Medidata, Data Experience
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Precise, Consistent, Faster Medical Coding For Clinical Trials
1/5/2026
Rave Coder provides medical coding for verbatim terms from Rave EDC and external sources using the MedDRA, WHODrug and JDrug dictionaries. Rave Coder centralizes and streamlines medical coding, delivering key benefits to sites, coding specialists and data managers.
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Rave TSDV - Improve CRA Efficiency And Reduce Site Burden
1/5/2026
Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.
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Medidata RBQM – Your Path To Clinical Operations Excellence
1/5/2026
Medidata RBQM (Risk-Based Quality Management) provides the technology and experience to transform your approach to clinical operations towards risk-based study execution models. Now you can continuously monitor data from anywhere, allowing you to innovate and optimize your approach to trial design, physical and virtual interactions with sites, and holistic portfolio strategy.
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Optimize Your Endpoint Adjudication On A Single Platform
1/5/2026
Medidata Adjudicate is part of the Medidata Clinical Cloud™, and offers a cloud-based, end-to-end solution, with easily configurable modules enabling quick setup to manage endpoint adjudication in clinical trials. Medidata Adjudicate supports investigator sites, sponsors, CROs, data managers, and the CEC in collecting, managing, organizing, adjudicating and submitting clinical endpoint data.
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Clinical Data Studio: Unlock The True Power Of Clinical Trial Data
1/5/2026
Experience a transformative AI-powered data quality management solution that unifies study teams by providing seamless access to data from all clinical data sources.
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Managing Risk In Clinical Trials
10/1/2025
Uncover how Risk-Based Quality Management (RBQM) strategies ensure compliance with regulatory guidelines, reduce risks to patient safety, and eliminate inefficient and costly manual processes.
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Unlock The True Power Of Clinical Trial Data
9/8/2025
Explore how the innovative Clinical Data Studio platform can revolutionize your clinical trials by providing complete transparency, harmonized workflows, and superior data integrity.
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Modernizing Clinical Trial Oversight: The Path To Clinical Operations Excellence
8/4/2025
Examine the current state of RBQM approaches to virtualizing clinical oversight, and the value that adopting these approaches brings to sponsors, CROs, sites, and ultimately patients.
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A New Approach To Dynamic Clinical Oversight With Centralized Insights
7/10/2025
RBQM is transforming clinical trial oversight. By automating protocol digitalization, site selection, and risk assessments 360° Monitoring enables the proactive identification of CtQ factors.
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Patient Journey Insights Beyond The Clinical Trial Window
7/10/2025
This patient-level data linkage solution connects clinical trial data (CTD) with RWD, providing a continuous view of a patient’s health journey before, during, and after trial participation.