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Harness Site-based eISF Platforms to Accelerate Clinical Operations

Learn how sponsors and CROs use remote site access, start-up, monitoring, and SDV to optimize clinical trial processes.

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Clinical trial success depends on the sponsor or CRO's ability to collaborate across different study sites. But disjointed methods like on-site visits, email communication, and clunky FTP portals make it difficult for sponsors and CROs to store and exchange documents. 

With so many study sites coming online, sponsors and CROs are uniquely situated to turn on helpful features like remote site access, monitoring, SDV, oversight, management, collaboration, and document and data exchange through eISFs.