Application Materials

If you have any questions about application materials or the process, please contact the IRB at 229-312-0372.

• Adverse Event / Unanticipated Problem Report Form
• Amendment / Modification Form
• Application for Humanitarian Use Device
• Emergency Use Consent Form Template
• Emergency Use Report
• Enrollment Closure Form
• Final Study Closure Application
• Informed Consent Checklist
• IRB Application for Initial Review
• IRB Continuation Form
• IRB Determination Form
• IRB Fee Schedule
• Protocol Closure or Suspension Form
• Protocol Deviation Report Form
• Request for Exemption
• Request to Reopen a Closed Study

Supplemental Forms:

• Additional Research Personnel
• Financial Conflict of Interest Disclosure Form
• Multiple Adverse Events Reporting Form
• Research Involving Cognitively Impaired Individuals
• Research Involving Stored Data for Future Use
• Request for Approval of Deception in Research
• Request for Waiver of Consent
• Request for Waiver of Written Consent
• Use of Internet in Human Participants Research
• Waiver of HIPAA Authorization

Policies and Procedures:

• Adverse Event / Unanticipated Problems Reporting Policy
• Allegations of Non-Compliance, Concerns or Complaints
• Closure of Studies
• Continuing Review
• Emergency use of Drugs, Biologics, and Devices
• Exempt Review
• Expedited Review
• Expiration of IRB Approval and Subsequent Notice to Cease Study Activity
• Financial Conflict of Interest
• Human Subjects Research Policy
• Humanitarian Use Devices
• Informed Consent
• Initial Review and Primary Reviewer System
• Jurisdiction / Authority
• Membership
• Non-English Speaking Subjects
• Payment to Subjects
• Planned Emergency Research
• Record Keeping
• Research Revision
• Use of Non-Local IRBs
• Voting

Phoebe does not currently conduct or support studies involving prisoners, pregnant women, human fetuses or neonates.