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Research Service Programs
Clinical Trials Office (CTO)
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Direct Access: LSUHSC Researchers & Staff
Direct Access: LSUHSC Researchers & Staff
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Office of Research Services
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OTHER DOCUMENTS
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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