Patient Data Reporting White Papers & Articles

1. Why The Everest Group Named Medable A Leader In eCOA 2/2/2026

   Discover how this eCOA is leading the charge in accelerating study timelines, boosting patient engagement, and answering real sponsor needs.

2. Navigating The Post-Capture Era Of Clinical Trials 2/2/2026

   Liberating data through structured workflow management is the key to evolving clinical trials from a series of administrative hurdles into a high-speed engine for medical innovation.

3. Improving The eCOA Experience 1/25/2026

   Discover how template-driven builds and reuse can slash eCOA timelines by 50% while solving the licensing and translation hurdles that delay First Patient In.

4. The Value Of Patient-Reported Outcomes In Cancer Clinical Research 1/16/2026

   Standardizing patient-reported outcomes and real-time monitoring transforms the patient voice into a powerful tool for regulatory success and superior clinical care.

5. Clinical Development Crystal Ball: What To Watch In 2026 1/16/2026

   Explore how AI integration, remote assessment, and precision measurement are reshaping clinical trials in 2026 to improve data quality and patient outcomes.

6. Quantifying Potential: Leveraging Data To Showcase Biotech Value 1/14/2026

   Biotechs must use data-driven insights to prove asset potential. Real-world evidence and predictive analytics validate differentiation, forecast market opportunity, and build investor confidence.

7. FDA Pushes For Patient Voice: ePRO In Oncology Trials 1/8/2026

   FDA urges sponsors and CROs to include patient voices in oncology trials. Discover why it matters and how to start integrating this approach.

8. Meeting Your Clinical Trial Enrollment Target Without Delays 1/6/2026

   Bridge the enrollment gap by blending site-based tactics with global direct-to-patient outreach. Use digital screening and EMR intelligence to ensure faster, more predictable paths to randomization.

9. Virtual eConsent For Decentralized Trials 12/23/2025

   Virtual eConsent improves accessibility and compliance in decentralized trials, streamlining enrollment with a secure, user-friendly process for informed consent in remote research.

10. Streamlining Trials With eConsent And EDC 12/23/2025

    Integrating eConsent with EDC streamlines clinical workflows, improves data accuracy, and enhances patient engagement by creating a unified, compliant system for consent and trial data management.