eConsent Resources

  1. Essity Uses eConsent To Optimize Enrollment 8/15/2023

    See how a global hygiene and health company was able to deploy virtual methods through a strategic partnership to recruit and retain participants, streamline consent, and analyze patient data.

  2. How eConsent Delivers Value For Sponsors 9/21/2023

    Delve into the data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials.

  3. 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.

  4. Tips For Tailoring eConsent For Optimal Patient Centricity 3/29/2022

    While informed consent is a critical process for ensuring participant autonomy, consent forms are too long, unclear, difficult to read, and frequently exceed 9th grade reading levels. Explore why eConsent is a potential solution to this problem.

  5. 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.

  6. Our Unified Platform Serves As eSource For COVID Treatment Trial 6/17/2024

    Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.

  7. Empowering Oncology Research With The Right Technology Solutions 10/25/2023

    Explore how advanced technology solutions have the potential to simplify the operational aspects of oncology trials.

  8. Linking Clinical Trial Data With Real-World Data: Q&A With HealthVerity 5/16/2023

    Director of Partners and Alliance Management at HealthVerity KC Ahlberg discusses some key trends related to the use of real-world data in clinical trials, and the value sponsors are realizing through data linkage.

  9. eConsent Readiness In 24 Countries 3/12/2024

    Discover how regulatory bodies worldwide, including the U.S. Food and Drug Administration and the European Medicines Agency, are now championing the shift towards eConsent adoption.

  10. A Dive Deep Into Castor's eConsent 11/16/2023

    Discover how digital consent is working to enhance diversity, empower participants with education, drive quality data, and streamline operations.