23 Sep POSTPONED — A Single IRB: The Promise and the Reality
UPDATE: EVENT POSTPONED
The March 11, 2020 Clinical Research Education Series (CRES) webinar offering on A Single IRB has been postponed. We will be back in touch to inform you of the new date once confirmed. Please feel free to contact Aric Lane with questions.
Single IRB (sIRB) review is now mandated for most federally-funded research involving human subjects. The policy requires the use of one IRB to accomplish IRB review and approval for all domestic sites. The goal of this requirement is to enhance and streamline the IRB review process for multi-site research so that research can proceed as quickly as possible without compromising ethical principles and protections for human research participants. Implementing this policy will require IRBs and investigators to significantly rethink and restructure their processes for multi-site research.
This session will discuss the different sIRB policies, how they impact investigators at the time they are writing grants and after the grant is funded, changes IRBs are making to implement single IRB review, and the resources investigators and their teams will need to successfully manage a multi-site study under single IRB review.
Schedule of activities
- 11:30-11:45 – registration and lunch
- 11:45-11:50 – welcome and intro
- 11:50-1:05 – presentation, interactivity, Q&A
- 1:05-1:15 – thank you and feedback survey
By the end of this session, you will be able to:
- Understand what single IRB review is
- Recognize what kinds of studies must comply
- Explain the overall process for obtaining single IRB review
- Plan for single IRB review for a multi-site research study
About the speaker
Adrienne Meyer, MPA, CIP, is the Assistant Director of Reliances in the Human Subjects Division at the University of Washington (UW). Adrienne is a regulatory specialist and frequent lecturer on issues associated with regulatory compliance and research ethics in a broad spectrum of research disciplines. Adrienne has been at the UW for nearly 20 years and has worked in many capacities with researchers from nearly every department and research discipline: from behavioral research with young children to first-in-human chemotherapy trials. She is the SMART IRB Ambassador for the West and Pacific region and the IRB representative on ITHS’s Trial Innovation Network team.
This meeting will be online only. Please register to receive the Zoom link. If you previously registered to attend in-person, the Zoom link will be sent to you before the event.
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