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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
- NDSU Policy: Research on Human Subjects
- 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
- AAHRPP: Voluntary accreditation for human research protection programs
- ORI Office of Research Integrity (DHHS)
- 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
- Subject protections requirements of various federal funding agencies:
- 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
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