eConsent Resources

1. 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.

2. 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.

3. Preparing Studies With eConsent For IRB Approval 6/7/2023

   Understand how eConsent can benefit trials and align with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models.

4. Unleash The Power Of IQVIA Complete Consent 11/12/2024

   Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.

5. Building One Home for Sites 7/23/2024

   Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.

6. 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.

7. 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.

8. 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.

9. 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.

10. 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.