Accurately and efficiently randomizing patients and supplying treatments is at the very heart of clinical trials. When managing these deeply connected RTSM processes, why use clunky, outdated, bolted together systems? Medidata Balance is a unique RTSM solution within the Medidata Clinical Cloud.Learn more
Although a necessary part of every trial, Medical Coding adds to study timelines and increases costs. Medidata Coder helps you code faster and more consistently across all trials - even those using different EDCs - working seamlessly with Rave (EDC), integrating with non-Rave systems, and helping to centralize and streamline the medical coding process.Learn more
Monitoring and reviewing clinical trial data is critical for any clinical development plan. But today’s manual processes often result in errors, compromising data quality and incurring costly study delays.
Medidata Centralized Statistical Analytics (CSA) provides immediate insight into site performance and data quality, making it easier to detect and track critical changes throughout the trial. CSA also integrates data from different systems and provides a comprehensive report for each subject.Learn more
Your clinical trial management system (CTMS) should adapt to you, not vice versa. That’s why Medidata CTMS was created in the cloud more than 10 years ago—with powerful modules for outsourcing, site monitoring and site payments you can access together, or separately, as needed.Learn more
Can you tell if you're overpaying for procedures? Is site budgeting slow and contentious? It’s time for a change.
Medidata Grants Manager transforms site budgeting and negotiation to save both money and time.Learn more
Technology should make our lives easier, not create bottlenecks, delay study starts and burden sites and sponsors with potentially dozens of URLs, usernames and passwords. Medidata alleviates all of that with iMedidata, a fast, simple and secure portal to access all of your studies, eLearning courses, and centralized user administration.Learn more
With the right information and analytics, it’s possible to make better clinical development decisions to minimize cost, cycle time and risk.
Medidata Insights is the turnkey clinical analytics solution that provides advanced metrics, visualizations and the most reliable set of industry data and benchmarks.Learn more
The use of medical imaging in clinical trials is growing rapidly. Roughly 50% of all trials use medical imaging as an endpoint, or for eligibility criteria. In therapeutic areas like oncology, nearly all trials rely on medical imaging.Learn more
A monitoring solution wouldn’t be complete without the tools that clinical research associates (CRAs) need to efficiently manage site monitoring activities and create visit reports.
Medidata’s cloud-based on-site monitoring module is integrated with EDC—providing smart workflows and structured visit reports that pull data directly from EDC to save CRAs time and improve the quality of data and documents.
Medidata Operational Performance Analytics (OPAL) is the only turnkey executive dashboard with operational insights that help life science companies accelerate treatments to market. By benchmarking against the largest store of clinical trial data, OPAL illustrates how organizations perform relative to their peer group, and provides an at-a-glance view of quantitative, objective metrics down to the audit level.Learn more
Medidata Patient Cloud® is a comprehensive and regulatory compliant mobile health (mHealth) solution that accelerates patient-centric clinical research. Patient Cloud enables sponsors to use sensors and apps that capture a richer, more complete dataset directly from the patient, improving the clinical trial experience on the Medidata Clinical Cloud.
Patient Cloud provides a clearer, more nuanced picture of a therapy’s safety and efficacy, incorporating technologies for patient data capture and services that help propel mHealth studies.Learn more
The Medidata Payments Cloud automates the clinical site payment workflow. It processes high volumes of invoices and complex payment requests to sites across the globe quickly and accurately. Whereas sites can sometimes wait months for reimbursement, Payments significantly improves the timetable, thus helping ensure and preserve the site-sponsor/CRO relationship.Learn more
There’s nothing more important than patient safety, yet paper-based processes for adverse events (AEs) and serious adverse events (SAEs) are laborious and error-prone. At best, they drive up study cost. At worst, they put patients at risk.
Conversely, Medidata Rave Safety Gateway automates AE and SAE collection via a secure, configurable electronic transmission interface between Rave and E2B-standard safety systems.Learn more
Medidata RaveX is the world’s leading solution for capturing, managing and reporting patient data, including unified EDC, CDMS and lab administration features. RaveX is the cornerstone of the Medidata Clinical Cloud, allowing you to seamlessly add Medidata’s randomization, trial supply, medical coding, safety reporting and mHealth capabilities as your organizational needs grow.Learn more
Are you launching a risk-based monitoring (RBM) study? You don’t need to blaze the trail. With Medidata RBM, design and conduct any RBM program in real time. Medidata RBM is comprised of cloud technology and strategic consulting services so you can quickly realize the quality, cost and timeline benefits of RBM.Learn more
Poorly designed studies severely impact downstream clinical trial execution. Excessive procedures that hurt patient enrollment and retention, mistakes that drive costly protocol amendments, and up-front trial design problems continue to have a negative impact.
Medidata Study Design Optimization service optimizes your clinical trial design for a dramatically better operational execution.Learn more
Can you quickly identify which investigator sites are capturing accurate clinical data from patients, and those that aren’t? If you're relying on anecdotal information or past performance records, probably not.
Medidata SQM alerts your study team to quality changes at sites while your study is still in progress.Learn more
Targeted Source Document Verification (TSDV) devours more than 15 percent of trial budgets. Yet research shows that verifying every data point does not significantly improve data quality. Instead, what if you could automatically target SDV where you need it most?
Medidata TSDV lets you reduce SDV coverage without sacrificing data quality or regulatory compliance.Learn more
Patient safety and data integrity are critical to a successful clinical trial. Increasing trial complexity and globalization have made monitoring and reviewing data ever more challenging.
Medidata Trial Assurance evaluates the integrity and quality of a trial’s clinical and lab data, with patent-pending statistical algorithms that mine the clinical database automatically to identify anomalies, outliers, potential fraud, misconduct and/or procedural issues.Learn more