ePRO Resources

  1. Mitigating The Risks Of Long-Term Oncology eCOA Clinical Trials 6/23/2022

    This article digs into the specific complexities of long oncology clinical trials and describes relevant solutions to manage the risks regarding patient compliance, clinical project teams, and clinical sites.

  2. ePROM Implementation: 4 Best Practices For System Functionality 2/13/2024

    Explore four of the 15 system functionality considerations highlighted in an eCOA Consortium article that aim to create a more thorough and standardized approach to ePROM implementation.

  3. Increase Participant Diversity With eClinical Tools 4/14/2023

    The right technology and community partnerships can help sponsors meet FDA diversity requirements without additional expenditures, build relationships with minorities, and prepare for future trials.

  4. Site Perspectives On BYOD ePRO Use 6/17/2024

    This study examines participant convenience and compliance, aiming to understand and address the challenges faced by site personnel in global trials.

  5. Headed Down Registry Road? Here Are The EDC Features You'll Need 3/18/2022

    Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.

  6. The Benefits Of Real-Time ePRO/eCOA In Clinical Trials 10/4/2024

    TrialKit addresses data management issues in clinical trials through its innovative ePRO and eCOA tools, which facilitate real-time data collection and reporting.

  7. 3 Steps To Improve Site Acceptance Of ePRO In Medical Device Trials 3/6/2023

    Discover how with the proper understanding of a site’s barriers, early engagement, and prioritizing effective training, site acceptance of ePRO can be improved.

  8. How Site And Patient Research Optimizes Clinical Trials 6/17/2024

    Signant’s patient and site research enhances digital health technology in clinical trials by optimizing usability and design. These insights drive improvements in product features, study designs, and training materials.

  9. Benefits Of Using ePRO In Early Phase Studies 3/24/2023

    Discover how harnessing Patient Reported Outcomes electronically in early-phase trials can boost patient centricity, create more cost-effective operations, and help generate better data faster.

  10. Why Capturing Pro Data Matters In Early-Phase Oncology Trials 9/26/2024

    If you are in the early stages of an oncology trial, there is a lot to consider when it comes to your data management and how the process can be simplified by improving how your study captures data.