eConsent Resources

  1. 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.

  2. Unify Your Data With A Centralized eClinical Platform 3/12/2024

    Despite the challenges associated with large volumes of data, maintaining quality and regulatory compliance, and enhancing patient engagement, the solutions for managing them can be simple and efficient.

  3. How eConsent Improves The Trial Experience For Patients And Sites 4/5/2023

    In part one of this series, the author dives into how electronic consent platforms are simplifying and improving the trial experience for patients and sites.

  4. 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.

  5. What It Really Takes To Adopt eConsent Across Large Pharma 3/27/2024

    Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.

  6. 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.

  7. 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.

  8. Right-Size Your eConsent Approach 11/17/2023

    Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.

  9. Unlocking The Power Of Real-World Evidence In FDA Submissions 5/15/2023

    Understand the gaps between how data is collected in real-world evidence (RWE) and randomized clinical trials (RCT) and how RWE is quickly finding ways to catch up.

  10. Castor eConsent: Site View 8/21/2025

    Study coordinators aim to enroll participants efficiently through a partnership that leverages direct-to-patient marketing to streamline recruitment.