The 涩里番下载 Institutional Review Board (IRB) is required by federal regulations to review all human subjects research activities conducted for which: (1) the conduct or recruitment of the research involves 涩里番下载 resources (property, facility or funding, including extramural funds administered by 涩里番下载); (2) the research is conducted by or under the direction of any employee, student or agent of 涩里番下载 in connection with his or her institutional responsibilities; (3) the research is conducted by or under the direction of any employee, student or agent of 涩里番下载 using any property or facility of 涩里番下载; or (4) the research involves the use of 涩里番下载鈥檚 non-public information to identify or contact human research subjects or prospective subjects.

涩里番下载 files a Federalwide Assurance (FWA) with the Department of Health and Human Services/Office of Human Research Protections (DHHS/OHRP).  涩里番下载鈥檚 FWA assures the government and the public that it will comply with federal regulations for the protection of human research subjects.

The function of the IRBs is to ensure adherence to all federal, state, local, and institutional regulations concerning the protection of the rights and welfare of human subjects participating in research. 涩里番下载鈥檚 IRB review is required for both funded and non-funded human subjects research.

The IRB鈥檚 role at 涩里番下载 extends to all research involving human subjects whether conducted by faculty, staff, or students. The purpose of the IRB is to inform and protect human subjects used in research. The IRB acts as an advocate for the research subject. This means that the IRB, during its review of a research project and the informed consent, has the right and responsibility to ensure that the research subject is fully informed of the procedures involved in the study as well as the risks.