Nonmedical Research
Forms

The eProtocol System is used for:

• New Protocol applications -see Sample Nonmedical Application Questions.
  Investigators will need to identify the appropriate review type, which determines what questions must be answered on the protocol application.
  
• Modifications to approved protocols; need prior IRB approval to implement.
• Continuing Review applications.
• Reports - unanticipated problems, events/information requiring prompt reporting.
• Final Reports - to close a protocol; not required for Exempt research.

Click here for eProtocol.    
Questions about eProtocol? See eProtocol Help.

Contact the IRB 2 Manager (650-723-2480) with any questions about submissions for nonmedical research.

Forms and Templates

• Nonmedical Consents - Consent Form Templates and Consent Process Information
  
  
• Determination of Human Subject Research application
  Federal regulations require IRB review of all human subject research. Some categories of research are difficult to discern as to whether they qualify as human subject research. The IRB has established policies and procedures to assist in this determination. Complete this form and return it to the IRB Coordinator if you want the IRB to determine whether your activity constitutes human subject research. For help, contact the Research Compliance Office.
  

• Scientific Review:
  • Review of Scientific and Scholarly Validity, and Oversight (by Faculty Sponsor)
  • Review of Scientific and Scholarly Validity (Dept Chair or School Dean)
    
    
• Letter of Agreement
  Use for STANFORD sponsored research in cooperation with other organizations or agencies.