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 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 Children	12/23/2024	Research with Children	HSD
	*IRB Protocol, No Contact with Subjects	12/23/2024	IRB Application	HSD
	Other REDCap Installation Supplement	12/23/2024	Electronic Consent	HSD
	*No Separate Key Information Consent Template (2,000 words or less)	12/23/2024	Consent	HSD
	Diversity Plan for Clinical Trials Supplement	12/23/2024
	WORKSHEET Pre-Review, Initial Application	01/30/2025		HSD
	Cloud Computing Use Statement	02/20/2025		OSP
	CHECKLIST: OSP & GCA Modifications in SAGE	02/21/2025	OSP/GCA Modification Checklist	OSP
	Non-UW Individual Investigators Supplement	02/27/2025	Multi-site or collaborative research	HSD
	WORKSHEET Pre-Review, Continuing Review	02/27/2025		HSD