FOR ADDITIONAL INFORMATION/ FORMS |
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Please contact the Institutional Review Board or Office of Sponsored Programs if you have any questions regarding the IRB or the use and rights of human participants in research in general. |
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University of the District of Columbia Institutional Review Board
Angelyn Flowers, J.D., Ph.D., IRB Chair
Professor
Department of Urban Affairs, Social Sciences and Social Work
B41-315
(202) 274-5689
aflowers@udc.edu
University of the District of Columbia Office of Sponsored Programs
JoVita Wells, JD,
Director
Office of Sponsored Programs
Bldg 42, Rm 212G
202-274-6260
jowells@udc.edu |
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For further information, you are encouraged to visit the new OHRP human subject protections resource page at http://www.hhs.gov/ohrp/related.html This page provides links to reference documents, the Code of Federal Regulations 45 CFR 46, historical materials and Common Rule departments/agencies.
OHRP encourages all in the research community to use this reference page. |
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IRB Application and Consent Forms |
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| Continuing Review Application for Research Involving Human Participants |
| Application for Approval to Use Human Participants |
| Sample Informed Consent Form and Checklist |
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| Training for Researchers |
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| For the required training on protections for human subjects and other ethical issues |
| For training on the initial submission to the IRBNet.org |
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Prepared by the University of the District of Columbia Institutional Review Board (UDC IRB) with reference to the Institutional Review Board Guidebook (http://www.hhs.gov/ohrp/irb/irb_guidebook.htm). The UDC IRB acknowledges the assistance of the College of Charleston, which shared its web materials, on which UDC’s materials are based. The UDC IRB is also indebted to many other fine university web sites which it has visited in the course of preparing these materials, and in particular commends the design and content of the University of Maryland Baltimore Campus website. |
