This section contains all of the forms and consent templates that apply to investigators from:
• Business
• Education
• Engineering
• Humanities & Sciences
• Law
*Please note that when creating a protocol for IRB submission, these investigators need to select the Non-Medical eProtocol Application category.
* Any study that involves the collection and analyses of human biological specimens and/or Protected Health Information (PHI) will need to be submitted on the Medical eProtocol application.
For questions, please contact the Non-Medical IRB Panel Staff. If you are having trouble accessing these forms, please ask IRB Education (email or call 650-724-7141) to have them sent to you.
The consent/assent form should be in a language that is understandable to someone without a scientific background. Please use the Microsoft Readability Statistics tool as needed when writing your consent form.