If a research study meets any one of the following definitions, the trial must be registered on ClinicalTrials.gov: The Food and Drug Administration (FDA) requires registration for “applicable clinical trials” (ACTs) defined as follows: For any trials of drugs and biologics: controlled clinical investigations, other than Phase I investigations, of a product subject to FDA […]
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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
- Data Management and Sharing Plan vs. Resource Sharing Plan March 20, 2023The Data Management and Sharing (DMS) Plan and Resource Sharing Plan are separate attachments that may be required for your application. One does not necessarily replace the other. Read on to learn more.NIH Staff
- Data Management and Sharing Plan vs. Resource Sharing Plan March 20, 2023
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