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.

Questions? Contact Us
Scroll Down Arrow


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.

Webinar Demo:

View Series Page for FAQs

Release Date: April 1, 2019

Language Availability: English

Suggested Audiences: Human Subject Protection Staff, Institutional Review Boards (IRBs), Institutional/Signatory Officials, IRB Administrators and Staff, IRB Chairs, Research Team Members, Researchers, Students

Organizational Subscription Price: $300 per year/per site or included as part of an 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)


Learn More

Your Name(Required)
I'd Like To Receive Emails From CITI Program
This field is for validation purposes and should be left unchanged.