Rave Clinical Operations

Drive Faster Clinical Trial Decisions with Data

Data first drives everything we do at Medidata. We enable optimized clinical trial operations by surfacing actionable data insights to target and focus study team activities. We achieve this through our 10+ year investment in Data Science, embedding powerful analytics where they are needed most – within core clinical operations workflows – bringing insight directly to the frontlines of decision-making.

Improve Clinical Trial Oversight

The growing complexity of the clinical trial ecosystem highlights the need to maintain continuous oversight at both the study and program level. Regardless of the outsourcing model, organizations need to manage trial risk, site performance, data integrity, and regulatory compliance. True oversight goes beyond visibility: it provides the power to remediate issues in time to avoid trial delays. Medidata delivers holistic, truly digital oversight through coordinated capabilities built on aggregated data.

Connect Users Across the Clinical Trial Lifecycle

As the functional silos within clinical teams break down, so too must the boundaries between clinical technologies break down. From trial planning through execution, Medidata provides a single data ecosystem for users to interact across capabilities. Now your teams across clinical operations, data management, monitoring, risk management, and finance all have a common environment to communicate with each other, complete workflows bridging across applications, and foster collaboration across their teams.

Accelerate the New Generation of Decentralized Clinical Trials

Today’s clinical trials are faster, have vastly more data, much of it collected directly from the patient via multiple modalities, often outside of traditional investigative sites. Medidata is the only provider that offers a comprehensive decentralized clinical trial (DCT) solution that allows sponsors and CROs to prepare for and analyze high volumes of data at scale. Now, you can move from delayed, reactive methodologies to proactive and predictive strategies that drive better, faster decisions.

Medidata Adjudicate

An effective Clinical Event Committee (CEC) reduces variability in adjudication outcomes, ensuring that the best outcomes are collected in your trial. Having the right endpoint adjudication technology allows you to trace every aspect of the adjudication event, from collection, de-identification and dossier aggregation to committee review and management, giving you control and visibility of all your events.

Medidata Adjudicate is a state-of-the-art clinical endpoint adjudication system, fully integrated with the Medidata Clinical Cloud, providing the unique ability to function as a one-stop shop for all your clinical trial needs. A single solution that follows all clinical events from beginning to final outcome, Medidata Adjudicate is designed to support investigator sites, sponsors, CROs, data managers, and the CEC who collect, manage, organize, adjudicate and submit clinical endpoint data.

Rave CTMS

Simple to Integrate. Simple to Use. Simple to Scale.

A rapidly evolving and complex trial ecosystem has made it more difficult to efficiently manage and oversee clinical trials. Rave CTMS (Clinical Trial Management System) improves speed and efficiency for the oversight of studies, countries, and sites through intelligent automation and workflow management. The Medidata Clinical Cloud™  streamlines the clinical operations ecosystem so data transfer between Rave EDC, Medidata Detect, and Rave eTMF is automated, eliminating manual data re-entry and enabling user-centric workflows that bridge applications.

Rave eTMF

Faster Document Management with a Simple, Automated Trial Master File Solution

Rave eTMF (electronic Trial Master File) is a collaboration platform that streamlines creating, managing, and populating clinical trial content. 

Rave eTMF simplifies clinical document filing by auto-populating TMF content, so that your TMF is always contemporaneous with the trial. Unlike other TMF solutions on the market, Rave eTMF is easily deployed with minimal IT involvement, with an implementation timeline as short as 8 weeks.

Clinical Trial Financial Management

Budget to Payments

Many challenges in clinical trial financial management still exist today and with clinical trials only getting more complex, a solution to address these issues has never been more critical.  Rave Clinical Trial Financial Management (CTFM) provides an end-to-end solution for the financial management of your clinical studies.  

Rave CTFM unifies your study data and financial management in one platform.  Rave CTFM is composed of Rave Design Optimizer, Rave Grants Manager and Rave Site Payments, all paired with the market leading Rave EDC.  

Rave CTFM enables operational efficiencies and financial compliance, collaborative data-driven decision making and greater transparency over planning & execution.

Medidata Risk Management

Quickly Identify Critical-to-Quality (CtQ) Factors and Drive Higher Study Quality

Many risk management approaches rely on siloed spreadsheets, and have not evolved to address the complexities of today’s clinical operations.

Medidata Risk Management provides a dynamic digital solution for risk assessment, monitoring, and mitigation. Now, you can go beyond just being compliant with ICH E6 guidelines, and instead take a proactive approach to manage study risks and ensuring patient safety.

Operationalize your risk management process in a way that spreadsheets simply can’t.