Office of Regulatory Affairs

INSTITUTIONAL REVIEW BOARD (IRB)

• IRB Home
• MedStar Research Institute-Georgetown University Oncology IRB
• Social & Behavioral IRB
• IRB Board Members
• Contact Info
• Calendar of meetings
• IRB Forms
• IRB Manuals
• Human Subject Protection Training
• HIPAA Training
• Report Research Compliance Complaint or Concern
• Adverse Event Reporting
• IRB Fees
• Federal Wide Assurance (FWA)
  New! 01/29/2007

Biomedical IRB Forms (IRB-A, IRB-B)

Social and Behavioral IRB Forms (IRB-C)

MedStar Research Institute (MRI) - Georgetown University (GU) Oncology IRB Forms (IRB-D)

Templates for Informed Consent, Non-English Speaking Subjects

Study Specific Disclosure Form
(NEW 01/02/2008)

HIPAA Forms

Adverse Event Report Forms (IRB-A, IRB-B, IRB-C, IRB-D)

Computerized Adverse Event Reporting (CAER). Please note: you must be an authorized user to access this system. If you are a new coordinator and have not gone through the CAER orientation, please send an email to caer@georgetown.edu to schedule a training.

Radiation Safety Committee Forms

Quick Links:

• Clinical Trials Office
• Sponsored Programs
• University Counsel
• Internal Audit
• HIPAA Information for Researchers
• Georgetown University Financial Conflicts of Interest Policy
• Lombardi Comprehensive Cancer Center
• General Clinical Research Center (GCRC)
• Exempt Research
• Office of Compliance and Ethics
• Registration of Clinical Trials