eConsent Resources

1. Linking Clinical Trial Data With Real-World Data: Q&A With HealthVerity 5/16/2023

   Director of Partners and Alliance Management at HealthVerity KC Ahlberg discusses some key trends related to the use of real-world data in clinical trials, and the value sponsors are realizing through data linkage.

2. Technology Overload: Addressing Site Challenges Of Digital Trials 5/23/2024

   Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.

3. The Definitive Guide To Decentralized Clinical Trials 6/8/2023

   See how the clinical trial landscape has changed, and why many sponsors are choosing to make digital and decentralized trials a key part of their future.

4. 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.  

5. Addressing Site And Sponsor Challenges In Digital Trials 10/10/2023

   <p>While the digital transformation of clinical trials has made tremendous strides in recent years, the plethora of new technologies can overwhelm. Learn how to help sites and sponsors combat the overload of technology.</p>

6. Oncology Preferences From Patients And Caregivers On Trial Tech 6/14/2023

   Delve into the preferences of patients and caregivers in the field of oncology, specifically regarding eConsent, telehealth, wearables, and other digital technologies.

7. Digital Medicine Society Accelerates Recruitment and Results With eConsent 9/26/2022

   Find out how the Digital Medicine Society (DiMe), an interdisciplinary professional society for digital medicine, was able to deploy an eConsent module in less than two weeks to support its remote study to assess nocturnal scratching as an endpoint for patients.

8. 3 Proven eConsent Implementation And Adoption Best Practices 1/19/2024

   By advocating these three essential best practices, learn how stakeholders can navigate the complexities of eConsent adoption with confidence and enhance the overall efficiency and success of clinical trials.

9. The Win-Win Wth Virtual Visits – Better Experiences, Better Data 2/29/2024

   Discover how researchers can design studies with the needs of the patient in mind to promote faster enrollment, high engagement, and the production of more complete and accurate data.

10. Discover Why Electronic Revisions Of ICFs Are Easier 10/7/2024

    What does the ICF amendment or revision process look like within a digital platform and is this harder or easier than traditional paper-based approaches?