| FORMS AND SUBMISSION REQUIREMENTS | |
| Initial Submission | |
Protocol Form (Revised 8/09) The Biosafety Coordinator must complete the risk assessment section of the form prior to submission. Use for Recombinant DNA, Infectious Agents or protocols which have toxins |
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| Continuing Review | |
| Continuing Review Form - This form is generated by the IBC staff and forwarded to the investigator 2 months prior to study expiration. However, we have provided this electronic word version for your use. Please be sure to enter the approval dates from our notice into this form. | |
| Standard Operating Procedure Templates | |
| Template for Infectious Agents | |
| Amendments | |
| Amendment Form | |
| Unanticipated Events | |
Adverse Event Form -Use this form to report to the IBC any adverse event (E.g. accidental exposure, spills that may be environmentally dangerous, events requiring any type of medical attention) or any noncompliance with NIH guidelines. |
Instructions |
Last modified October 13 2009 10:06 AM
