You are on a committee that wants to perform a study on diabetic patients. The IRB has given the committee permission to perform the study on human subjects. Prior to the study, you will need to get consent from the subjects that will be a part of the study.

In preparation for requesting consent from the study participants, complete the following:

1. Create a consent form that outlines the information required by federal regulations.
2. Fill out your consent form using fictitious information.
3. Be sure that your form is free of spelling and grammar errors.