IRB/RAB Forms | IRB/RAB

IRB/RAB

Assurance of Compliance

	Name	Description	Status	Source
	IRB Registration Valid Through 4.9.2028		Required	IRB Registration IORG0000481 through 4.9.2028.pdf	Edit IRB Registration Valid Through 4.9.2028	Delete IRB Registration Valid Through 4.9.2028

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IRB Operating Code and Clinical Research Policy Manual

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	Name	Description	Status	Source
	Clinical Research Policy Manual - IRB		Required	Clinical Research Policy Manual 2017.pdf	Edit Clinical Research Policy Manual - IRB	Delete Clinical Research Policy Manual - IRB
	IRB Operating Code		Required	Institutional Review Board - Operating Code Suggested Edits updated 8.5.2024.pdf	Edit IRB Operating Code	Delete IRB Operating Code

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Institutional Review Board (IRB)

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Name	Status	Source
New Protocol Application Form	Required	02 New Protocol Application Form - 2.8.21.docx	Edit New Protocol Application Form	Delete New Protocol Application Form
Human Research Protection Education Training PI Investigator	Required	03 Human Research Protection Education Training PI.docx	Edit Human Research Protection Education Training PI Investigator	Delete Human Research Protection Education Training PI Investigator
Research Team Attachment	Required	04 Research Team Attachment - Jan 2021.docx	Edit Research Team Attachment	Delete Research Team Attachment
PI responsibility form	Required	05 PI responsibility form - Jan 2021.docx	Edit PI responsibility form	Delete PI responsibility form
IRB - Consent Form Template	Required	06 IRB - Consent Form Template - Jan 2021.docx	Edit IRB - Consent Form Template	Delete IRB - Consent Form Template
Biomedical Research Consent Template	Required	06a Biomedical Research Consent Template - Jan 2021.docx	Edit Biomedical Research Consent Template	Delete Biomedical Research Consent Template
Biomedical Research Consent Template Additional	Required	06b Biomedical Research Consent Template Additional.docx	Edit Biomedical Research Consent Template Additional	Delete Biomedical Research Consent Template Additional
Subjects PHI Authorization Form	Required	08 Subjects PHI Authorization Form - Jan 2021.docx	Edit Subjects PHI Authorization Form	Delete Subjects PHI Authorization Form
Appendix A - Research Equipment Form	Required	13 Appendix A Research Equipment Form - Jan 2021.docx	Edit Appendix A - Research Equipment Form	Delete Appendix A - Research Equipment Form
Appendix B1 - Device Form	Required	09 Appendix B1 Device Form - Jan 2021.docx	Edit Appendix B1 - Device Form	Delete Appendix B1 - Device Form
Appendix B2 - Drug and Chemical Usage Form	Required	11 Appendix B2 Drug and Chemical Usage Form - Ja.docx	Edit Appendix B2 - Drug and Chemical Usage Form	Delete Appendix B2 - Drug and Chemical Usage Form
Appendix C - Biological Materials Form	Required	10 Appendix C Biological materials form - Jan 20.docx	Edit Appendix C - Biological Materials Form	Delete Appendix C - Biological Materials Form
Local Contextual Review	Required	12 IRB Local Contextual Review - Jan 2021.docx	Edit Local Contextual Review	Delete Local Contextual Review
Research Insurance Coverage protocol	Required	14 Research Insurance Coverage protocol - Jan 20.doc	Edit Research Insurance Coverage protocol	Delete Research Insurance Coverage protocol
IRB termination form	Required	15 IRB termination form.docx	Edit IRB termination form	Delete IRB termination form
Required Product Information	Required	07 Required Product Information - Jan 2021.docx	Edit Required Product Information	Delete Required Product Information

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IRB/RAB

Assurance of Compliance

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IRB Operating Code and Clinical Research Policy Manual

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Institutional Review Board (IRB)

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Informed Consent

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Adverse Event/Protocol Deviation

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