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    The Qatar University Institutional Review Board (QU-IRB)

    Institutional Review Board (QU-IRB)

    QU-IRB oversees research involving human participants to protect their rights, safety, and well-being. We ensure all proposals comply with ethical principles, national regulations (MOPH), and international standards.

    Core Responsibilities

    Review & ApprovalEvaluation of all research projects involving human subjects.
    Risk MitigationProviding guidance on informed consent and participant confidentiality.
    ComplianceMonitoring adherence to Ministry of Public Health (MOPH) directives.

    Application & Submission

    Researchers must submit applications exclusively through the IRBNet platform. Email or physical submissions are not accepted.

    Access IRBNet Portal

    Required Application Package

    Application Form: Use the IRBNet wizard for English; use the downloadable Word form for Arabic research.
    Data Collection Tools: Questionnaires and interview guides must be provided in every language used. Multi-Language
    Informed Consent / Assent: Required for all participants. Assent forms are mandatory for children ages 7–17.
    External Approvals: Include approval letters if the research is conducted at another institution.

    Training Requirements

    For English Research (CITI):
    • Social-Behavioral-Educational (SBE) Course
    • Biomedical (Biomed) Comprehensive Course
    • Biomedical Data or Specimens Only Course
    For Arabic Research:

    Watch the "Ethics in SBE Research" video and contact qu-irb@qu.edu.qa to schedule your exam and obtain a certificate.

    Frequently Asked Questions

    What types of research require IRB review?
    Any research involving human subjects must undergo IRB review to ensure ethical acceptability. 
    Do I need QU-IRB approval if I have approval from another institution?
    Yes. If you are affiliated with Qatar University or the research is conducted here, you must obtain QU-IRB approval regardless of prior approvals. 
    Can I start research before receiving IRB approval?
    No. Research involving human subjects must not commence until official IRB approval is granted. Failure to comply is a serious ethical violation. 
    How long does the review process take?
    Duration varies based on the risk level and complexity of the study. We strive to provide feedback as timely as possible. 
    Can I make amendments after approval?
    Yes. Any changes to the protocol must be submitted for review and approval before they are implemented.