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 an Application to the IRB | IRB Charges | Meeting DatesPolicies and Procedures
- Important Information about your IRB approval
- Experimental Subject's Bill Of Rights in many languages
- Glossary of Simplified Terms
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Standard Operating Procedures
How to find the IRB Standard Operating Procedures in IRBNet:
Please login to www.irbnet.org.Opens new window with your username and password. Click “Forms and Templates” on your left hand menu for a listing of, and access to, the latest version of all available Standard Operating Procedures.
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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 an Application to the IRB
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IRB Charges
IRB fees are currently charged only to those studies that are funded by a private company such as a pharmaceutical or device company.
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. Thornton Boardroom, 2351 Clay Street, 3rd Floor, Stanford Building, PACIFIC CAMPUS, San Francisco, CA 94115.
Panel 2 meets on the 4th TUESDAY of each month at noon in the Anne R. Thornton Boardroom, 2351 Clay Street, 3rd Floor, Stanford Building, PACIFIC CAMPUS, San Francisco, CA 94115.
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