Webinar | May 18, 2018

How eConsent Optimizes Research For Sponsors And CROs

Source: Quorum Review IRB

Get CEUs through Webinar On-Demand

Electronic informed consent, or eConsent, is an exciting potential tool for clinical researchers. But why should they adopt it? Will it positively impact timelines? Will it complicate research?

Discover how the right eConsent tool will pay dividends by delivering real-world efficiency and improved compliance. Plus, get tips for choosing an eConsent vendor that will help you successfully transition away from paper.

Those who attend this 60-minute webinar will:

  • Find out how to streamline study startup time with the right eConsent tool and vendor
  • Discover ways eConsent can prevent consenting errors the first time
  • Learn how the right eConsent tool directly connects to participant engagement and retention