ePRO/eCOA White Papers & Case Studies

  1. Hybrid eConsent: Remote And On-Site 3/21/2025

    Studies show when participants are informed and comfortable with the consent process, they're more likely to comply with protocol, remain enrolled, and contribute to faster study deployment.

  2. Safeguarding Personal Data: Protecting PII 3/17/2025

    Learn about a secure, patient-centric platform that enables individuals to participate in clinical trials and registries while maintaining lifelong access to their data.

  3. Medable's Japanese Clinical Trial Exceeds FPI Date And eCOA Adherence 3/10/2025

    A top-10 global pharma company aimed to address eCOA adherence and patient enrollment challenges faced by clinical trial sites in Japan. Explore an initiative to enhance the patient and site experience.

  4. GSK And Medable Discuss The Next Phase Of DCTs 3/10/2025

    GSK and Medable share the value of embedding DCTs into strategic goals to enhance trial accessibility, diversity, and efficiency.

  5. A Guide To Digital Endpoints In Major Depressive Disorder 3/7/2025

    The integration of digital health technologies (DHTs) in clinical trials for Major Depressive Disorder (MDD) is transforming how symptom severity and treatment efficacy are measured.

  6. The Evolution Of Technology For Safety Notifications 3/6/2025

    Discover how a digital-first approach empowers sponsors to optimize safety management and drive operational efficiency in an increasingly complex, global clinical landscape.

  7. Supporting Study Set Up In Just 4 To 6 Weeks 3/4/2025

    Facing challenges in cycle times, quality control, and visibility, a global CRO adopted Medidata’s Rave Imaging, integrating it with its existing Rave EDC system to create a seamless digital workflow.

  8. Biotech Delivers A Superior Patient And Site Experience 3/4/2025

    To become the sponsor of choice for sites and patients in congenital hyperinsulinism clinical trials, a small biotech company prioritized delivering a superior experience while streamlining operations.

  9. Accelerate Study Startup Through Better Collaboration 3/3/2025

    With 80% of trials failing to enroll patients on time, improved collaboration between sites and sponsors is essential.

  10. Evaluating Cognitive Safety In Clinical Trials 2/21/2025

    Understanding cognitive function is essential in drug development. Explore how you can utilize cognitive tests to evaluate treatment effects on cognition with unrivaled accuracy and sensitivity.