eConsent Resources

  1. 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.

  2. Putting Power Back In The Hands Of Patients 11/21/2022

    Empower your patients throughout the clinical trial journey and eliminate the barriers and friction that get in their way with YPrime's eConsent platform.

  3. 7 Key Findings From A Clinical Trial Operations Technology Survey 1/19/2022

    To stay competitive in the clinical research field, sites, sponsors, and CROs need to invest in remote technology. Discover seven key trends that your clinical trial team needs to know about.

  4. Waiver Of Consent vs Waiver Of Written Consent 11/21/2024

    Learn the distinctions between a Waiver of Consent and a Waiver of Written Consent in clinical trials, and the importance of informed consent, particularly in the context of virtual trials.

  5. 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. 

  6. Pharmaceutical Company Gets Unified Decentralized Platform 2/28/2023

    Unearth how this global eClinical provider delivered a decentralized platform including eSource/ePRO for direct-data-entry, randomization, eConsent, telehealth, remote monitoring, and data management.

  7. Qualified eSignature in Electronic Consent Systems 2/25/2026

    This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.

  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. New Duke Research Shows Participants Prefer Enhanced eConsent 10/7/2024

    It’s apparent to those who have used it that the “e” in eConsent could stand for much more than 'electronic'. Duke’s new research shows why participants prefer an eConsent experience bolstered with videos, media, questions, and more.

  10. 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.