eConsent Resources

1. End-To-End Clinical Data Flow 6/24/2024

   Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.

2. eConsent – The Enrollment Solution For Decentralized Trials 2/1/2022

   The COVID-19 pandemic and the increased technological competence required to enroll and retain research participants has left many organizations wondering how to modernize their enrollment and consent process. Find out more about the landscape and its impact in the available webinar.

3. Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations 2/22/2023

   Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

4. 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.

5. The Building Blocks Of DCT: How To Create A Seamless Experience Across eConsent, eCOA, And More 3/29/2022

   With more than 76% of sponsors seeking to implement decentralized solutions this year, there’s never been more attention given to decentralized trials. Discover why decentralized trials must take a unified approach, one that alleviates burdens for patients and sites in order to drive cost savings and realize efficiencies. 

6. Patient Perspectives On eConsent 12/20/2023

   Explore how eConsent enables participants to engage meaningfully with consent documentation, addressing information dissemination, explanation, and recall challenges.

7. 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.

8. 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.

9. eSource Enables Speed, Flexibility, And Higher-Quality Data 7/22/2022

   A truly integrated eSource Solution, including DDC, eCOA, and eConsent, facilitates remote or decentralized clinical trials by ingesting data from multiple sources and consolidating it into a single data set.

10. 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.