eConsent Resources

1. The Impact Of An AI Enabled Consent Process 5/15/2024

   In this episode of Download with Derk, we take an in-depth look at our internal experiment where Castor Companion was utilized during the consent process.

2. Site Tech, Integration, And Reducing Burden 6/12/2026

   Beth Harper, Rosie Filling, and Joe Dustin discuss site tech, integration, and how sponsors can reduce burden while improving flow.

3. 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.  

4. Simplify Clinical Trials With Signant SmartSignals® Unified Platform 8/16/2024

   Signant SmartSignals® Unified Platform streamlines clinical trials by integrating eConsent, data collection, remote consultations, and randomization, simplifying workflows for patients and site staff.

5. 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.

6. Ask Sites What Technology They Already Use 6/12/2026

   Rosie Filling says sponsors should stop guessing and ask sites what tech they use so teams can design with sites, not just for them.

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. Qualified eSignature in Electronic Consent Systems 2/25/2026

   This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.

9. How eConsent Is Changing The Informed Consent Process 5/26/2022

   Learn how informed consent — providing a potential participant with enough information about a study to allow for an informed decision about their participation — is a critical step for enrolling patients in clinical trials.

10. ePROs: How They're Transforming Oncology Research 10/30/2023

    ePRO and eCOA are helping to overcome oncology-specific challenges in clinical research. Find out how you can make life easier for patients when it matters most.