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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.
eCF Spring 2026 Workshops Announced!
We are happy to announce our Spring workshops!
Europe/Hybrid: Hosted by Servier outside of Paris on April 14-16 (this will be livestreamed as well)
Americas: Hosted by YPrime outside of Philadelphia, PA on April 28-30
Asia: Hosted by Novartis in Tokyo, Japan on April 2-3