Forms and Templates

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

Search

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
	Assent Template	01/30/2015	Assent	HSD
	Clinical Trial Registration Work Flow	02/13/2017	Clinical Trials	HSD
	WORKSHEET Clinical Trial Registration	05/11/2017	Clinical Trials	HSD
	Consent Requirements and Expectations for Genomic Data Sharing	05/11/2017	Genomic Data Sharing	HSD
	CITI DON Course Registration Instructions	12/10/2018	Human Subjects Training	HSD
	WORKSHEET Expedited Review	08/26/2021	Expedited Review	HSD
	Delayed Onset Human Research (DOHR) Determination Request	10/08/2021	Delayed Onset Human Subject Research	HSD
	TEMPLATE Translation Attestation	10/08/2021	Translation, Consent Forms	HSD
	Exception from Informed Consent for Emergency Research (EFIC) Supplement	10/28/2021	Emergency Medicine	HSD
	WORKSHEET IRB Review Outcomes	12/28/2021	IRB Review	HSD