eConsent Resources

31. Virtual eConsent For Decentralized Trials 12/23/2025

    Virtual eConsent improves accessibility and compliance in decentralized trials, streamlining enrollment with a secure, user-friendly process for informed consent in remote research.

32. Using eConsent Data To Populate Site And Sponsor Data Systems 10/7/2024

    A top-10 pharmaceutical company was looking to reduce the amount of administrative burden on their clinical trial sites and themselves. See how we accomplished it, using eConsent.

33. eConsent For Complex Clinical Trials 10/31/2022

    Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk. Learn how a feature-rich eConsent platform can simplify those processes and improve engagement.

34. Introducing Digitally-Enabled Biosample Consent Storage 6/13/2024

    Despite the rise of digital solutions in healthcare, paper consent forms are still common in today’s clinical trials. Unfortunately, these paper forms pose significant challenges in retaining the documentation of informed consent for centrally stored biospecimens.

35. Work Flow Walk Through: eConsent Platform 2/28/2023

    Within DSG’s unified system, e-consent is simple. Witness how teams can easily and efficiently register participants for clinical trials.

36. EDC For Mid-Study Changes In Medical Device Clinical Trials 6/21/2022

    In this case study, discover how a company was pointed to an electronic data capture (EDC) system that was quick to adapt and easy to scale as the study changed.

37. 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.

38. How To Make eConsent Accessible Across Diverse Populations 3/30/2026

    Accessible eConsent removes language, literacy, disability, and tech barriers, improving comprehension, equity, compliance, participant trust, inclusive enrollment, and data quality.

39. 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.

40. Addressing Site And Sponsor Challenges In Digital Trials 10/10/2023

    <p>While the digital transformation of clinical trials has made tremendous strides in recent years, the plethora of new technologies can overwhelm. Learn how to help sites and sponsors combat the overload of technology.</p>