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Implementing eSRA: Sponsor Perspective

This document is intended to provide additional information to sponsors in deciding to implement eSRA for evaluating site system’s readiness to provide regulatory-acceptable data for their clinical trials. It includes a mapping of eSRA questions to statements from regulatory authority documents.

This document is intended to be used in conjunction with the eSRA Handbook and Questionnaire.

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Categories: Regulatory, eSRA, Visible by Public, PUBLIC DOWNLOADS, ReportNumber of views: 2113

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