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eSRA is a common tool across sites and sponsors for assessing the readiness of site systems to be used in the conduct of regulated clinical trials
This document is intended to provide information (in addition to the eSRA Handbook) to sponsors/CROs in deciding to implement eSRA for evaluating a site system’s readiness to provide regulatory-acceptable data and documents for their clinical trials.
Japanese Translation: eSRA Handbook and Assessment Forms V2026
の日本語版2025.2JP1が2026年6月02日にリリースされました。
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