eConsent Resources

  1. Successful Subject Creation With eCOA, eConsent, & IRT Process Flow 5/26/2023

    Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.

  2. Combining Patient-Centric Technology and RWD For Comprehensive Evidence 8/10/2022

    Explore how by combining digital technologies with secondary RWD, researchers can gather a more holistic understanding of the patient. 

  3. Introducing Digitally-Enabled Biosample Consent Storage 6/13/2024

    Despite the rise of digital solutions in healthcare, paper consent forms are still common in today’s clinical trials. Unfortunately, these paper forms pose significant challenges in retaining the documentation of informed consent for centrally stored biospecimens.

  4. 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.

  5. 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.

  6. Minimizing Hurdles For Patients During The eConsent Process 10/4/2022

    Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.

  7. A Definitive Guide To Evidence Generation 10/18/2023

    Obtain a complete understanding of enrollment, screening, consent, and data collection by diving into this introductory handbook on decentralized clinical trials.

  8. Protocol Amendments And Electronic Consent: Overcoming The Challenges To Reap The Benefits 3/29/2022

    Learn about some insights that have been gleaned from experience deploying eConsent on diverse trial types around the world.

  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. EU Annex 11: How To Stay Compliant 11/16/2022

    EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Learn how sponsors and sites seeking treatment approval in the EU must follow Annex 11.