Human
Phone:
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Forms, Templates, Checklists & Instructions
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The deadline for submissions to the HIC is noon on Tuesday, the week prior to the committee meeting. |
To view and print the following Adobe Acrobat PDF documents you will need Adobe Acrobat Reader. You may download a copy of this software, free of charge, from the ITS Web site.
Some forms are also available for downloading as Microsoft Word documents.
How Many Copies |
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MSWord Track Changes Instructions |
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FDA Certificate of Confidentiality Application Instructions |
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NIH Certificate of Confidentiality Application Instructions |
| Protocol Application Form Instructions | New | |||
Protocol Application Form |
Word | New | ||
Repository Application |
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Record Review Form |
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Exemption Request |
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Not Human Subjects Research Form |
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REQUESTS FOR RENEWALS AND CLOSURE:
Instructions for Request to Reapprove a Research Study |
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Reapproval Request |
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Closure Request |
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AMENDMENTS:
Amendment to Change Principal Investigator |
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Amendment to Add or Remove Investigator(s) and Study Personnel |
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Amendment to Protocol or Associated Documents |
Word |
EMERGENCY USE, ADVERSE EVENTS AND DEVIATIONS:
Emergency Use Report |
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Emergency Use Consent Form |
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Report of Adverse Event(s) under Yale PI (Form 6A) |
Word | ||
Report of Adverse Event(s) under Non-Yale PI (Form 6B) |
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Protocol Deviation/Unanticipated Problem Report Form |
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Lost/Stolen Laptops Form |
Word |
OTHER:
| HIC Protocol-Related Conflict of Interest Disclosure Form |
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Request for Permission to Serve as Principal Investigator on a Research Protocol Involving Human Subjects |
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Collaborating Investigator Instructions |
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Request for Permission to Serve as a Collaborating Investigator |
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TISSUE AND SPECIMEN REQUESTS:
Summary Sheet for Pathology Department Tissue |
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Requests for Research Use of Human Specimens |
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Yale New Haven Hospital Request for Excess Clinical Samples |
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Cancer Data Repository (CaDR) |
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| HIC Institutional Endorsement of Proposed Research Involving Human Subjects (Form 10) |
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| Terms of the Federalwide Assurance Office for Human Research Protections (OHRP) Web site |
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Templates Templates are now available online and should |
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| Data and Safety Monitoring Template |
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Consent Forms: |
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Informed Consent Template | ||
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Informed Consent Template - Spanish Version |
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Compound Authorization Form | ||
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Child Assent Form Template |
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| Repository Consent Template | |||
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Authorization for Donation of Excess Tissue | ||
| Authorization and Advanced Directive | |||
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Consent to Filming or Video-taping for Research Purposes |
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| Consent Addendum | |||
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Checklists |
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| Informed Consent Checklist |
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| Checklist for Banking of Data and Biologics for Future Use |
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Last modified: Thursday, 14-Aug-2008 17:03:37 EDT (JP)