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Autumn M Eberly
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1.6 IRB Composition, Leadership, Qualifications, and Responsibilities
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Autumn M Eberly
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
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2 years ago
Autumn M Eberly
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
2 years ago
2 years ago
Autumn M Eberly
User for 4 years
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
HRPP Policies and Procedures
Section 6: FDA Regulated Research/Drugs...
1.0 Purpose 1.1. The purpose of this policy and procedure is to describe the requirements for ut...
Table of Contents
HRPP Policies and Procedures
Section 1: General Human Research Protection Program Polices 1.1 Human Research Protection Progr...
8.7 Reporting Incidents to Institutional Officials and Federal Agencies
HRPP Policies and Procedures
Section 8: AEs, Unanticipated Problems ...
1.0 Purpose The purpose of this policy is to describe the Organization’s requirements to ensure ...
8.6 Study Hold, Suspension, and Termination
HRPP Policies and Procedures
Section 8: AEs, Unanticipated Problems ...
1.0 Purpose The purpose of this policy is to describe the process for study holds, study suspens...
8.5 Noncompliance by the IRB or Other Components of the HRPP
HRPP Policies and Procedures
Section 8: AEs, Unanticipated Problems ...
1.0 Purpose The purpose of this policy is to describe the process for reviewing and reporting in...
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