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Electronic Submission Database (eIRB)

The NASA IRB uses an electronic submission system for the review of human research studies called eIRB. The site contains information that is accessible to the public, such as meeting dates and standard operating procedures. One must have a registered account in order to submit or alter studies.

Visit the eIRB about Electronic Submission Database (eIRB)
Astronaut Mark T. Vande Hei, Expedition 53 Flight Engineer (FE), exercises on the Combined Operational Load Bearing External Resistance Treadmill (COLBERT) T2 in the Node 3.

Follow the Submission through the eIRB

The eIRB system uses “states” to classify where a submission is in the review process. The diagram below demonstrates the workflow a submission will undergo, from the “Pre-Submission” state to “Review Complete”.

The following table defines some possible study states a submission could be in during the course of its review.

Pre-SubmissionThe application is under preparation by the Principal Investigator (PI) or submission preparer.
Clarification RequestedThe IRB Coordinator has requested changes or clarification. The PI and Primary Contact will receive an e-mail notification advising them of the request.
Pre-Review CompletedThe submission awaits assignment to a Designated IRB member for review.
Non-Committee ReviewThe submission is currently being reviewed by an IRB member.
Committee ReviewThe submission awaits assignment to the Convened IRB for review or the submission has been assigned to an IRB meeting and is being reviewed by the IRB members.
Post ReviewThe IRB letter advising the PI of the Board’s or IRB member’s decision is being prepared.
Review CompleteReview of the submission is complete and a letter has been sent.

Submission Methods

Below are several categories of submissions that are used in the eIRB. Click on the categories to become familiar with them and read the attached document to learn how to submit them in the eIRB.

New Study

Before submitting a new study, determine the Principal Investigator and identify the study team. All members of the study will have completed human subjects protections training and conflict of interest requirements. Develop the study protocol, informed consent, and gather supporting documents such as advertisements and questionnaires/surveys. Review all documents thoroughly for consistency before submission.

Learn how to submit a new study

Contact the NASA IRB / Return to the NASA IRB Homepage