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Human Subjects Division (HSD)

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Document Details

Last Updated 11/22/2013
Version 4.60
Filesize 128.5 KB
Audiences Researcher
Doc Type Form

REQUEST AUTHORIZATION: UW/CC-IRB

Purpose

The Cancer Consortium IRB (CC-IRB) is not authorized to review University of Washington (UW) human subjects' research activity until this form has been completed and sent to the UW Human Subjects Division. The CC-IRB Clinical Research Support Office must first sign this Cover Sheet, which they will then forward to HSD.

Change Notes

  • Related to Ver. 4.60, noted 11/22/2013 @ 11:48am
    Added directionals to \"Access to Medical Records\" section. Please use this version going forward.
    - sherrye
  • Related to Ver. 4.50, noted 10/19/2013 @ 05:11pm
    Updated name to new naming convention on website.
    - sherrye
  • Related to Ver. 4.50, noted 09/27/2013 @ 02:57pm
    Name change from Protocol Office to Clinical Research Support
    - sherrye
  • Related to Ver. 4.40, noted 04/26/2013 @ 11:27am
    Updated name of Protocol Office to Clinical Research Support. Okay to use previous version.
    - sherrye
  • Related to Ver. 4.30, noted 03/29/2013 @ 08:32am
    Added question related to the IBC. Okay to use previous version.
    - sherrye
  • Related to Ver. 4.20, noted 01/14/2013 @ 10:47am
    Updated Conflict of Interest text.
    - sherrye
  • Related to Ver. 4.10, noted 01/03/2013 @ 03:28pm
    Updated contact information for Clinical Trials Administrator. Okay to use previous version.
    - sherrye