eConsent Resources

  1. What Is Electronic Data Capture And How Does It Simplify Data Management? 5/6/2025

    As EDC systems continue to evolve, they streamline workflows, enhance data security, and improve patient outcomes.

  2. Revolutionizing Pediatric Clinical Trials With ePRO And eConsent 10/16/2024

    Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.

  3. Designing ePRO And eConsent For Pediatric Trials 8/29/2024

    Gain confidence in making your next pediatric trial more successful by leveraging the technology discussed to address common challenges in pediatric studies.

  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. Biosample Tracking: A Consenting Dilemma 3/7/2023

    Biosample collection is an inevitable part of most clinical trials. Learn how sponsors should be tracking every sample back to the source so as to not violate compliance issues.

  6. Designed To Help Sites Increase Clinical Trial Capacity 7/25/2025

    IQVIA One Home for Sites is a platform that serves as a neutral aggregator, connector, and communicator of the key systems and tasks a clinical research site needs to perform across all the trials it is conducting.

  7. 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.

  8. Unlocking The Power Of Real-World Evidence In FDA Submissions 5/15/2023

    Understand the gaps between how data is collected in real-world evidence (RWE) and randomized clinical trials (RCT) and how RWE is quickly finding ways to catch up.

  9. How eConsent Can Help Legally Authorized Representatives 6/22/2022

    Software vendors often forget to think about the needs of LARs, even though they play a vital role in clinical trials. Explore three ways eConsent can help LARs complete the informed consent process.

  10. 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.