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Office of Regulatory Affairs

INSTITUTIONAL REVIEW BOARD (IRB)

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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?
NEW! 03/07/2008

IRB Forms and Cover Letters

MRI-GU Application for Oncology IRB Review.
(D-1)
Please use for expedited applications only
NEW! 01/02/2008
MRI-GU Continuing Review Form
(D-2) NEW! 01/02/2008
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 NEW! 11/29/2007
Network Form
(D-6)

Informed Consent From Templates and Guidelines

Joint MRI-GU Informed Consent Template NEW 08/28/2007!
Required elements of a consent form
NEW 01/23/2007!
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
NEW 02/13/08!
Guidelines for Completing an Informed Consent Form
Glossaries of Lay Terms
NEW 01/16/2007!
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)
NEW 10/20/06!

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


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