For investigators & research personnel
	IRB mission
	Assurance of Compliance
	RSPP guidance documents
	IRB forms
	Informed consent templates

Quality Assurance/Quality Improvement vs. Research

	Conflicts of Interest in Research
	Honest Broker Requests
	Nursing Research
	Humanitarian Use Devices (HUD)
	NCI CIRB submissions
	Emergency Use of Investigational (Experimental) Articles
	IRB meeting schedule & deadline for submission
	Regulations & guidance governing human subject research
	Research privileging
	Research compliance training
	Education & training in human subjects protection
	Community information
	Other useful links
	Mailing information
	RSPP staff
	IRB chairs
	IRB member rosters
	Contact us
	Return to the IRB home page

Other useful links

• Aurora Clinical Research Department
• Aurora Continuing Medical Education
• Expedited Review Categories
• Food and Drug Administration (FDA)
• FDA Forms - Drugs
• FDA Forms - Devices
• FDA IRB and Investigator Information Sheets
• Glossary of Lay Terms for use in Preparing Consent Forms for Human Subjects
• National Institutes of Health (NIH)
• Office for Civil Rights - HIPAA
• Office for Human Research Protections (OHRP)
• Office of Research Integrity (U.S. Department of Health and Human Services)

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