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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 2018-02-08

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: 629173

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

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