HRA INFORMED CONSENT INCLUDING ECONSENT FOR HUMAN SUBJECTS RESEARCH
COURSE REGISTRATION

Registration for both the live webinar and the pre-recorded on-demand courses is available in HealthStream.  Search for “HRA Informed Consent including eConsent for Human Subjects Research”

COURSE DESCRIPTION

This course is for investigators and all members of the study staff.  Course content is based on Good Clinical Practice Guidelines, federal and state research regulations, and institutional research policies.  Although many research teams require this comprehensive informed consent course as part of onboarding, it is also a great refresher for experienced members of the study team to ensure they are aware of the most current research regulations, institutional policies, and best practices for consenting human subjects.  The course includes information on:

  • Informed Consent Requirements
  • Vulnerable Populations and Special Circumstances
  • Types of Consent and Consent Processes
  • Common Consent Compliance Issues
COURSE FORMAT OPTIONS
  • In-person, instructor led live webinar training – Eligible for RCR Credit!
  • Pre-recorded course available on-demand
COURSE LENGTH

The course takes 1 ½ hours to complete

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