Institutional Review Board (IRB)

What is an IRB?

An Institutional Review Board (IRB) is a committee that performs ethical review of proposed research to help assure the protection of the rights and welfare of human participants. The IRB approves the initiation of and conducts periodic reviews of research involving human participants. Investigators also share the responsibility for protecting human participants.

To submit a new application, please visit Kuali-IRB. For more information on how to submit via Kuali-IRB, please click here.

To submit an amendment, continuing review, reportable event, or closure for a project already approved in IRBNet, visit IRBNet and use the guidance on the IRB Process page. 

Review Paths

Human Subject Research Determination

If you are unsure if your project requires IRB review and approval, please complete and submit the HSRD Form through Kuali-IRB. You will receive an official determination confirming no IRB Approval is needed or additional information will be requested.

Exempt Review

To receive an Exempt Determination from the IRB, a protocol must fall into one or more of eight (8) federally-defined exempt categories. Examples of Exempt research are: anonymous surveys/interviews, passive observation of public behavior without collection of identifiable information, retrospective chart/record/data reviews, analysis of discarded pathological specimens without identifiers, etc.

Expedited Review

To qualify for an Expedited Review, research should fall into one or more of nine (9) federally-defined Expedited categories and present no greater than minimal risk to participants.

• Expedited Review Guidance and Categories 

Full IRB Review

Protocols which do not meet either Exempt or Expedited review criteria will be added to the next available agenda for review at the fully convened IRB Meeting. Research activities presenting greater than minimal risk or transactions increasing the potential risk, will always be referred to the full convened IRB Meeting for review.

Submission Deadlines and Meeting Dates are available on this page by clicking Full Board Meeting Dates and Deadlines at the top.

IRB Composition

The IRB is a review committee consisting of faculty, students, staff, and outside members that has been established to help protect the rights and welfare of human participants participating in research. It is established to evaluate the ethical implications and conduct a risk-benefit analysis of research involving human participants through the application of 45CFR46 (Code of Federal Regulations governing human subject research).

For additional information regarding the review committee, the Office for Human Research Protections' (OHRP) provides the webinars listed below:

• IRB Review Criteria
• Quorum and Voting in IRB Meetings
• Membership Requirements for Institutional Review Boards (IRB)

Federalwide Assurance

FWA: 00005856
IRB Registration: IRB00000474
IRB Organization: 0000281

To check the expiration dates for these Assurances, please refer to the Department of Health and Human Services website for the Office for Human Research Protections (OHRP) database.

The University of Maryland College Park Federal Wide Assurance and the IRB registration are listed under "U of Maryland Coll Park Campus."

Kuali System Status

Use this link to check on the status of outages or issues for Kuali products. The UMD IRB platform is Kuali Build: https://status.kuali.co/

Standard Operating Procedures and Policies

This resource provides a detailed outline and thorough description of the Standard Operating Procedures that are specific to the UMD Office of IRB Operations:

UMD IRB Standard Operating Procedures

This is the overarching University Maryland System Policy on Human Subjects of Research:

IV-2.10- UNIVERSITY OF MARYLAND SYSTEM POLICY ON HUMAN SUBJECTS OF RESEARCH

Virtual Appointments with the IRB Office

 The IRB Office offers virtual appointments to provide general IRB guidance, answer questions regarding IRB processes, and offer technical assistance with the electronic submission system.

Each appointment will be limited to 15 minutes.

To register for a virtual IRB appointment, please complete this form in its entirety. You must complete this form using your UMD-affiliated email address.

Please Note: The IRB staff will not provide any IRB determinations. In order to receive an official IRB determination, please submit an IRB application through Kuali-IRB.

If your question requires immediate attention, please email irb@umd.edu.

Time to IRB Review

Most studies at UMCP meet the definition of minimal risk and thus receive exempt or expedited determinations - these studies are reviewed on a continuous basis and are generally NOT subject to the Full Board deadlines below.

Time to IRB review is the estimated time it takes from the date of completed submission to the time when modifications are requested by IRB staff. This is not the same as the time to approval.

Time to review may vary based upon timing in the semester and current volume of submissions. The busiest times of year at the IRB are: mid-Fall semester, prior to Thanksgiving break, prior to Winter Break, mid-Spring semester, and prior to Spring Break. Please also note that the IRB Office is closed when the University is closed.

You may experience delays in IRB review during the transition to Kuali-IRB (January - September 2026).

In general, completed submissions are reviewed in the order in which they are received. Investigators with urgent requests requiring immediate review should contact irb@umd.edu and briefly describe the specific circumstances. We will do our best to accommodate your request.

Avoiding Delays in Review

• Consult the IRB Process page and Transition to Kuali-IRB page for guidance.
• Respond to modifications promptly. The faster you are able to address modifications requested by the IRB staff, the faster the project will be moved forward to the final reviewer. In other words, projects with ongoing review are prioritized over new submissions.

Per Federal regulations and institutional policy the Full Board reviews protocols where one or more of the following are true of the research: (1)  it involves greater than minimal risk to human subjects, (2) it does not meet the criteria for one of the categories of expedited review, and/or (3) it has been referred to the committee by an IRB Member.

Regardless of risk level, a project may require full board review when the research involves:

• Vulnerable populations (including prisoners)
• Sensitive topics, including illegal activity
• Complex research design/methods requiring the expertise of multiple board members to evaluate