DATA EXPERIENCE

The Medidata Data Experience connects every part of the clinical data process. From study build to data capture, database lock, and regulatory submission, it leverages built-in AI and automation to simplify workflows, reduce manual effort, improve data quality, and shorten trial timelines—turning raw data into real insights faster.

• Precise, Consistent, Faster Medical Coding For Clinical Trials

  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.

• Rave TSDV - Improve CRA Efficiency And Reduce Site Burden

  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.

• Medidata RBQM – Your Path To Clinical Operations Excellence

  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.

• Optimize Your Endpoint Adjudication On A Single Platform

  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.

• Clinical Data Studio: Unlock The True Power Of Clinical Trial Data

  Experience a transformative AI-powered data quality management solution that unifies study teams by providing seamless access to data from all clinical data sources.

PATIENT EXPERIENCE

The Medidata Patient Experience provides an end-to-end technology solution throughout the entire clinical trial journey. From patient recruitment to in-trial activities and study completion, Medidata provides a full suite of capabilities, all centralized on a single unified platform. This approach simplifies the experience for patients while optimizing workflows for sites.

• Improving The eCOA Experience

  Discover how template-driven builds and reuse can slash eCOA timelines by 50% while solving the licensing and translation hurdles that delay First Patient In.

• Medidata Patient Insights Program

  Learn how Medidata is offering sponsors and CROs access to the award winning Patient Centricity by Design process to help guide the creation of protocols and patient-facing solutions to improve clinical trial experiences.

• CNS Trials With Sensors To Capture Patient Data

  Learn how sensor data and digital endpoints can address challenges in central nervous system (CNS) clinical trials.

• Learning About The Sensors In myMedidata

  Learn how sensor data and advanced analytics can transform clinical research and enable your study to overcome data challenges, improving patient care.

• Protect Personally Identifiable Information (PII) With My Medidata

  Medidata is empowering patients to access their information indefinitely, gain control of their own data security, and leverage Patient Cloud services for their clinical study.

STUDY EXPERIENCE

The Medidata Study Experience accelerates clinical trial design and management by seamlessly connecting workflows, data, and teams. Powered by AI and advanced analytics, it enables sponsors to simulate and optimize trial designs before committing resources. It streamlines critical activities like protocol design, site feasibility, budgeting, and execution, and delivers actionable insights that reduce risk, improve decision-making, eliminate redundancies, and keep operations on track

• Automated Trial Monitoring Workflows Make A Lean Team More Efficient

  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.

• Drive Efficiencies And Speed With Secure, Remote Monitoring

  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.

• Intelligent Clinical Trials: Enhance Study Design And Live Forecasting

  The integration of standardized, regulatory-grade clinical trial data has become central to advancing trial design and execution.

• Medidata CTMS - On Time. On Budget. In Sync

  Learn how you can build support for both sponsor-led and CRO-managed trials with seamless execution, transparency, and control.

• Synthetic Control Arm®: The Smart External Control Arm Solution

  Discover how an external control arm can help you generate rigorous evidence, accelerate decisions, and keep your trial on track when a concurrent control isn’t feasible.

OTHER

• 5 Quick Tips To Accelerate Your Study Build

  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.

• The Next-Generation Of Clinical Trial Data Management And Operations

  This platform benefits sponsors seeking faster study cycles and regulatory compliance, CROs, MedTech companies, and research sites globally.

• Challenges And New Approaches To Developing Clinical Evidence For Medical Devices

  Learn about the challenges and new approaches to developing clinical evidence for medical devices, including decentralized trials, adaptive studies, in silico trials, and real-world evidence.

• Powering Smarter Treatments And Healthier People

  Explore Medidata's commitment to transforming the life sciences sector, fostering patient-centric trials, and creating new opportunities for healthier populations globally​​.

• Powering Smarter Treatments And Healthier People

  Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes.