Protecting Human Participants
The Institutional Review Board (IRB) reviews projects that involve human participants to uphold two broad standards: first, that participants are not placed at undue risk; and second, that they give uncoerced, informed consent to their participation.
With participation from a wide range of health department programs and divisions, along with collaborations with outside agencies, the IRB provides review and oversight to numerous projects conducted by the North Dakota Department of Health.
For questions or more information contact IRB administrator, Tracy K. Miller, PhD, MPH at email@example.com
Step One: fill out the preview questionnaire and submit it to the IRB administrator. Upon review, the IRB administrator will let you know if you need to submit the IRB submission packet.
Download IRB applications, appendices, and other documents for submission request.
Find out what researchers need to know about IRB policy, best practices and frequently asked questions.
Find information on IRB training for investigators and research personnel.