IRB Application Packages
Forms and templates provided below.
Initial Review Application Package. Includes the following:
Protocol Amendment Package. Includes the following:
Continuing Review Package. Includes the following:
Closing Research Protocol. Includes the following:
IRB Forms and Documents
Initial Review Application
Request approval of research involving human subjects
Modify approved research
Continuing Review Form
Extend IRB approval
Standard Informed Consent
Signed informed consent form
Oral Consent Template
Waiver of Documented Consent
Waive requirement to obtain signature on consent form
Waiver or Alteration of Consent
Waive entire consent process or waive individual elements of informed consent
Scientific Review Form
Conflict of Interest Form
End of Experiment Form
Required at approval expiration to close research protocol
Unanticipated Problems & Serious Adverse Events
Report problems and adverse events with your research to the IRB
IRB Ethics Training
CITI Registration Instructions
Training is required for each member of the research team who will have access to data or will interact with subjects.
IRB Review Agreements & Assurance Coverage
Individual Investigator Agreement (IIA)
Used when co-investigator is not covered by a Federal Wide Assurance (FWA) with a DOD Addendum.
Institutional Agreement for IRB Review (IAIR)
Used to name one IRB the IRB of record when research is covered under multiple IRBs.
Please submit signed IRB Applications to Mrs. Rikki Nguyen in HA-206. All questions and comments concerning the IRB can be emailed to firstname.lastname@example.org or email@example.com.