IRB Authorization Agreements
An IRB Authorization Agreement (IAA) is a special agreement between two institutions who are engaged in human subjects research. An IAA allows an institution with a Federalwide Assurance (FWA) to extend the applicability of its FWA to cover another institution. In practice, this means on institution's IRB will be the IRB of Record which reviews the study. These agreements help to minimize regulatory burden on the IRB review and approval process by limiting the IRB review to one institution. IAAs are sometimes referred to as IRB of Records. When signing the IAA, one institution is designated the lead IRB or IRB of Record.
IAAs can be requested by entering information within your Cayuse IRB submission.
1. The PI or primary contact should contact the MSU IRB for a preliminary conversation on using an IAA.
2. Once both institutions verbally agree to enter into the agreement, complete the appropriate IAA information required for IAAs within your Cayuse submission.
2a. If MSU is to be the IRB of Record (lead IRB), a study protocol or pending submission (in Cayuse IRB) must be available. or
2b. If MSU is to rely on another institution's IRB, please submit the other institution’s IRB approval, FWA #, and any other study related documents, such as consents within Cayuse IRB submission.
3. After signatures from both institutions have been obtained, the Research Compliance Officer will provide you with a final signed copy of the agreement.
It varies by institution. IAAs generally take a couple of weeks for processing, but the timeframe is ultimately driven by the availability of the Institutional Officials who are responsible for signing these agreements.
If you are working with a collaborator who is engaged in human subjects research, they must have IRB review and approval*. This can be accomplished one of two ways:
- The research team submits to both institutions for IRB approval; OR
- The research team requests an IRB Authorization Agreement (IAA).
*Note: Anyone covered by the IAA may not begin any work on the project until IRB approval has been granted AND the agreement has been signed by all parties.
MSU should be the IRB of Record if a MSU investigator is the prime awardee of a grant or other funding, or if the majority of research activities will take place at MSU with other institutions collaborating. If you are requesting MSU be the IRB of Record please provide the necessary information within the Cayuse IRB submission.
Another institution may be best served as IRB of Record if all research activities are taking place there, or if the MSU IRB does not have the relevant expertise to review a study (i.e. clinical trial at external medical facility).
Usually the Research Compliance Officer, the IRB Chair and Staff in consultation with the researchers will decide if an IAA is appropriate. The funding source, potential risks of harm to research subjects and the research site where the risks are incurred are factors in making the decision. Students conducting their thesis or independent study at a collaborating site must still submit to the MSU IRB for approval.
If you are not interacting with human subjects or collecting or analyzing identifiable information, your role on the project does not meet the definition of research with human subjects. You do not need IRB approval.
IAAs last for the duration of the research study or for however long the collaborator remains engaged in human subjects research. They need not be updated unless an expiration date is provided or the Principal Investigator (PI) or study information changes.
After obtaining an IAA you will need to do the following:
If MSU is the IRB of Record, you should continue to correspond with the MSU IRB as you would normally do, such as submitting renewals, modifications, or closure requests.
If the other institution has been designated the IRB of Record, you should correspond with the other institution and submit renewals, modifications, and closure requests in accordance with their local procedures. You must contact the MSU IRB if any of the following are true:
Change in risk level for the study;
Unanticipated problem involving risk to subjects or others;
Suspension or termination of the research by the investigator, IRB, or sponsor;
Change in PI;
Change in funding arrangements;
Change in MSU staff roles and responsibilities; OR
Closure of the study.
No. However, data sharing should be done in a manner consistent with your MSU IRB approved study and any agreements made with research subjects about the use of their data.