If you are submitting a grant to the National Institutes of Health (NIH) or the National Science Foundation (NSF), you may receive a notification that your study is likely to be funded and that more ...

A student can conduct human subjects research under the supervision of an experienced faculty advisor. The faculty advisor must be identified on the student PIs initial submission as the principal ...

SODM research projects involving human subjects are required to obtain IRB approval from a "home" institution (CWRU or UH) before the start of any research activities. Use the information below to ...

Most Santa Clara University employees and students who plan to conduct research with human participants must obtain approval from the Santa Clara University Institutional Review Board (IRB) before ...

For your convenience, below is information about the IRB. Forms and processes for IRB submission are online. An overview on regulatory binder preparation and maintenance can be found in a presentation ...

The basis for the single IRB model is to allow multiple sites that are conducting the same protocol to use a single IRB for review, instead of using multiple IRBs to review the research at the sites ...

Research with human participants in countries outside the United States must comply ethical standards. Additional considerations may be required depending on the country of research. Furthermore, ...

All human subjects research connected with members of the Smith College community (either as researchers or study participants) must be reviewed and approved by the IRB prior to the initiation of the ...

California Lutheran University's Institutional Review Board's (IRB) primary responsibility is to protect the rights, welfare, and privacy of all human participants in research conducted by California ...

Single IRB Review is an arrangement in which one institution's IRB provides review, approval and oversight for the Human Research activities of multiple institutions. This is intended to streamline ...