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Part 1 of 3 Part Series: Part 1 of 3 Part Series:

Part 1 of 3 Part Series: - PowerPoint Presentation

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Uploaded On 2017-05-19

Part 1 of 3 Part Series: - PPT Presentation

Informed Consent The Document Wendy Lloyd BA LPN CIP CCRP Regulatory Affairs and Compliance Specialist Process Improvement Team Agenda Identify consent document requirements Distinguish between IRB PI and Coordinators consent document responsibilities ID: 549955

subject consent irb research consent subject research irb document fda subjects informed study elements http www gov documents information procedures participation ohrp

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