Is Your Site Ready for eConsent?

Society for Clinical Research Sites (SCRS) Webinar

Date: July 17, 2018 @ 9:00 am PT | 12:00 pm ET

Is your site eConsent ready? As more study sponsors prefer to work with sites that are familiar and engaged with electronic informed consent (eIC) forms and solutions, this webinar will focus on best practices that ensure compliance and operational inefficiencies. Find out how to prepare your site to be ready regardless of the eConsent solution or vendor.

Webinar attendees from sites will gain the following key takeaways:

  • Identify gaps in policy, procedures, and compliance;
  • Prepare your clinical operations teams to understand eConsent technologies, regulations, and how IRBs review eIC systems and forms;
  • Learn what types of SOPs and procedural templates are helpful;
  • Discover how eIC can help to improve patient retention and recruitment.




Presented by: James Riddle, MCSE, CIP, CPIA, CRQM

James RiddleJames is VP of Client Services at Kinetiq. He previously worked as Assistant Director at the Fred Hutchinson Cancer Research Center and has over 15 years of experience leading private and academic human subject protection programs. He has been a site visitor for AAHRPP, is a faculty member, mentor, and regular speaker for Public Responsibility in Medicine and Research. James served on the Board of the Northwest Association for Biomedical Research, and is a Certified IRB and IACUC Professional.

eConsent Webinar

Register to watch the webinar via SCRS

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