eConsent Resources

  1. Better eConsent Through Education Best Practices 9/23/2022

    eConsent can have a positive impact on participant retention, but learn why that is only part of the challenge of meeting participant needs in a clinical trial.

  2. Efficiently Manage Clinical Data With Castor's EDC, CDMS 5/11/2023

    Effortlessly conduct multi-center clinical trials worldwide for drug development with Castor’s EDC and CDMS platforms, including eCOA, ePRO, EHR eSource, eConsent, and IRT modules.

  3. 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.

  4. 10 FAQs On eConsent 11/16/2023

    Closely examine the challenges of adoption, integration, and compliance measures involving eConsent and gain valuable insights for those contemplating their incorporation in clinical trials.

  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. A Better Approach To eConsent: Flexibility With Enabled Technology 1/11/2023

    Electronic consent, or eConsent, digitalizes the trial participant consent process through increasingly simplified, interactive, educational models designed to improve comprehension and boost engagement.

  7. Digital Versus Digitized: Common Misconceptions About eConsent 7/27/2022

    In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.

  8. 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.

  9. Using eConsent Data To Populate Site And Sponsor Data Systems 10/7/2024

    A top-10 pharmaceutical company was looking to reduce the amount of administrative burden on their clinical trial sites and themselves. See how we accomplished it, using eConsent.

  10. Increase Participant Diversity With eClinical Tools 4/14/2023

    The right technology and community partnerships can help sponsors meet FDA diversity requirements without additional expenditures, build relationships with minorities, and prepare for future trials.