Institutional Review Board

The Samuel Merritt University Institutional Review Board (IRB) reviews research projects to ensure that two broad standards are upheld: first, that subjects are not placed at undue risk; and second, that they give uncoerced, informed consent to their participation. With representation from a wide range of scientific disciplines and from outside the academic community, the IRB gives timely but individualized attention to the numerous research projects at the University.

More Information

Investigators conducting research are responsible for reporting any unanticipated problems or adverse events involving risks to research participants. Please submit a written report of any such problems by filling out the Adverse Event Report Form and submitting it to the IRB Administrator immediately.

If your study is now complete, please fill out the Final Report Form and submit it to the IRB Administrator.

Research Requires IRB Review If

• It uses humans, human tissue, or data gathered on human subjects; and

• It is performed by University faculty, students, or staff; on University premises; with University equipment; or on University faculty, students, or staff.

• It is performed by University faculty, students, or staff at Alta Bates Summit Medical Center. Note: You must also get IRB approval from Alta Bates Summit Medical Center, and submit proof of Alta Bates Summit IRB approval to the Samuel Merritt University IRB.

IRB Submission Deadlines

Full committee review:  The deadline is the first working day of the month.  The IRB meets monthly, as needed, except for the months of August and December.

Expedited review:  Proposals can be submitted at any time.

Exempt review:  Proposals can be submitted at any time.

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