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eConsent in Action - How It Works and Why Patients Appreciate It

March 28, 2019

As sponsors and CROs continue to prioritize patient centricity in clinical trials, it is little surprise that eConsent has become a driving topic in every conference agenda. In addition to providing a warm and welcoming introduction to the trial, eConsent has consistently demonstrated the ability to improve patient satisfaction, reduce consent-related protocol deviations and support higher retention rates.

Still, common questions remain such as…

  • Can I afford it?
  • What is the measured ROI?
  • How does it change the ICF creation process?
  • Does it work globally?

Watch this 45-minute webinar where we discuss benefits for patients, sites and study teams, address common questions and concerns, and present a brief technology demonstration to help you make eConsent decisions for your upcoming trials.

Previous Video
Enabling Electronic Informed Consent for Clinical Research Sites
Enabling Electronic Informed Consent for Clinical Research Sites

Watch this information session on electronic informed consent designed exclusively for clinical research si...

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Optimizing eConsent for Patient Centricity
Optimizing eConsent for Patient Centricity

Experts from across the clinical trial industry share their data, real case studies and expertise on how to...