|
|
== Informed Consent & Review Form
Project Director:
Date:
Project Title:
Some research involving human subjects requires that the subjects complete INFORMED CONSENT forms. Do not assume that your research requires such a form. The IRB Chairman/Committee will determine if an informed consent form is required after review of your research protocol. If a form is required, you must submit a proposed form for approval. See the reverse for general guidelines and principles regarding Informed Consent. Attach your proposed form or complete in the space below.
]
]
]
]
]
]
]
]
]
]
]
]
]
]
]
FOR IRB USE:
INFORMED CONSENT FORM APPROVED
INFORMED CONSENT IS NOT APPROVED, SEE ATTACHED SUGGESTED REVISIONS
INFORMED CONSENT IS RECOMMENDED FOR FULL BOARD REVIEW
Signature of IRB Reviewer:
Date:
{http://www.nih.gov/grants/oprr/humansubjects/guidance/ictips.htm 45 CFR 46.116 General requirements for informed consent.}
]
]
 |
 |