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IRB: Institutional Review Board

• Applications
  • Application for Human Subjects Research Approval (Word)
  • Renewal Form (Word)
  • Modification Form (Word)
• Application Guidelines
  • IRB Application Guidelines
  • IRB FAQ
  • Decision Tree (PDF)
• Informed Consent
  • Consent FAQ
  • Consent Form Guidelines (PDF)
  • Assent Example (Word)
  • Survey Landing Page Example (PDF)
• IRB Committee
  
  • Current Board Members
  • IRB Bylaws (PDF)
• Safety and Monitoring
  • Adverse Event Reporting Form (Word)
  • Safety when working Off-Campus
• Conflict of Interest
  • Conflict of Interest Policy
  • Conflict of Interest Form
  • (MSU website)

IBC: Institutional Biosafety Committee

• Application for Biohazardous Materials Research Approval: Request from the ORC
• (MSU website)

Other Resources

. To fully understand the laws and ethics related to human research, training is available.

Responsible Conduct of Research (RCR): Required for most NSF and many NIH grants.

  (OHRP) provides US Department of Health and Human Services links to various compliance, social topics, and special issues of interest to researchers conducting any type of research involving human subjects.

(ORI)
The ORI develops policies, related to the detection, investigation, and prevention of research misconduct and the responsible conduct of research.

(IACUC) provides forms, guidelines, and training for animal researchers.

(e-CFR)
Human subjects research and Institutional Review Board regulations are federally governed by:

• Health and Human Services Code of Federal Regulations Title 45:
• Food and Drug Administration Code of Federal Regulations Title 21:

Return to the main IRB page