eConsent Resources

  1. The Revival Of Electronic Informed Consent 11/2/2022

    The clinical research industry has been reluctant to adopt eConsent for several reasons. Unearth how the industry should continue exploring and implementing digital technologies in earnest in the future.

  2. 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.

  3. A Dive Deep Into Castor's eConsent 11/16/2023

    Discover how digital consent is working to enhance diversity, empower participants with education, drive quality data, and streamline operations.

  4. eConsent For Complex Clinical Trials 10/31/2022

    Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk. Learn how a feature-rich eConsent platform can simplify those processes and improve engagement.

  5. Rare Disease Clinical Trials: Modern Design And Supply Chain 10/12/2023

    Gain insight from several contributing experts for overcoming unique obstacles in rare disease research and learn how to better develop strategies.

  6. EDC For Mid-Study Changes In Medical Device Clinical Trials 6/21/2022

    In this case study, discover how a company was pointed to an electronic data capture (EDC) system that was quick to adapt and easy to scale as the study changed.

  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. Simplify Clinical Trial Technology With An Emerging Aggregation Platform 7/24/2024

    Sites are frequently overwhelmed with the sheer number of technologies they must work with to conduct a clinical trial, and this aggregation platform can streamline trial management.

  9. 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.

  10. Evidence And Insights: Analysis On The Power Of Digital Trials 5/29/2024

    Digital and DCT elements like eCOA, platforms, and wearables have transformed the ways we conduct clinical research. Read through the latest industry analysis and data on the real impacts these technologies have on clinical trials with this new ebook.