ePRO Resources

  1. Simple, Cost-Effective Ways To Engage Patients Using eCOA And IRT 9/7/2022

    Today, patients are exposed to sophisticated technology, which presents a huge opportunity to elevate engagement. Consider some common elements when initiating engagement during clinical development.

  2. Powering Your Research Potential: Elevating Participant Centric Research 4/19/2024

    This flexible, web-based solution offers patient-centric experiences, ensuring efficient data capture and immediate insights. Transform how you gather and manage trial data for superior accuracy and participant engagement.

  3. The AI-Native Platform For Modern Clinical Research 3/3/2025

    Join Curebase CEO Tom Lemberg for a live demo of our next-generation ePRO/eCOA technology. See how our AI Assistant lets you build forms, generate translations, and enter data in seconds with our intuitive, user-friendly platform.

  4. Rare Disease Clinical Trials: Modern Design And Supply Chain 10/12/2023

    Gain insight from several contributing experts for overcoming unique obstacles in rare disease research and learn how to better develop strategies.

  5. 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.

  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 Transformative Impact Of EDC Systems In 2025 5/6/2025

    The shift towards decentralized and hybrid trials underscores the significance of EDC in expanding geographic reach, fostering diversity in participant populations, and reduce participant burden.

  8. Driving Customer Profitability With Enterprise Platform, Pricing 2/29/2024

    Explore how the solutions and approaches offered by CDS can help different research stakeholders conduct more cost-efficient clinical trials in the industry's pharmaceutical, biotech, and device sectors.

  9. Why eConsent Makes Such A Difference In Patient Adherence And Engagement 6/6/2022

    Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.

  10. 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.