DOCUMENT ID	DOCUMENT TYPE	TITLE	VERSION #
HRP-2600	GUIDANCE	Activities That are Not Human Subjects Research	1.0
HRP-2601	GUIDANCE	Expanded Access to a Test Article	1.0
HRP-2630	GUIDANCE	Modifications to Exempt Research	1.0
HRP-2631	GUIDANCE	Types of Reportable New Information and their Reporting Requirements	1.1

HRP-2730	FLOWCHART	Decision Tree for Reporting New Information	1.0
HRP-2731	FLOWCHART	Decision Tree for Determining Use of Individual Investigator Agreement vs IRB Authorization Agreement	3.0

HRP-2350	AGREEMENT	Individual Investigator Agreement	3.4
HRP-2351	AGREEMENT	Single Study IRB Authorization Agreement	1.0

HRP-2650	INFORMATION	Exempt Research Categories	1.0
HRP-2651	INFORMATION	Research Categories Eligible for Review by the Expedited Procedure	1.0
HRP-2652	INFORMATION	HIPAA Data Guidelines	2.0
HRP-2653	INFORMATION	Criteria for IRB Approval of Research	1.0
HRP-2654	INFORMATION	Registering a Study at ClinicalTrials.gov	1.1
HRP-2655	INSTRUCTIONS	Supplemental Instructions for Consent Form	1.0
HRP-2656	INSTRUCTIONS	Instructions for Short Consent Forms	1.2
HRP-2660	INFORMATION	Examples of Non-compliance & Serious Non-compliance	1.1
HRP-2661	INFORMATION	Examples of Adverse Events that are Unanticipated Problems	1.0
HRP-2662	INFORMATION	Examples of Adverse Events that are Not Unanticipated Problems	1.0
HRP-2663	INFORMATION	Examples of Non-adverse Events that are Unanticipated Problems	1.0
HRP-2670	INFORMATION	LSUHSC Local Context Questionnaire Information	1.0
HRP-2672	INFORMATION	Non-HSC Research Personnel Training and Documentation Requirements	1.0
HRP-601	DATABASE	IRB Roster	1.0

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