IRB Policy and Procedures
Policy and guidance governing human subject research, the protection of participants and the organization and conduct of the IRB is developed and maintained by IRB administration under the guidance of federal requirements (,Ìý, andÌý).
Policies are updated on a regular basis to ensure compliance with current requirements. Please make sure you are using the latest versions, which are available in theÌýSWAGÊÓƵInstitutional Policy and Procedure Handbook.Ìý Below is a list of the IRB policies and procedures.Ìý The research-related policies are grouped together and are searchable via the interactive table of contents.
Policy Number | Policy Description |
---|---|
R004 |
SWAGÊÓƵInstitutional Review Board Policies and Procedures |
R004A1 |
Institutional Review Board Self-Assessment |
R004A2 |
Emergency Use of a Test Article |
R004A3 |
IRB Member Conflict of Interest |
R004A4 |
IRB Administrative Fees for Protocol Review |
R004A5 |
SWAGÊÓƵPolicy on Compliance Auditing |
R004A6 |
IRB Guidance on Research Limited to Retrospective Medical Records Review |
R004A7 |
Procedure on Conducting and Documenting Continuing Review |
Ìý |
Procedure on Central Institutional Review Board (CIRB) Facilitated Review |
Ìý |
Procedure on IRB Review of Applications for HHS Support |
Ìý |
Procedure for Obtaining Informed Consent |
Ìý |
Procedure on Reporting of Compliance Audit Review Standard Operating Procedure |
Ìý |
Procedure on Review of Investigational Device Protocols |
R016 | SWAGÊÓƵPolicy on Case Reports and Case Series |