Use of eConsent: A Look at the Regulatory Guidance

Event Date: 

Wed, Feb 17, 2021 - 10:00am to 11:00am


This presentation will focus on the regulatory requirements for the use of electronic consent (eConsent).  Attendees can expect to learn more about

  • The Office of Human Research Protection (OHRP) & The Food and Drug Administration (FDA) shared guidance on “Use of Electronic Informed Consent in Clinical Investigations – Questions and Answers”
  • UI tools for researchers setting up an electronic consent (eConsent) process
  • What to expect when using an external eConsent tool for FDA regulated research


Pre-registration is recommended.