Viedoc

Viedoc provides a browser-based eClinical platform led by EDC, with ePRO/eCOA, eTMF, randomization and trial supply management, televisits and medical coding, plus study build services and integrations with other study systems. It reports 8,000 studies in more than 75 countries.

Clinical Data and Study Operations

• Capture study data and configure eCRFs, workflows, and real-time edit checks with Viedoc EDC and Viedoc Designer.
• Collect patient-, clinician-, and observer-reported outcomes through ePRO, with reminders, audit trails, and real-time EDC data flow.
• Cut coding time with AI-assisted medical coding in Viedoc Coder, with every code approved by the client's team.

Monitoring, Analytics, and Documentation

• Plan targeted source data verification by site risk and time period with Viedoc SDV Manager, while retaining an audit trail of coverage.
• Monitor enrollment, queries, site performance, and data quality through built-in dashboards; manage controlled study documents in Viedoc TMF.

Integrations, Dashboards, and Long-Term Studies

• Connect Viedoc to other study systems, such as a CTMS or SAS LSAF, through its integration service.
• Support longitudinal patient-data collection for long-term observational studies and view adverse-event monitoring through dashboards, reports, and alerts.

Trial Supply and Distributed Participation

• Manage treatment allocation, kit types, stock thresholds, expiry, and site-level inventory with Viedoc Logistics and Randomization software.
• Support decentralized and hybrid study workflows through integrated EDC, ePRO, and Televisits, with participant reminders for scheduled activities.

Best Fit

• Best suited to clinical research teams seeking a software platform for study data capture, participant outcomes, monitoring, documentation, and trial supply.
• Also fits sponsors and study teams that need integrations with their other study systems, operational trial dashboards, or software for long-term observational data collection.