IRB Forms
IRB PROTOCOL FORMS
|
Form |
Purpose |
| Request for Initial Review | This form is used to request a review of your proposed human subjects research by the IRB |
| Request for Addendum/Modification | This form is used to request the review and approval of changes to previously approved research |
| Request for Continuing Review | Your protocol will expire one year after the approval date. Use this form to renew or extend your approval. |
| Closeout Form | When you are finished with your study, with this form, you will notify the IRB office and your file will be closed |
| Unaffiliated Investigator Form | This form is used when investigators not affiliated with WCU are participating in a study |
| Additional Investigator Form | This form is used when more than five investigators will be involved with a research project |
The IRB Forms have been revised and updated!
The IRB will no longer review applications submitted on the old format, beginning March 1, 2013
PROTOCOL DEVIATION AND ADVERSE EVENTS
| Form | Purpose |
| Deviation or Violation Event Form | Click Here for guidance on the use of the Deviation or Violation Event Form |
| Adverse Event Form | Click Here for guidance on the use of the Adverse Event Form |
INFORMED CONSENT TEMPLATES
The Institutional Review Board has created several templates to serve as guides when creating your informed consent document.
The following forms are samples and templates that can be modified for your use:
- Sample of a completed consent form as an Outline
- Sample of a completed consent document in Paragraph form
- Sample of Template for SOTL
- Basic Template
- Descriptive Template
If your protocol will involve the recording of human subject, please utilize this additional informed consent guidance:
- Procedures for recording human subjects (voice or image)
- Addendum to Consent Form for recording human subjects
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