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 WMREF Investigator's Summary Form.doc
WMREF IRB Investigator's Summary Form
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 National Studies.doc
Use this form for instructions on submitting a multi-site sponsored clinical trial to the WMREF IRB for approval.
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 Consent Checklist.doc
Use this checklist to help develop the consent form for any study, except for a pediatric study.
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 WMREF IRB Waiver of Consent Form Request.doc
If an investigator intends to request a waiver of consent for his/her research they must submit a WMREF IRB Waiver of Consent Form Request.
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 WMREF IRB Waiver of Consent Form Request.doc
WMREF IRB Waiver of Documentation of Consent Request
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 WMREF Checklist for Authorization to Use and Disclose PHI for Research Purposes Rev 040403.doc
Checklist for use and disclose of protected health information for research purposes.
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 WMREF Checklist for IRB Review of Pediatric Research.doc
WMREF IRB Checklist for IRB Review of Pediatric Research
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 WMREF IRB Checklist for Research Involving Pregnant Women or Fetuses.doc
WMREF IRB Checklist for Research Involving Pregnant Women or Fetuses
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 WMREF IRB Interim or Final Report Fillable Form.docx
Use this fill-able form for all study Interim or Final Reports. Electronic form is all that is necessary to send to the IRB. No hard copy necessary.
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 WMREF IRB Unanticipated Problem&Adverse Event Form.doc
This form should be used when reporting an unanticipated problem with a research protocol or adverse event occurs.
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