Rave EDC is the cornerstone of the Medidata Rave Clinical Cloud, offering you fast implementation and maximum control to support studies of any size, length, or complexity. Rave EDC is proven by more than 17, studies one-third ongoing today and more than 4 million patient experiences. Our flexible architecture empowers clinical research teams to capture, cleanse, and manage study data, ensuring efficient trial execution across every phase of the clinical trial life cycle. You can even collect data across clinical and non-clinical sources and easily integrate it with Rave EDC. Boost productivity by using Rave EDC tools for collaboration with one instance for all roles.
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Study teams are facing fewer resources, tighter timeframes and smaller budgets, while coping with exponential increases in data, complex study endpoints, and more sites. Managing activities and information across multiple, disparate systems is cumbersome, time-consuming, and can lead to mistakes. With fewer resources to drive team effectiveness and study outcomes, you need a CTMS that cuts through these rising complexities of clinical trial management and Medidata has the solution.
Rave CTMS is the only data-driven solution for faster, smarter, end-to-end trial management. Collapsing operational silos and enabling study team collaboration, Rave CTMS centralizes data and processes in a shared environment for a single source of truth.
This transforms data into context and delivers alerts to proactively identify and remedy issues before they become problems. Rave CTMS dramatically streamlines, accelerates and improves trial management, while ensuring regulatory compliance and inspection readiness.
Actuals vs. Forecast The only data-driven CTMS tracking and reporting that delivers real-time contextual insights for proactive issue management. End-to-end transparency In one view, all stakeholders see data and performance metrics on enrollment, visit reports, milestones, and issues.
Always inspection ready Safeguard and speed up submission readiness and automated reporting at any point of your study. Higher compliance Management of issues meeting compliance requirements from first visit to study close. Prioritizing onsite activities Enable cross functional information for faster and earlier remediation of issues.
Increased CRA productivity Advanced visit scheduling based on risk level rather than one study schedule. Faster assessments, training, monitoring, closeout, and document management on one platform. Smarter supply management Greater control over drug supply forecasting and inventory management. Always compliance ready Better adherence to the study protocol and regulations with the ability to digitize ISF completion process. Proactive remediation Monitor and manage inclusion and exclusion criteria.
Alert always on Immediately alerted to review issues arising around protocol or study design. No mistakes Enter data once to seamlessly populate it across other applications.
Eliminate inconsistent data integration and data entry duplication. Clear and simple Centralized administration with role-based permissions. Highest productivity Single environment to capture, manage, aggregate, and access all data clinical and non-clinical. Real-time data power Data access and analytics for coding, safety management, and insight-based decisions. Accelerated studies Faster study start-up, database build, data cleaning, and database lock.
Audit ready Auditable data with the most comprehensive list of leading certifications. Faster deployment Single, scalable, and out of the box integration with other Rave applications. EDC agnostic. Simple set up, implement, and upgrade. Better experience Consistent user experience with a single sign-on. No longer will we have excel trackers, and specialized reports, that someone else is creating. Nick Dyer Chief Executive Officer. We may use both session cookies which expire once you close your web browser and persistent cookies which stay on your computer or mobile device until you delete them to provide you with a more personal and interactive experience on our Site.
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IT Audit ready Auditable data with the most comprehensive list of leading certifications. Quiet the data noise to make informed decisions with visualizations and reports. Drive transparency for collaboration. Transform any data into context to enable visualization to drive better decisions.
User-focused on data review and action orientated activities. Predictive data capture for complete oversight early and unique insight. Break down workflow and data silos with one integrated solution; a single source of truth across all stakeholders. Efficiently manage the entire study with data automatically populated from any EDC for dashboards, forecasts, and analysis.
Eliminate redundancies with a single source of data truth. Prioritize safety and patients by eliminating administrative tasks easily addressed with technology. Robust data engine connected to one standardized data repository. Improved use of central and distributed study team resources. Clear indicators predicting and quantifying possible deviations. Centralized issue management for proactive remediation across stakeholders. Timely data to ensure you stay the course. Optimized processes and effective resource allocation.
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Designed as a unified data platform, the Rave Clinical Cloud creates a single source of truth for all study-related data. Simply put, enter data once and let the platform master and populate it throughout the end-to-end suite of Rave applications. Optimize operational execution, decrease the data entry and maintenance burden, and reduce the number of clinical systems across your study teams. Throw away your list of passwords and excel sheets, you are now on a truly unified platform.
The Medidata Rave Clinical Cloud
Rave RTSM has been built to support Clinical Supply Managers by making it easier to handle shipments and track devices by providing more robust features and reporting capabilities. Even more, Rave RTSM supports Data Managers and Clinical Operations managers by seamlessly integrating with Rave EDC to eliminate duplicate data entry, reduce reconciliation, decrease administrative burden associated with traditional methods of specifications, and significantly lower your risk and cost. Rave RTSM is completely configurable with pre-validated components so you can get your study started faster. Coupled with supply integration service, on-demand shipping, and robust reporting, end users can experience a comprehensive RTSM solution. With Rave RTSM, you can start your study in two to three weeks versus the industry standard of six-plus weeks. Rave RTSM offers unrivaled flexibility for your trial. Make mid-study changes in real time, without time-consuming change orders.
Study teams are facing fewer resources, tighter timeframes and smaller budgets, while coping with exponential increases in data, complex study endpoints, and more sites. Managing activities and information across multiple, disparate systems is cumbersome, time-consuming, and can lead to mistakes. With fewer resources to drive team effectiveness and study outcomes, you need a CTMS that cuts through these rising complexities of clinical trial management and Medidata has the solution. Rave CTMS is the only data-driven solution for faster, smarter, end-to-end trial management. Collapsing operational silos and enabling study team collaboration, Rave CTMS centralizes data and processes in a shared environment for a single source of truth. This transforms data into context and delivers alerts to proactively identify and remedy issues before they become problems. Rave CTMS dramatically streamlines, accelerates and improves trial management, while ensuring regulatory compliance and inspection readiness.