Eight Parameters to Achieve Site- and Patient-Centric Decentralized Trial Capabilities
Disruptions preventing or limiting clinical trial site access to patients, monitors, and CRAs are propelling long-lasting changes in the research industry, supported by the adoption of trial virtualization technologies. The urgency to adapt to evolving requirements for both patients and sites is prompting sponsors to engage in new discussions with their CROs.
This guide provides eight parameters to help sponsors optimize their path to virtualization across key site- and patient-centric capabilities.
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