IRB Submission Receipts

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Tips On Informed Consent

Sample Consent Document Language

Full Board Review

Today is Tuesday, October 7th 2008

Available Forms:

Application for New Protocol Review

Supplements for Application for New Protocol Review

Exemption from IND/IDE Checklist

Application for Continuation

Application for Approval of Amendment

Application for Study_Personnel & Site Changes

Application for Exemption from Review

Application for Final Study Closure

Reportable Events Form

Notification of Emergency Use Form

IRB Drop off Receipts

Application for
waiver of Authorization/Consent

Application for
Treatment IND/IDE

IRB Submission Receipt

IRB Drop off Receipt

All receipts are available in MS Word format.

IRB Resources
	Research Team Required Human Subject Protection Education
	Decision Charts - Human Subject Regulations Decision Charts
	IRB Newsletter
	IRB Course Calendar
	Policies and Procedures
	HELP Downloading Forms
	Lay Glossary
	Useful Web Links
	Sponsored Programs Administration (SPA)
	Office of Clinical Trials (OCT)
	Email a Suggestion or Comment to the IRB
	Contact the IRB
	GCRC Web Page
	Instructions for Research Conducted at Bellevue
	HRPP Accreditation Tutorial for informational purposes only
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