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Sponsored Programs Administration
Sponsored Programs Administration
Institutional Review Board (IRB)
...for the protection of human participants in research
Contacts | FAQ's | Forms | Guidelines | Meeting Schedule | Resources | Training
Resources
Example Consent, Permission and Assent Documents:
- Exempt Status Survey conducted by Graduate Student
- Exempt Status Interview, bulleted format
- Oral script for phone interview
- Expedited Interview, Hard copy consent, with signatures
- Parental Permission form where child is <7 yrs of age
- Parental Permission form (to be used with assent form)
- Youth Assent form (13-17 yrs of age)
- Child Assent form (7-12 yrs of age)
PowerPoint Presentation from School of Education Presentation (Oct. 16, 2009)
Regulations, policies and guidance:
- NDSU Policy: Research on Human Subjects
- The Belmont Report
- U.S. Office of Human Research Protections (OHRP)
- U.S. Food and Drug Administration
- OHRP FAQs: Investigator Responsibilities, Research with Children, Informed Consent, and more
- OHRP Common Noncompliance Findings
- Protecting sensitive data and information in research (NIH)
- International Research - laws, regulations and guidelines (OHRP)
- ICMJE clinical trials pre-registration requirement FAQ
- Clinical Trial Pre-registration requirement ClinicalTrials.gov
- Data sharing policy for genome-wide association studies funded by NIH
- CDC Guidance on Definition of Research
Other related organizations:
- AAHRPP: Voluntary accreditation for human research protection programs
- ORI Office of Research Integrity (DHHS)
- Journal of Empirical Research on Human Research Ethics (JERHRE)
- The Hastings Center
Federal sponsors' human research protections policies:
- National Institutes of Health
- Dept. of Navy
- National Science Foundation
- Center for Disease Control
- Environmental Protection Agency
- Office of Naval Research
- National Institutes of Justice
- Dept. of Education
- Dept. of Energy
Recent news, information or announcements:
- Protecting Research Participants a Priority: Rep. DeGette introduces legislation to strengthen human research protections
- The Hastings Center article: 'Reformed Consent'
- OHRP Request for Comments on Institutional Review Boards
- FDA 101: Clinical Trials and Institutional Review Boards
- NIH announcement 'Protecting Aggregate Genomic Data'
- OHRP Request for Comment: Human Subjects Protection Training and Education Programs
Last updated: October 14, 2009 2:26 PM
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