Biomedical IRB-01
- Application for IRB Review (to be used for expedited and convened meeting initial reviews)
- Attachment A: Expedited Review Categories
- Attachment B: Research Involving Children
- Attachment C: Research Involving Pregnant Women or Fetuses
- Attachment D: Research Involving Prisoners
- Attachment E: Research Involving Adults with Diminished Decision-Making Capability
- Attachment F: Research Involving Investigational New Devices
- Attachment G: Request for Waiver of Consent/Permission/Assent or Documentation of Consent/Permission/Assent
- Reporting Form for Scientific/Methodological Review
- Application for Continuing Review/Project Termination
- Application for Modification of Approved Research
- Application for Request for Review of Supplemental Documents
- Application for Response to IRB Requests
- Reporting Form for Reportable New Information (formerly Reporting Form for Unanticipated Problems Posing Risks to Subjects and Others (Including Reportable Adverse Events))
Social Behavioral IRB-02
- Application for IRB Review (to be used for expedited and convened meeting initial reviews)
- Attachment A: Expedited Review Categories
- Attachment B: Research Involving Children
- Attachment C: Research Involving Pregnant Women or Fetuses
- Attachment D: Research Involving Prisoners
- Attachment E: Research Involving Adults with Diminished Decision-Making Capability
- Attachment G: Request for Waiver of Consent/Permission/Assent or Documentation of Consent/Permission/Assent
- Reporting Form for Scientific/Methodological Review
- Application for Continuing Review/Project Termination
- Application for Modification of Approved Research
- Application for Request for Review of Supplemental Documents
- Application for Response to IRB Requests
- Reporting Form for Reportable New Information (formerly Reporting Form for Unanticipated Problems Posing Risks to Subjects and Others (Including Reportable Adverse Events))
Exempt Research
- Application for Determination of Exempt Status
- Application for Determination of Exempt Status: Educational Research
- Application for Determination of Exempt Status: Observation, Study, Interview
- Application for Determination of Exempt Status and HIPAA Authorization Waiver for Medical Record Review
- Application for Determination of Exempt Status: Use of Biological Specimens in Research
- Application for Continuing Review/Project Termination
- Reporting Form for Reportable New Information (formerly Reporting Form for Unanticipated Problems Posing Risks to Subjects and Others (Including Reportable Adverse Events))
- Application for HIPAA Waiver
External Review
Web Page Recruitment Application
Confidential Research Hotline (402-280-3200)
Research Personnel are expected to report any known or suspected noncompliant conduct related to research or sponsored program activities conducted and/or approved through Creighton University. The confidential Research Compliance Hotline (402-280-3200) is available for any individual who wishes to remain anonymous and/or has found other available reporting mechanisms to be ineffective. Research Personnel may also address their research compliance-related questions or concerns to Kathy Taggart, Associate Vice President for Research and Compliance, at 402-280-2360.
