eConsent Resources

  1. 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.

  2. 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.

  3. 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.

  4. Seamless And Integrated Onboarding For Trial Participants 10/23/2024

    Streamline your patient experience with a comprehensive, all-in-one solution that allows you to recruit, screen, and enroll participants remotely from the comfort of their own homes.

  5. 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.

  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. EU Annex 11: How To Stay Compliant 11/16/2022

    EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Learn how sponsors and sites seeking treatment approval in the EU must follow Annex 11. 

  8. 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.

  9. A Data-Driven Exploration Of Decentralized Elements, Digital Tech 6/13/2024

    Discover how Medable and industry leaders are accelerating clinical research and transforming patient care in the era of digital innovation.

  10. 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.