CPMC Institutional Review Board (IRB)
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Policies and Procedures | Standard Operating Procedures | HIPAA Guidelines | National Institutes of Health (NIH) | How to Submit | IRB Charges | Meeting DatesPolicies and Procedures
- IRB Policies and Procedures (PDF format)
- Important Information about your IRB approval
- Experimental Subject's Bill Of Rights in many languages
- Glossary of Simplified Terms
- Legally Authorized Representative (Being updated)
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Standard Operating Procedures
- Study Modifications
- Initial IRB Review of Proposed Research (PDF format)
- Expedited IRB Review
- Continuing Review of IRB-Approved Research
- Investigator Reporting and IRB Review of Protocol Violations and Deviations (PDF format)
- Protocol Violation/Deviation/Exemption Summary Report
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HIPAA Guidelines
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National Institutes of Health (NIH)
See: National Institutes of Health (NIH) at www.nih.gov
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How to Submit
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IRB Charges
IRB fees apply only to those studies that are funded by a private company such as a pharmaceutical or device company. For all other studies, list as “PI Self-funded” on the research application (and there will be no charge).
There is no fee for items that are coming back to the IRB or an expedited reviewer for a follow-up review (e.g., clarification requests) that have already been billed for the initial review, modification or continuing review.
Fee Schedule
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Meeting Dates
Panel 1 meets on the 2nd TUESDAY of each month at noon in the Anne R. Thorton Boardroom, 2351 Clay Street, 3rd Floor, Stanford Building.
Panel 2 meets on the 4th TUESDAY of each month at noon in the Anne R. Thorton Boardroom, 2351 Clay Street, 3rd Floor, Stanford Building.
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