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Institutional Review Board Human Subjects |
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IRB Info: Standard Application Application Instructions Consent: Helpful Links: IRB - Human Subjects (504) 280-7481 |
Welcome to the Office of We are located in Room 2076 in the Geology and Psychology building
WHAT IS RESEARCH? According to 45 CFR 46.102(d), research is defined as a systematic Any project fitting this description is subject to review and regulation by the Human subjects review is designed to protect both participants in research as well as the researcher by ensuring ethical reasearch design and practice. All research activities involving the use of human beings as research subjects (participants) must be reviewed and approved by the Institutional Review Board (IRB). Even though investigators are ultimately responsible for ensuring that the rights and the welfare of human subjects participating in research activities are protected, and that the methods used and information provided to gain subject consent are appropriate to the research, the IRB process assists investigators in this responsibility. For this purpose, investigators may not solicit subject participation or begin data collection until they have received written approval. IRB Application Review Process IRB approval is required before research can begin (including recruitment) and before proposals are submitted to any funding source. Studies which qualify for approval under expedited review or exempt status are thoroughly reviewed by the IRB Chair. Those protocols determined to require review by the full IRB will be scheduled for the next regularly scheduled IRB meeting. The primary investigator of a study may be required to attend such meetings. The full IRB generally meets the 15th of every month throughout the calender year. Click here for the full board schedule.
Proposals must be submitted by the submission deadline dates in order for |
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