eConsent Resources

1. 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.

2. Effortless Hybrid Consent 2/22/2022

   Watch this webinar to see the latest eConsent workflow from recruitment, to pre-screening, to remote consent.

3. How To Prepare An IRB Submission For A Remote eConsent Study 1/24/2022

   IRBs are increasingly supportive of eConsent solution. Even so, researchers may find themselves in need of guidance as they prepare for an eConsent IRB review.

4. Navigating Successful eConsent Adoption From Sponsor To Site 10/17/2023

   Drawing inspiration from real-world instances within the pharmaceutical and medical device sectors, watch as industry experts unravel the pivotal role of eConsent in optimizing modern clinical trials.

5. 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.

6. 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.

7. 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.

8. 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.

9. How Capturing Data Directly Is Transforming Trials 2/3/2023

   With the right eSource technology, discover how trial data can be aggregated, integrated, and classified to accelerate data analysis for insight-based decisions in real time.

10. Study Start-Up Checklist For Digital Clinical Trials

    Read how five Florence employees with clinical research backgrounds came together to craft a checklist designed to walk sites through the process of tech-enabled study start-up.