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.

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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:

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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)