Medidata Rave EDC
Clinical Trial Management Software
Medidata Rave EDC serves as the central hub for your clinical trial data, allowing you to capture, manage, and report on patient information with h
Viedoc is a unified eClinical solution designed to accelerate clinical trials through integrated electronic data capture, trial management, and real-time data monitoring for life science researchers.
Main Demo Video
Viedoc provides a unified platform to manage every stage of your clinical trials, from initial study design to final data reporting. You can replace fragmented systems with a single interface that handles electronic data capture (EDC), clinical trial management (CTMS), and electronic trial master files (eTMF). This integration helps you maintain data integrity while reducing the time spent on manual data entry and reconciliation across different providers.
The platform is built to scale with your research needs, whether you are running a small early-phase study or a complex global trial. You can manage patient-reported outcomes directly through mobile devices and use built-in coding and logistics tools to keep your study on track. By centralizing your clinical operations, you gain better visibility into trial progress and can make faster, data-driven decisions to bring new treatments to market.
Main dashboard with project overview
Kanban-style task management
Gantt chart timeline view
Workflow automation builder
Stop struggling with disconnected clinical tools. Viedoc offers a suite of integrated modules that let you design, manage, and analyze your studies in one secure environment.
Capture and manage clinical data efficiently with an intuitive interface designed for site investigators and data managers.
Build your entire study workflow visually, including complex validation rules and forms, without needing advanced programming skills.
Collect data directly from patients using their own devices to improve engagement and ensure high-quality primary outcomes.
Manage your clinical supply chain and track investigational products from the warehouse to the patient in real-time.
Maintain a complete and compliant electronic trial master file with automated document filing and easy inspection readiness.
Monitor your trial performance with visual dashboards that highlight recruitment trends, data queries, and site productivity.
Viedoc uses a project-based pricing model tailored to the specific complexity and duration of your clinical trial. You won't find a one-size-fits-all subscription, as costs depend on your study's scale and required modules. You can request a personalized quote or a guided demo to see how the platform fits your budget and research goals.
Based on feedback from clinical researchers and data managers, here is how Viedoc performs in real-world trial environments:
Perfect for pharmaceutical companies, CROs, and academic researchers who need a unified, compliant platform to manage mid-to-large scale clinical trials.
Viedoc is a top-tier choice if you want to move away from clunky, legacy clinical trial systems. Its biggest strength lies in its modern, user-friendly design which significantly lowers the barrier for site staff and patients to enter high-quality data.
While you will need to contact sales for a custom quote, the efficiency gained during study setup and data cleaning often offsets the lack of transparent pricing. Highly recommended for clinical operations teams who prioritize a unified workflow and need to maintain strict regulatory compliance without sacrificing speed.
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Main dashboard with project overview