Forms and Templates

Forms, templates, and worksheets from the Office of Research.

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Type All Applications / Forms Agreement Checklist / Matrix Executive Order External Page or Resource GIM / Policy Manuals Media Fact Sheet Procedures & Guidance Report Stats and Rankings Templates / Worksheets Tool (SAGE, MyResearch, etc) Training Course Materials (Required training or CORE courses)

Subject All Artificial Intelligence Assent Assurance Budget Extensions, No-Cost Extensions CITI Registration Clinical Trials Compassionate Use Consent Controlled Information Categories for Classified or Restricted Research Delayed Onset Human Subject Research Department of Defense Department of Energy Department of Justice Device Emergency Use Devices Drug or Biologic, Emergency Use Drugs, Biologics, Botanicals Electronic Consent Emergency Medicine Emergency Use End of Award Engagement Environmental Protection Agency eSignature, eConsent Exemption Expedited Review Export Control External IRB F&A Waiver Faculty Reduced Responsibility Status Involving External Funding FDA, Drugs, IND Requirements FDA, IDE Requirement Genomic Data Sharing HIPAA Authorization Human Subjects Assistance Program Human Subjects Research Human Subjects Training Intellectual Property IRB Application IRB Review Join an IRB Local Context Multi-site or collaborative research Multi-Site Research, Collaborative Research Mutual Non-Disclosure Agreement Sample Neonates New Subrecipient Entity Certification New Subrecipient Entity Certification - Domestic Subrecipients New Subrecipient Entity Certification - Foreign Subrecipients OSP/GCA Modification Checklist Pregnant Women Prior Approval Prisoners Report of New Information Research with Children Signature Delegation Single IRB Status Report Subaward Monitoring Translation, Consent Forms

Owner All HSD ORC ORIS OSP GCA

Media type	Name	Updated	Subject	Owner	Download
	WORKSHEET Pre-Review, Modification	09/25/2025		HSD
	Human Subjects Division Organizational Chart	09/15/2025		HSD
	WORKSHEET Engagement	08/29/2025	Engagement	HSD
	WORKSHEET Human Subjects Research Determination	08/29/2025	Human Subjects Research	HSD
	*IRB Protocol, No Contact with Subjects	08/29/2025	IRB Application	HSD
	*Request External IRB Review	08/29/2025	External IRB	HSD
	Emergency Use, Drug or Biologic Notification	08/29/2025	Drug or Biologic, Emergency Use	HSD
	Multi-site or Collaborative Research Supplement	08/29/2025	Multi-Site Research, Collaborative Research	HSD
	*Separate Key Information Consent Template (more than 2,000 words)	08/29/2025	Consent	HSD
	*No Separate Key Information Consent Template (2,000 words or less)	08/29/2025	Consent	HSD