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Non Georgetown Researchers
If you are an investigator located at another MedStar hospital and wish to enroll patients into your trial at Georgetown University Hospital, you must:
- Complete a Georgetown University,(GU) IRB application
- If you haven't already done so, complete a MedStar-GU joint consent form if you intend to enroll at GUH and at other MedStar facilities
- Complete a GU consent form if you only intend to enroll at GUH
- Submit the application and consent form to the GU IRB. For exact submission requirements and an IRB review schedule, click here
- Note that if your trial is an Oncology Trial, you should make use of the central GU-MedStar Oncology IRB. Information about the use of this IRB can be obtained from Laura Miller at 202-687-1506
- Contact Trudy Bright (Assistant Director, Georgetown University, Office of Sponsored Research) at 202-687-1227 to determine what contracting requirements will be required for your study
- Provide a copy of your study protocol to the Clinical Trials Office for cost analysis related to conducting the study at Georgetown University Hospital
- Refer to the "What other departments might I need to contact prior to beginning enrollment?" section of the New Trial Startup section
For any questions concerning this process, please contact the CTO at 202-444-5838.
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