eConsent Resources

  1. Supporting Early Phase Oncology Research With The Right Data Management System 3/15/2024

    Better understand how the evolving landscape drives innovation, why your data capture strategy needs the right technology foundation, and what to look for in a CDMS/EDC system for early-phase oncology.

  2. 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.

  3. Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study 12/20/2024

    This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.

  4. 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.

  5. Re-Consent In Clinical Trials: Streamlining With eConsent 11/29/2023

    Delve into a variety of triggers for initiating re-consent, perspectives of regulators and IRBs regarding the re-consent process, and the role of digital processes in preventing issues related to re-consent.

  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. Agile eConsent: Taking A Flexible Approach To Global Implementation 6/28/2022

    Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.

  8. Simplify Clinical Trials With Signant SmartSignals® Unified Platform 8/16/2024

    Signant SmartSignals® Unified Platform streamlines clinical trials by integrating eConsent, data collection, remote consultations, and randomization, simplifying workflows for patients and site staff.

  9. Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations 2/22/2023

    Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

  10. 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.