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| Institutional Approval Forms | |
| Institutional Approval Forms: | | All projects except those exempt from IRB approval need forms completed for institutional and IRB approval. | | Institutional approval form, D-I. Required of all projects needing expedited or full IRB review. | | Additional approval form, D-II. For research dealing with Pharmacy, Laboratory, Biohazards. | | IRB forms, D-III. With directions for structured description of research plans. (Required of all projects needing expedited or full IRB review.) | | Pregnant Women, Neonates, D-IV (PWS). | | Research study progress report form, D-IV.a. Must be sent to the IRB annually. | | Adverse event report cover sheet, D-IV.b. Must be sent to the IRB within 30 days of an adverse event. | | Amendment Cover sheet, D-IV.c. | | Wards of state and detainees, D-IV WS DS. | | Informed consent forms, D-V. templates for adults, children, and subjects without decision making capacity, along with advice on language to use for various types of studies.
| | HIPAA Authorization. | | Tips. On submitting requests for IRB exemption or IRB expedited and full review. | Research in the community or any outpatient clinic. Requires separate approval from the Ambulatory and Community Health Network Committee (Co-Chairs: Linda Rae Murray MD MPH and Mildred Williamson MSW; Woodlawn Health Center; 773-753-5500).
IMPORTANT: Input and approval should be sought well in advance of submitting any documents for IRB approval. Call the above phone number to obtain the necessary forms.
| | Old IRB web site. |
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