eConsent Resources

  1. Technology Overload: Addressing Site Challenges Of Digital Trials 5/23/2024

    Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.

  2. 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.

  3. Designed To Help Sites Increase Clinical Trial Capacity 7/25/2025

    IQVIA One Home for Sites is a platform that serves as a neutral aggregator, connector, and communicator of the key systems and tasks a clinical research site needs to perform across all the trials it is conducting.

  4. 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. 

  5. How Heron Therapeutics Sped Up Database Creation 12/2/2022

    Electronic data capture (EDC) is straightforward, in theory. However, not every EDC is purpose-designed for ease of use by study teams, and some are easier to use and more intuitive than others.

  6. 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.

  7. How eConsent Primes Patients And Studies For Success 9/14/2022

    Understand how the informed consent process ensures trial participants are adequately educated about the trial and what's required of them during the process while confirming their willingness to enroll.

  8. 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.

  9. 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.

  10. The New Era Of Evidence Generation In Clinical Trials 6/19/2024

    Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.