Featured Articles

1. Unified Patient Apps: The Future Of Trial Simplicity 11/12/2025

   A unified patient app streamlines clinical trial participation by combining scheduling, questionnaires, travel, and payments—reducing burden, improving engagement, and supporting better retention and data quality.

2. How Real-World Data On Site Costs Accelerates Clinical Trial Success 10/23/2025

   Outdated budgeting slows oncology trials. Real-world site cost data enables faster planning, smoother startup, and better patient care through smarter, evidence-based financial decisions.

3. eCOA In Oncology Trials: A Tool To Simplify 10/16/2025

   Accurate quality of life data is critical in oncology. eCOA unified with IRT streamlines trials, improves data collection, and enhances site user experiences across therapeutic areas.

4. Why Real-Time eCOA Data Matters More Than Ever 10/16/2025

   Real-time eCOA data enables faster eligibility decisions, proactive issue alerts, and streamlined operations by unifying data, improving precision, responsiveness, and trial execution efficiency.

5. A Merger Supporting A More Seamless Trial Experience 10/2/2025

   Clinical trials don’t have to be so complex. Jagath Wanninayake shares why focusing on time-sensitive moments—and not everything at once—can drive better outcomes and how a recent merger supports that shift.

6. Increasing Efficiency And Reducing Drug Waste 10/2/2025

   Discover how streamlined clinical supply chain management helped accelerate study timelines, reduce costs, and support global treatment delivery through a strategic technology partnership.

7. Accelerating Study Startups: Drive Efficiency From Protocol To Go-Live 9/15/2025

   Speed up trial launches and maintain predictable timelines by leveraging a modern, integrated approach to eCOA setup that reduces complexity.

8. Understanding Decentralized Clinical Trials: FDA vs. EMA Fundamentals 9/15/2025

   Designing a global decentralized clinical trial requires understanding the differing FDA and EMA approaches to trial models and informed consent.

9. Managing Drug And Data Requirements In Decentralized Clinical Trials 9/15/2025

   Running a global decentralized clinical trial requires a deep understanding of the differences in FDA and EMA requirements for investigational products and patient data.

10. 5 Essential Steps To Implementing Decentralized Clinical Trials Globally 9/15/2025

    Running a global decentralized clinical trial requires a strategy that balances the FDA's focus on technology accessibility with the EMA's emphasis on validation and comprehensive documentation.