Patient Data Reporting White Papers & Articles
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Digital Tools And Technologies Used To Improve Clinical Trial Recruitment
7/17/2025
Digital clinical trial recruitment is revolutionizing patient engagement. Discover how cutting-edge technologies are reshaping recruitment strategies and transforming the future of global healthcare.
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The Role Of AI In Enhancing Patient Screening For Clinical Trials
7/17/2025
AI is transforming clinical trials by streamlining patient recruitment and screening. Discover how advanced technologies are accelerating research and bringing life-saving treatments to market faster.
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CDISC + TMF Europe Interchange 2025: 5 Key Takeaways
7/14/2025
The CDISC + TMF Europe Interchange showcased critical insights for TMF professionals. Learn about essential collaboration, the impact of AI, and the continued drive for standardization in clinical trials.
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New EDC Tools Enable Even Faster Self-Serve Study Builds
7/10/2025
Explore a powerful yet accessible EDC solution that enables faster, more efficient study builds without compromising data integrity or compliance, allowing clinical teams to focus on advancing research outcomes.
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Optimizing The Rater Journey
7/10/2025
For scalable CNS trials, central rating models, where a select group of expert raters conduct remote assessments, offer a way to standardize data collection globally while enhancing patient accessibility and inclusion.
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The Top 5 Myths About eCOA In 2025
7/7/2025
Projected to grow 16.1% annually through 2030, eCOA solutions are booming. Uncover the top five myths and misconceptions about eCOAs in 2025 so your clinical teams can make evidence-based decisions.
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Modern Post-Market Trials Driven By RWD – Is Your EDC Ready?
7/7/2025
Explore the transformative role of real-world data (RWD) and advanced Electronic Data Capture (EDC) systems in post-market research, marking a departure from traditional Phase IV trials.
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How EDC-Based SAE Reporting Reduces Time To Detection And Response
7/7/2025
Serious adverse events (SAEs) play a pivotal role in patient safety during clinical trials, and the right EDC system helps you efficiently track and manage the entire lifecycle of SAE reporting.
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Central eSource Is The Latest In Sponsor Provided Site Offerings
7/7/2025
For decades, sponsors have provided tools to help clinical sites work more efficiently. Central eSource is the latest evolution in this trend.
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eSource Purpose Is Not Just To Complete The EDC
7/7/2025
Central eSource transforms data capture from a passive, back-end chore into an active, real-time quality and compliance engine—delivering benefits that extend beyond faster EDC feeds and reduced SDV.