If your NIH RFA will involve collaborating sites, and NIH requires the use of a single IRB (“sIRB”), we remind you to consult with the Emory IRB very early on in the grant-writing process, and to not submit your sIRB plan without our prior review. We also remind you that reliance on an independent IRB is often the best solution, and this requires a quote and a line item in the study budget. Submit our special form to start the discussion: see “NIH Single IRB Policy” FAQ on our Collaborative Research webpage.
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Recent Articles for Emory’s Research Administrator
- NSF Updates (February 2023)
- NIH Updates (February 2023)
- RGC Exemption Request Form and Process Changes
- OCR Guidance for Creating Short Study Title
- Institutional Biosafety Committee
- RA Enterprise Systems and Processes
- PI Financial Portal
- RAS Support for PIs – Find Your RAS Contact
- Federal Agency Updates – NIH and NSF
- NIH Closeout Procedures (From the PI Perspective)
New from NIH
- NIH Clinical Trials Reporting Compliance: A Shared Commitment March 24, 2023To assess our progress with results information submission to ClinicalTrials.gov beyond 2020, we conducted analyses of NIH-grant-funded clinical trials for which main results were due in fiscal year (FY) 2020, FY 2021 or FY 2022.Mike Lauer
- NIH Clinical Trials Reporting Compliance: A Shared Commitment March 24, 2023
News from the Office of Technology Transfer
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