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
  • Biomedical (IRB-A,B)
  • Social & Behavioral (IRB-C)
  • MRI-GU Oncology (IRB-D)
• 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

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

To apply for Full Board approval for new studies, please use the new web based electronic application system called eRIC. D-1 paper forms are no longer accepted for Full Board Initial Review For information on eRIC please contact Alex Mihai, IT Specialist for the Department of Regulatory Affairs
Educational Research Is IRB review required?
IRB Forms and Cover Letters
MRI-GU Application for Oncology IRB Review. (D-1) Please use for expedited applications only MRI-GU Continuing Review Form (D-2) MRI-GU Request for Expedited Oncology IRB Review (D-3) MRI-GU Request for IRB Review Exemption (D-4) Central IRB Application Form (D-5) Amendment Cover Letter Network Form (D-6)
Informed Consent From Templates and Guidelines
Joint MRI-GU Informed Consent Template Updated 11 August 2009 Required elements of a consent form Code of Federal Regulations Title 45 Public Welfare Department of Health And Human Services Part 46 Protection of Human Subjects 46.116 General requrements for informed consent 46.117 Documentation of informed consent GU-Merck Informed Consent Template Treatment Guidelines for Completing an Informed Consent Form Glossaries of Lay Terms Glossary of Lay Terms (medical terms in lay language, from Stanford) Lay Language for Medical Terms (University of Kentucky) Lay Terminology (North Shore Long Island Jewish Health System)
Determination/Notification for IRB of Record for Human Subject Research Projects
Determination/Notification for IRB of Record for Human Subject Research Projects (GU Stock Form)
Other Forms
MRI-GU Protocol Review Form for Reviewers Amendment and Continuing Review Form for Reviewers Study Specific Disclosure Form � � OHRP Investigator 101 Training Completion Form

Get the new Adobe Reader

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