eConsent Resources

  1. 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.

  2. 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.

  3. Medrio eConsent 10/25/2023

    Support the digitization of the participant consent process and begin creating multimedia-enhanced electronic informed consent forms (eICFs) that participants sign electronically, eliminating burdensome and error-prone paper-based processes.

  4. Addressing The Specific Complexities Of Oncology eCOA Clinical Trials 4/18/2022

    What are the specific tools and keys to conduct eCOA trials in oncology successfully? This article identifies some of the relevant solutions to tackle oncology protocol complexities.

  5. Digital Versus Digitized: Common Misconceptions About eConsent 7/27/2022

    In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.

  6. 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.

  7. Tips For Tailoring eConsent For Optimal Patient Centricity 3/29/2022

    While informed consent is a critical process for ensuring participant autonomy, consent forms are too long, unclear, difficult to read, and frequently exceed 9th grade reading levels. Explore why eConsent is a potential solution to this problem.

  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. 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 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.