This webinar reviews ethical principles, discusses regulatory requirements for informed consent, and offers strategies to develop high-quality, participant-centered informed consent documents and discussions.
Note: This webinar is part of the OHRP webinars on 45 CFR 46. It is also available at no charge at https://www.hhs.gov/ohrp/education-and-outreach/human-research-protection-training/ohrp-webinars-on-45-cfr-46/index.html.
Original Recording Date: March 30, 2023
Release Date: May 29, 2025
Language Availability: English
Suggested Audiences: Grant Reviewers, Human Subject Protection Staff, Institutional Leadership, IRB Administrators, IRB Members, Research Personnel, Researchers, Students
Organizational Subscription Price: Included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: N/A
