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Compliance

  • Institutional Review Board
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    • Guidelines & Policies
    • HIPAA
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IRB Guidelines and Policies

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General Guidelines  |  HIPAA Guidelines  |  NIH Requirements  |  How to Submit  |  IRB Charges  |  Meeting Dates


General Guidelines

  • Guidelines for Research Involving Human Subjects (PDF format)
  • Glossary of Simplified Terms (PDF format)
  • Legally Authorized Representative (PDF format)

To view "PDF" files, you will need to download a free copy of Acrobat Adobe Acrobat Reader.

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HIPAA Guidelines

  • Researcher's Guide to HIPPA FAQ

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NIH Requirements

  • NIH

  • IRB letter to PI

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How to Submit

  • 7 Types of submissions

  • How Long?

  • IRB Requirements (MS Word format)

  • Sutter Health IRB (SHIRB)

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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.

    • Meeting Schedules 2009
    • Meeting Schedules 2010

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