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
