Clinical Operations Solutions
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5 Quick Tips To Accelerate Your Study Build
1/7/2026
Here, we outline five practical, actionable tips to help study build teams accelerate timelines while maintaining quality — delivering immediate impact today and sustainable benefits well into the future.
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Automated Trial Monitoring Workflows Make A Lean Team More Efficient
1/7/2026
A pharmaceutical therapy developer was looking to automate reports, confirmation letters, and follow-up letters. See what happened when they adopted a cloud-based solution for end-to-end trial management.
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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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Drive Efficiencies And Speed With Secure, Remote Monitoring
1/5/2026
Medidata Remote Source Review is a cloud-based solution that rapidly and remotely enables monitors to acquire critical documents, automates document workflows to the right monitor for the right study and site and allows him/her to review documents to support SDV and SDR. This allows for real-time assessment of subject safety and data quality compared to traditional onsite monitoring efforts.
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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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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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Accelerate Your Operations With Smarter Trial Management
1/22/2025
Learn about a cloud-based solution that centralizes clinical and operational data to improve the efficiency and oversight of clinical trials.