Transitioning Research to the Revised Common Rule: The What, How, and Why
Learn about considerations and challenges for transitioning pre-existing research to the revised Common Rule, as well as required documentation and tips for IRB review.
About this Webinar
View this webinar and learn about the applicability of the pre-2018 and 2018 versions of the Common Rule, the factors an organization may want to consider when deciding whether to transition a pre-existing study (or studies) to comply with the revised Common Rule, and strategies for the management and communication of transition decisions.
Language Availability: English
Suggested Audiences: Researchers, Research Team Members, Institutional Review Boards (IRBs), Institutional/Signatory Officials, 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
Webinar Content
Transitioning Research to the Revised Common Rule: The What, How, and Why
Presented by: Karen Christianson, RN, BSN - HRP Consulting Group
This webinar reviews the pre-2018 and 2018 versions of the Common Rule, factors an organization may want to consider when deciding whether to transition a pre-existing study (or studies) to comply with the revised Common Rule, and strategies for the management and communication of transition decisions.
Recommended Use: Required
ID (Language): 19592 (English)