Free Webinar
Adopting eConsent in Research: Security, Privacy, and Regulatory Considerations

eConsent adoption is on the rise, and with that comes a heightened focus on the compliance of eConsent platforms and the protection of data. This webinar will walk through the security and privacy requirements related to eConsent, as well as other compliance considerations for sponsors, CROs, research sites, and IRBs. Specifically, attendees will learn the practical impact of:

  • 21 CFR Part 11 (Part 11)
  • The HIPAA Privacy and Security Rules
  • FDA Guidance on eConsent
  • Little-Known Other Requirements Related to eConsent

Mitchell Parrish, JD, RAC, CIP
VP of Legal & Regulatory Affairs, Kinetiq
The Technology and Consulting Division of Quorum Review IRB

Free Webinar Registration

Who Should Watch

Executives, directors, and managers who work for sponsors, CROs, research sites and IRBs. Also, members of these organizations who are charged with ensuring compliance amidst the proliferation of research technology.

CEU Credits

This webinar is pre-approved for 1.0 contact hours of continuing education credit for the Certified IRB Professional (CIP) certification, and for Maintenance of ACRP's CCRC®, CCRA®, CCTI® or CPI® certifications. If you are interested in another certification, please contact your professional organization to ask if this webinar meets their certification requirements.

Certificate of Attendance

After completing this webinar and the survey at the end, a certificate of attendance will be emailed to you. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete survey at the end. Visit our help page for more information on certificates of attendance.