eConsent Resources

  1. Going Global With eConsent 4/20/2022

    Scott Askin paints the picture of why Novartis, determined to improve the patient experience, has begun to deploy eConsent, and what they’ve learned along the way.

  2. How eConsent Primes Patients And Studies For Success 9/14/2022

    Understand how the informed consent process ensures trial participants are adequately educated about the trial and what's required of them during the process while confirming their willingness to enroll.

  3. Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study 12/20/2024

    This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.

  4. Deploy eConsent Around The World With Confidence 8/16/2022

    Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.

  5. Agile eConsent: Taking A Flexible Approach To Global Implementation 6/28/2022

    Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.

  6. Work Flow Walk Through: eConsent Platform 2/28/2023

    Within DSG’s unified system, e-consent is simple. Witness how teams can easily and efficiently register participants for clinical trials.

  7. Headed Down Registry Road? Here Are The EDC Features You'll Need 3/18/2022

    Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.

  8. 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.

  9. 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.

  10. Unify Your Data With A Centralized eClinical Platform 3/12/2024

    Despite the challenges associated with large volumes of data, maintaining quality and regulatory compliance, and enhancing patient engagement, the solutions for managing them can be simple and efficient.