Skip Navigation Genome.gov - National Human Genome Research InstituteGenome.gov - National Human Genome Research InstituteGenome.gov - National Human Genome Research InstituteNational Institutes of Health
   
       Home | About NHGRI | Newsroom | Staff
Research Grants Health Policy & Ethics Educational Resources Careers & Training

Home>Research>Intramural Research>Clinical Research >NHGRI Institutional Review Board (IRB)
Print Version

NHGRI Institutional Review Board

Overview

The National Human Genome Research Institute (NHGRI) Institutional Review Board (IRB) is responsible for protecting the rights and welfare of the human subjects of research conducted by intramural investigators at NHGRI.

All intramural research protocols involving human subjects must be submitted for review by the NHGRI IRB. These Web pages contain the instructions, forms and relevant links for submitting a research protocol to the IRB.


IRB News and Updates

NOTE: Effective immediately, investigators must complete and submit a Designation of Reimbursement for Travel and Subsistence (DRTS) Form (NIH-2868) PDF icon along with initial and continuing review applications to the IRB. This is in response to a new NIH policy (M08-1) PDF icon regarding reimbursement of travel and subsistence expenses for participants in intramural research protocols.

Please note that the "Points to Consider" area located at the top of the DRTS form must be filled out even when reimbursement is not being provided. Also, all new and actively recruiting protocol consent documents must include the following statement: "Reimbursement for travel and subsistence will be offered consistent with NIH guidelines."

January 30, 2009

Investigators submitting new on-site protocols for initial IRB review are required to complete and submit a Clinical Center Resource Assessment Tool form Microsoft Word. This form should be submitted to the NHGRI IRB office as soon as possible after the completion of the scientific review, no later than the due date for the submission of the entire IRB packet for review. A Protocol Resource Pilot flow chart PDF icon is available that further describes this review process.


Top of page

Contacts

Victoria Willits
IRB Coordinator
10 Center Drive, CRC
Building 10 CRC, Room 6-3340
Bethesda, MD 20892-1611
Phone: (301) 496-1906
Fax: (301) 480-3015
E-mail: vwillits@mail.nih.gov

Sara Hull, Ph.D.
Director, NHGRI Bioethics Core
IRB Vice-Chair and Administrator
Phone: (301) 435-8712
E-mail: shull@mail.nih.gov

Ben Berkman, J.D., M.P.H.
Deputy Director, NHGRI Bioethics Core
Phone: (301) 496-1531
E-mail: berkmanbe@mail.nih.gov

Fabio Candotti, M.D.
IRB Chair
Phone: (301) 435-2944
E-mail: fabio@mail.nih.gov


To view the files on this page, you will need Adobe Acrobat Reader.Download Adobe Acrobat Reader

To view the Microsoft Word files on this page, you will need MS Word. A copy of the latest version of Word Viewer can be downloaded for free.


Top of page

Last Updated: April 23, 2009



PrivacyCopyrightContactAccessibilitySite MapStaff DirectoryFOIAHome Department of Health and Human Services  National Institutes of Health  USA.gov