Enable clinical study partners to streamline information sharing across clinical trials. Vault Site Connect provides visibility and automated collaboration between sponsors and sites, including document exchange, safety letter distribution, and subject status helps to accelerate trials, ultimately getting products to patients faster.
Seamlessly automate the flow of information across study partners, processes, and systems to speed trials.
Sites spend less time on administrative activities to focus on treating patients, improving collaboration, and efficiency.
Eliminate manual processes and gain real-time visibility of information throughout trial operations to improve quality and inspection readiness.
Clinical documents are automatically shared across Vault Clinical and SiteVault to reduce manual steps associated with sponsor TMF and site eISF reconciliation activities.
Easily manage and distribute site document packages during study initiation to speed study start-up.
Guarantee delivery and tracking of important safety letter information sent to sites so that principal investigators stay informed.
Import, distribute, and track completed CRF output from EDC to clinical research sites, including auto-filing in eTMF and eISF.
Deliver payment letters to clinical research sites using SiteVault and receive site invoices directly within Vault Clinical.
Eliminate the need to manage external site accounts in your sponsor Vault with SiteVault Free, a compliant eISF application for sites. Training and support are provided by Veeva, so that you can focus on higher-value engagement with your sites.
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