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Autumn M Eberly
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1.6 IRB Composition, Leadership, Qualifications, and Responsibilities
3 years ago
3 years ago
Autumn M Eberly
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
3 years ago
3 years ago
Autumn M Eberly
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
3 years ago
3 years ago
Autumn M Eberly
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6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use
1.0 Purpose 1.1. The purpose of this policy and procedure is to describe the requirements for ut...
Table of Contents
Section 1: General Human Research Protection Program Polices 1.1 Human Research Protection Progr...
8.7 Reporting Incidents to Institutional Officials and Federal Agencies
1.0 Purpose The purpose of this policy is to describe the Organization’s requirements to ensure ...
8.6 Study Hold, Suspension, and Termination
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
1.0 Purpose The purpose of this policy is to describe the process for reviewing and reporting in...
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