The global market for electronic trial master file (eTMF) systems was valued at around USD 0.9 billion in 2019. Since then, demand for eTMF software and services has grown at an annual rate of 14.9%, reaching a market value of USD 1.5 billion in 2023. These systems facilitate real-time collaboration and accessibility, which has driven their popularity.
According to recent analysis, the market is projected to be worth $1.7 billion in 2024. The push for digital transformation in clinical trials and life science research has further boosted the eTMF industry in recent years.
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Over the next ten years, the adoption of electronic trial master file (eTMF) systems is expected to increase at a 12.9% CAGR. By the end of 2034, the electronic trial master file (eTMF) system industry is anticipated to have grown to US$ 5.8 Billion.
Key Takeaways from the Electronic Trial Master File (eTMF) System Market Report:
- The United States currently leads the market for electronic trial master file (eTMF) systems and is likely to advance at a CAGR of 13% through 2034.
- In Europe, the United Kingdom is expected to hold a lucrative market for eTMF service providers by advancing at 14.4% through 2034.
- China is currently the leading market for eTMF software development in Asia and is poised to progress at a rate of 13.3% per year through the forecast period.
- Japan and South Korea are two emerging markets for eTMF integration and are anticipated to follow 14.4% and 15.2% CAGRs through 2034.
Competitive Landscape for the Electronic Trial Master File (eTMF) System Market Participants:
Leading players like Veeva Systems, Aris Global, and Clinevo Technology hold a sizable market share, making it highly concentrated. However, the growing emphasis on regulatory compliance and clinical trial activities in emerging nations is likely to diversify the market with the emergence of new electronic trial master file service providers.
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Recent Developments by the Electronic Trial Master File (eTMF) System Market Players:
- In February 2023, Vial and Egnyte signed a collaboration agreement to integrate the Life Sciences eTMF technology into Vial’s platform. According to the clinical research organization Vial, Egnyte eTMF is a 21 CFR Part 11 compliant platform that improves audit preparedness for life sciences organizations, reduces document and data processing times, and maintains compliance.
- In April 2021, Phlexglobal eTMF vendor revealed five of the world’s top 10 pharmaceutical companies are using its cutting-edge TMF Quality Review solution. The firm claims that its TMF solution aids in better preparation for inspections, identify loopholes for clinical trials, and mitigates regulatory risk associated with their mergers and acquisitions.
Electronic Trial Master File (eTMF) System Market Segmentation:
By Component or Product Type:
- Software
- Services
By Deployment Type:
- On-Premise
- Cloud
By End User Verticals:
- Pharmaceutical & Biotechnology Companies
- Contract Research Organizations (CROs)
- Other End Users
By Functionality:
- Clinical Operations
- Records Management
- Auditing
- Information Technology (IT) Operations
- Other Functionalities
By Region:
- North America
- Latin America
- Europe
- East Asia
- South Asia and Pacific
- The Middle East and Africa (MEA)
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