Beginning May 1,1999 any application approved for research using human subjects will require that the approved consent form include a label from the IRB giving the protocol number and the date approved. This will ensure that the correct, approved version is being used. It will also serve as a reminder of when the protocol must be reviewed again.

It will be necessary to submit the actual approved version in the format you intend to use. The IRB Coordinator will affix the label and return it to you through campus or US mail. If you prefer, you may pick it up from the Office of Research Support Services, Administration 315.