Application Materials
If you have any questions about application materials or the process, please contact the IRB at 229-312-0372.
- Adverse Events / Unanticipated Problem Form
- Amendment / Modification Request Form
- Application for Humanitarian Use Device
- Emergency Use Procedure Consent Form and HIPAA Authorization (Template)
- Emergency Use Report Form
- Enrollment Closure Form
- Application for Final Study Closure
- IRB Informed Consent Checklist
- Initial Review Form
- Continuing Review Request 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 and Unanticipated Risk Reporting
- Allegations of Non-Compliance, Concerns or Complaints
- Closure of Studies
- Compassionate Use: Investigational Devices Policy
- 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
- Initial Review and Primary Reviewer System
- Institutional Review Board (IRB) Informed Consent
- Institutional Review Board (IRB) Jurisdiction and Authority
- Institutional Review Board (IRB) Membership
- Institutional Review Board (IRB) Payment to Subjects
- Institutional Review Board (IRB) Record Keeping
- Institutional Review Board (IRB) Use of Non-Local IRBs
- Institutional Review Board (IRB) Voting
- Non-English Speaking Subjects and/or Legally Authorized Representatives
- Planned Emergency Research
- Principal Investigator Recordkeeping Responsibilities
- Research Revisions and Amendments
- Subject Recruitment and Review of Advertisements
- Vulnerable Populations Research
Phoebe does not currently conduct or support studies involving prisoners, pregnant women, human fetuses or neonates.