ePRO Resources

  1. Measuring The True Patient Experience 5/15/2024

    Utilizing the insights covered in this article can inform the design and implementation of cancer trials, ultimately contributing to improved patient care and treatment outcomes.

  2. Exploring Modular Mobile And Web ePRO 10/17/2023

    Review the capabilities of this collection of ePRO applications, available on both web and mobile platforms, for enhancing hybrid or decentralized clinical trial experiences.

  3. Designing ePRO and eConsent Solutions that Participants and Sites Want 10/26/2022

    Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value. 

  4. Balancing Clinical Care With Digital Utility In Hybrid Trials 10/24/2022

    To create an effective decentralized clinical trial, tools and methods must be considered within the context of challenges faced by the clinical trial’s patients, physicians, and sites.

  5. eCOA Predictions For 2022 5/2/2022

    Dive into the prediction that the rapid adoption of eCOAs will continue to grow in 2022, as sponsors acknowledge how useful these tools have become in decentralized clinical trial (DCT) settings.

  6. Evidence Generation Evolved 6/13/2024

    Explore how innovative strategies are cutting clinical trial times in half and accelerating the delivery of life-saving treatments.

  7. Increasing The Usefulness Of PROs In Oncology Research 2/20/2024

    Dr. Anthony Everhart (Clinical VP, Signant Health) and Tim Meyer (Professor, University College London) discuss opportunities for increasing the usefulness of PROMs.

  8. Veeva eCOA Demo 6/24/2024

    See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.

  9. Minimizing Hurdles For Patients During The eConsent Process 10/4/2022

    Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.

  10. Taking Advantage Of EMA CTR For eCOA Studies In EU 7/13/2023

    Discover how sponsors can save time and effort by applying for clinical trial authorization once across the EU using the Clinical Trials Information System (CTIS).