets.com's offering. This expert-led 3-hour webinar provides a comprehensive introduction to the key regulatory pathways for medical device submissions in the US market. The regulation and control of new or substantially changed medical devices for sale in the US is based on the 510(k), PMA or DeNovo submission process. This w...

Medical Devices: Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) Course: Developing Effective Post Market Surveillance and Complaint Handling Systems Training - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course (Jan 22nd - Jan 23rd, 2026)" training has been added to ResearchAndMarkets.com's offering. What are U.S. FDA CGMP expectations/requirements for Post Market Surveillance and Complaint Handling? This seminar will examine Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), as well as appropriate articles / Annexes of the EU's MDR, which require manu...
Back to Newsroom