Patient Data Reporting White Papers & Articles

  1. Mid-Study Data Migrations: The Antidote To Longer Clinical Trials 1/22/2025

    As trial durations continue to grow, mid-study migrations are transforming from rare occurrences into a critical strategy for maintaining efficiency and data integrity in clinical research.

  2. How Technology Helps Clinical Trial Sites And Their Staff 1/22/2025

    eConsent is transforming clinical research sites by addressing key pain points and streamlining processes for overburdened staff.

  3. Transforming Clinical Trials Through Enhanced eConsent Technology 1/22/2025

    How can innovative eConsent solutions help you expand participant reach, diversity, and inclusivity while ensuring regulatory compliance in the ever-evolving landscape of clinical trials?

  4. Oncology Trials: Accuracy And Alleviating The Patient Screening Burden 1/17/2025

    Flatiron Health has unveiled an innovative service designed to enhance patient screening for clinical trials by integrating structured EHR data with machine learning and human analysis.

  5. Overcoming Issues Of Non-Enrolling Sites In Clinical Trials 1/14/2025

    Explore the challenges of non-enrolling sites in clinical trials, focusing on the benefits of leveraging artificial intelligence (AI) and machine learning (ML) in addressing those issues.

  6. The Evidence And Outcomes Of Decentralized Modalities 1/14/2025

    As trials continue to digitize, learn how connected sensors, COAs, and other data practices will come together to form the evidence of tomorrow—with proven, real-life examples.

  7. Solving Key eCOA Challenges Through Digital Trials—Proof Points! 1/14/2025

    Medable has reached some important milestones and shares them in its end-of-year report. Check it out to see what game-changing results they've brought to their customers.

  8. A Year Of Reflection And Preparation 1/3/2025

    The Trial Master File (TMF) landscape in 2025 will require companies to stay attuned to the evolving ICH E6(R3) guidelines and the full implementation of the CTIS.

  9. PIPA Conference Explores The Key Role Of PV 1/2/2025

    The PIPA 2024 conference emphasized the importance of pharmacovigilance across the pharmaceutical industry, from mergers and acquisitions to clinical trials and health authority inspections.

  10. Ensuring Timeliness, Completeness, And Quality With Digital Solutions 12/13/2024

    A well-maintained TMF, supported by digital solutions, is the backbone of successful clinical trials, improving trial management and readiness for audits or regulatory submissions.