This webinar discusses the informed consent requirements related to increasing understandability of information to support good decision-making. It includes language and organizational tips, and suggestions for how to meet the ”key information” requirements of the revised Common Rule using practical examples and examining different types of studies.
Language Availability: English
Suggested Audiences: Researchers, Research Team Members, Institutional Review Boards (IRBs), IRB Chairs, IRB Administrators and Staff, Human Subject Protection Staff, Students
Organizational Subscription Price: $300 per year/per site or included as part of the $1,000 annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person
Understanding Consent Requirements and “Key Information” Under the Revised Rule
Presented by: Misti Ault Anderson, MS, MA – HHS Office for Human Research Protections
This webinar provides learners with a review of the new regulatory requirements for understandability in informed consent documents. During the webinar, learners will explore ways to develop consent materials that reflect what potential participants need to know and understand in order to make autonomous decisions about whether to participate in research, with particular emphasis on the new “key information” requirements of the revised Common Rule. This webinar is ideal for individuals preparing consent materials for new research, as well as IRB members and staff who review consent forms or provide support to researchers at their organizations.
Recommended Use: Required
ID (Language): 19970 (English)