Investigator Guidance Documents and IRB Policies/SOPs
The George Washington University Investigator Guidance and IRB Policies and Procedures
IRB Basics for GW Researchers
Current Investigator Guidance
- Investigator Obligations (HRP-800)
- Prompt Reporting Requirements (HRP-801)
- Informed Consent (HRP-802)
- Documentation of Informed Consent (HRP-803)
- Human Subjects Protections Training (HRP-804)
- Study Expiration (HRP-805)
- Study Closure (HRP-806)
- Submission Requirements (PDF)
- Classroom Research (HRP-808)
- Adults Lacking Capacity to Consent (HRP-809)
- Legally Authorized Representative Identification Template Form (HRP-582)
- Additional DOD Obligations (HRP-810)
- Additional DOE Obligations (HRP-811)
- Additional DOJ Obligations (HRP-812)
- Additional ED Obligations (HRP-813)
- Additional EPA Obligations (HRP-814)
- Additional FDA Obligations (HRP-815)
- Additional ICH-GCP Obligations (HRP-816)
- Student Initiated Research (HRP-817)
- Blood Draws (PDF)
- Chart Reviews (PDF)
- International Research (PDF)
- Explanation of Limited IRB Review (PDF)
- Version Control for Study Documents (PDF)
- What is the "Key Information" Section in the Informed Consent Form? (PDF)
Policies and Procedures
- Definitions (HRP-001)
- Abbreviations (HRP-002)
- Designations (HRP-003)
- Human Research Protection Program (HRP-010)
- Principal Investigators (HRP-011)
- IRB Member Review Expectations (HRP-020)
- Legally Authorized Representatives, Children, and Guardians (HRP-021)
- End Approval Dates (HRP-022)
- IRB Records (HRP-023)
- IRB Roster (HRP-024)
- States and Transitions (HRP-050)
- IRB Member Review Expectations HUD (HRP-080)
- Pharmacists as IRB Members (HRP-081)