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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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Autumn M Eberly
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
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Autumn M Eberly
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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 and procedure is to describe the IRB’s authority to: a) a...
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 and procedure is to describe the: 1) definitions and clas...
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