Equip sites and patients with the tools they need to accelerate and improve screening and onboarding.
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Responsive omnichannel interfaces with pixel-perfect, role-specific workflows for patients, sites, CROs, and sponsors
Custom screening logic and site routing based on the protocol and active sites for any given trial
Instantaneous patient access to medical records from one or multiple providers, as well as nationwide health information exchanges
Automatic mapping of patient medical history to trial inclusion/exclusion criteria to flag potential eligibility issues
Efficient integration and data exchange with existing systems (e.g., EDC, CTMS) and third-party services (e.g., clinical data, virtual connectivity, eConsent)
Monitoring and alerts as to each site’s real-time performance against recruitment targets and whether or not they are on track
Even before COVID-19 prompted an unprecedented rush for new vaccines and therapeutics, it was clear that many existing clinical trial processes were technologically outmoded. Now that the world is depending on the life sciences industry to lead the way out from this pandemic, the need to move away from in-person engagements, on-site monitoring, paper documentation, and other manual checkpoints has taken on a new urgency.
