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Uploaded On 2016-05-09

Tool: - PPT Presentation

Sponsor Responsibilities Based on ICH E6 GCP Guidance Section 5 Purpose To provide an overview of Sponsor Responsibilities to study sites AudienceUser NIDCR study staff including PIs SubIs and Site ID: 311983

trial ich sponsor monitoring ich trial monitoring sponsor regulatory data protocol investigator written clinical requirements investigators study responsibilities information

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