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.

• Imaging Services: One Place For Your Imaging Management

  Medidata is revolutionizing clinical trial imaging management. This cutting-edge cloud-based solution combines advanced technology with expert Core Lab support for quality control activities.

• Manage Exponential Data Growth With Medidata Clinical Data Studio

  Bring study teams together like never before for total data quality oversight.

• Clinical Data Studio: A Single Data Review Platform Fostering Unification Across Groups

  This end-to-end digital review platform can assist both your risk management team and data management team, improving speed and facilitating database lock times.

• Integrating Clinical Trial Data For Comprehensive Data Quality Oversight

  As clinical trials increasingly rely on diverse, complex data streams, a solution for data integration and quality assurance becomes critical to overcome these challenges.

• Bridging The Gap Between EHR And EDC

  Clinical trial sites have long relied on manual, error-prone processes to transfer patient data from EHRs into EDC systems, but integrated solutions make streamlining this workflow quick and simple.

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.

• At The Crossroads Of Data: eCOA And Sensors Converging For Novel Insights

  Leveraging sensors and eCOA addresses increasing clinical trial complexity and ensures a more efficient and effective study design.

• Aligning Site And Patient Needs For Clinical Trial Success

  Redefine clinical trial execution by aligning site and patient needs through a unified, intelligent platform.

• Streamline Payments On The Most Widely Adopted Clinical Data Platform

  Allow patients to choose their preferred payment method, ensuring convenience and control while supporting efficient clinical trial operations.

• Usability Is Data Quality

  With sponsors are better equipped to generate reliable CNS outcomes and advance therapies with confidence.

• Double Down On CNS Endpoint Data Quality

  Central nervous system (CNS) clinical trials demand exceptional data quality, and streamlined, unified EDC and monitoring systems are setting a new standard for operational excellence and data integrity in CNS trials.

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

• Achieve Financial Management Success With Rave CTFM

  Achieve operational and resource planning success for your clinical trial with the help of Rave Clinical Trial Financial Management (CTFM).

• Medidata CTMS Leads The Industry

  The 2024 Everest Group PEAK Matrix assessment has named Medidata CTMS the leading Clinical Trial Management System (CTMS).

• Accelerate Your Operations With Smarter Trial Management

  Learn about a cloud-based solution that centralizes clinical and operational data to improve the efficiency and oversight of clinical trials.

• Intelligent Trials: Design and Execute Faster Trials with AI-Powered Insights

  Explore how Intelligent Trials leverages the industry’s largest clinical dataset to accelerate enrollment, improve diversity, and provide real-time insights, ensuring efficient, data-driven trial success.

• FDA Draft Guidance On Diversity Action Plan Requirements

  Explore new drafted guidance under FDORA that substantiates the mandate of a Diversity Action Plan (DAP) for late-stage trial protocol submissions.

OTHER

• 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.

• Five Quick Tips To Accelerate Your Study Build

  This eBook outlines five specific tips that can be applied to accelerate and optimize your study builds today, and into the future.