JUNE 12, 2014 TO JUNE 13, 2014
CTTI Project: Single IRB
Meeting Objectives:
- Discuss practices, implementation strategies, and solicit additional suggestions for increasing the use of central IRBs for multi-center clinical trials
- Present findings from the CTTI Central IRB Advancement project’s collection of IRB authorization agreements and standard operating procedures
- Obtain additional feedback to refine proposed IAA template and tools
Meeting Location:
Hilton Washington DC/Rockville Executive Meeting Center, Rockville, MD
Meeting Presentations:
DAY 1 – JUNE 12 , 2014
- Welcoming Remarks by Bray Patrick-Lake
- Landscape of the Use of Central Institutional Review Boards for Multi-center Clinical Trials by Soo Bang
- Academic Institution Example: Reliance on Independent IRBs for Multi-center Clinical Trials by David Borasky
- Federal Central IRB Example: The NCI CIRB Initiative by Jacquelyn Goldberg
- Industry Sponsor Example: Sponsor’s Experience - Challenges of Implementation by Soo Bang
- IRB Authorization Agreement Data Collection by Cynthia Hahn
The views and opinions expressed in this presentation are those of the individual presenter and should not be attributed to the Clinical Trials Transformation Initiative, or any organization with which the presenter is employed or affiliated.