eConsent Resources

  1. The Catch-22 Of eConsent: A Missed Opportunity For Improved Trials 3/21/2025

    Drawing on evidence from scientific literature, we examine the pitfalls that have hindered its success and propose actionable solutions to unlock its true value in clinical research.

  2. Castor eConsent: Site View 8/21/2025

    Study coordinators aim to enroll participants efficiently through a partnership that leverages direct-to-patient marketing to streamline recruitment.

  3. Revolutionizing Pediatric Clinical Trials With ePRO And eConsent 10/16/2024

    Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.

  4. How To Prepare An IRB Submission For A Remote eConsent Study 1/24/2022

    IRBs are increasingly supportive of eConsent solution. Even so, researchers may find themselves in need of guidance as they prepare for an eConsent IRB review.

  5. 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.

  6. 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.

  7. Bridging Clinical Efficacy And Real-World Effectiveness In Digital Therapeutics Trials 2/7/2022

    No matter how conclusive clinical evidence is for medical treatments, developers may struggle to see precisely how their treatment performs in the real world—outside the controlled environment of the clinic or office.

  8. The Impact Of An AI Enabled Consent Process 5/15/2024

    In this episode of Download with Derk, we take an in-depth look at our internal experiment where Castor Companion was utilized during the consent process.

  9. Biosample Tracking: A Consenting Dilemma 3/7/2023

    Biosample collection is an inevitable part of most clinical trials. Learn how sponsors should be tracking every sample back to the source so as to not violate compliance issues.

  10. Comparative Effectiveness Of eConsent: Systematic Review 4/17/2024

    This blog post examines eConsent vs. ICF on comprehension, acceptability, enrollment, retention, consent time, and site workload.