ePRO Resources

  1. Why eSource: The Advantages of Abandoning Paper Records 2/16/2023

    Eliminate transcription errors and fully leverage supporting eClinical technology to provide a reliable consistent exchange of information.

  2. Empowering Freenome: Large-Scale Data Quality And Compliance 10/17/2023

    Delve into five ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.

  3. Mobile App And Wearable Integration Collects Longitudinal Data 2/12/2024

    Get an overview of SISCAPA's utilization of eTechnologies, specifically ePRO, and how their partnership with CDS accurately demonstrates the improvement of data collection and analysis in the biotechnology industry.

  4. Simplifying ePRO Data Collection 10/4/2024

    The Bring Your Own Device (BYOD) model, supported by Trialkit, is an innovative approach in clinical trials that allows participants to use personal smartphones or tablets for data collection.

  5. Focusing On Patient-Reported Outcome Measures And eConsent 8/7/2023

    Learn how digital solutions can contribute to a more participant-centered approach and potentially enhance the regulatory utility of PRO data while improving the overall quality and efficiency of oncology trials.

  6. Considerations For Implementing The Best eCOAs In Your Trial Design 5/2/2022

    Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.

  7. The Building Blocks Of DCT: How To Create A Seamless Experience Across eConsent, eCOA, And More 3/29/2022

    With more than 76% of sponsors seeking to implement decentralized solutions this year, there’s never been more attention given to decentralized trials. Discover why decentralized trials must take a unified approach, one that alleviates burdens for patients and sites in order to drive cost savings and realize efficiencies. 

  8. Creating Success With Digital Measures 8/2/2024

    Recent research from the Tufts Center for the Study of Drug Development (CSDD) illuminated the substantial ROI of digital endpoints in clinical trials. Discover how to transform your trials today.

  9. 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.

  10. ISR Report Sheds Light On eCOA/ePRO Market Dynamics 5/15/2024

    This comprehensive overview highlights the critical role these platforms play in modern clinical research, emphasizing their impact on data integrity and trial efficiency.