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      Accelerate study design, planning, startup and execution for smarter, faster clinical trials.

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      Simplify data workflows with intelligent automation from study build to database lock.

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      The data, tools and insight you need to reimagine clinical trials & propel innovation.

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      Flexible technology to simplify complex study build and execution.

    • Designer

      The central hub for study configuration on the Medidata Platform.

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    • Clinical Data Management & Analytics
      • Data Experience Overview

        Simplify data workflows with intelligent automation from study build to database lock.

      • Adjudicate

        A streamlined, single digital endpoint adjudication system.

      • Clinical Data Studio

        Accelerate clinical data integration, standardization, review, and reconciliation.

      • Coder+

        The evolution in automated medical coding for Rave.

      • Companion

        Make data entry easier and faster for sites.

      • Designer

        The central hub for study configuration on the Medidata Platform.

      • End of Study

        Seamlessly generate, distribute, & manage clinical study files at the end of a study.

      • Imaging

        Gain visibility and full control over your imaging data while simplifying processes.

      • Link

        Combine patient-level clinical trial & real world data.

      • Rave

        Capture and manage your patient, site and lab in the most advanced, robust and secure electronic data capture system.

      • Rave Lite

        A cost-effective offering of Rave for Phase I and Phase IV trials.

      • Remote Source Review

        A cloud-based remote site access and monitoring solution.

      • RTSM

        Eliminate double data entry and change orders for randomization and trial supply management.

      • Safety Gateway

        Automate collection, transmission and tracking of adverse event data.

      • Targeted SDV

        Empowering a risk-based approach to source data verification by focusing on critical data.

    • Patient Engagement
      • Patient Experience Overview

        Ease patient burden and streamline workflows across all trial stages.

      • Decentralized Clinical Trials

        Decentralizing solutions on a unified platform for patients, sites, and sponsors.

      • Digital Therapeutics
      • eCOA

        Full-service, flexible solution to easily and accurately capture patient data and patient reported outcomes.

      • Consent

        A patient-friendly enrollment solution enabling patients to understand trial objectives & consent.

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        A patient portal helping to streamline clinical operations and maintain consistency.

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        Active engagement with Medidata’s diverse patient advocates to infuse the patient voice into solution design.

      • Patient Payments

        Provide patients with a worry-free payment experience.

      • Registries

        Pre- and post-trial engagement to prepare patients for future clinical research participation and enrollment.

      • Sensors

        A complete end to end solution for the normalization and analysis of sensor data and patient information, offering seamless integration to enable rapid decision-making and actionable insights.

    • Clinical Trial Design & Management
      • Study Experience Overview

        Accelerate study design, planning, startup and execution for smarter, faster clinical trials.

      • CTMS

        Improve speed and efficiency for the oversight of studies with Medidata CTMS (Clinical Trial Management System).

      • Diversity in Clinical Trials

        A multi-faceted approach to cultivate diversity across the clinical trial lifecycle.

      • eTMF

        Manage electronic trial master file content while maintaining readiness & compliance.

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      • Grants Manager

        Quickly and accurately develop investigator grant budgets.

      • Integrated Evidence

        Connecting historical insights & real-world data to increase trial success probability.

      • Intelligent Trials

        Operational analytics built on the industry’s largest real-time performance dataset.

      • Protocol Optimization

        Design smarter, more efficient trials using AI.

      • Site Payments

        Unify your clinical research study data and financial management in one platform.

      • Synthetic Control Arm (SCA)

        A smarter external control arm built with regulatory-grade, historical clinical trial data.

    • Healthcare & Therapeutic Solutions

      Designed to tackle the complexities of oncology and vaccine clinical trials safely and cost-effectively.

      • Health Record Connect

        Securely and compliantly exchange EHR and other healthcare data to power a whole new level of collaboration and patient care.

      • Surgical Planning

        Collaborate in real-time for implantable device procedures.

      • Therapeutic Area Solutions

        Designed to tackle the complexities of oncology and vaccine clinical trials safely and cost-effectively.

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        Simplify, future proof, and save time and costs for your clinical study build.

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Study Experience Overview
  • Clinical Trial Financial Management Data-powered financial management
  • CTMS Clinical trial management system
  • eTMF Electronic trial master file
  • Grants Manager Site budgeting
  • Protocol Optimization Smarter study design
  • Site Payments Global payment solution
  • Study Feasibility Clinical trial analytics
  • Synthetic Control Arm ® Smart external control arm
  • Why Experiences
Patient Experience Overview
  • eCOA Electronic clinical outcome assessments
  • Consent Enrollment for clinical trials
  • Decentralized Clinical Trials Flexible, hybrid trials
  • Medidata Diversity Program Trial diversity solutions
  • myMedidata Patient portal
  • myMedidata Registries Pre- and post-trial patient engagement
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  • Sensors Digital measures
  • Why Experiences
Data Experience Overview
  • Adjudicate Endpoint adjudication
  • Clinical Data Studio Data quality management
  • Coder+ Automated medical coding
  • Companion eSource/EHR-to-EDC
  • Designer Central study build hub
  • Health Record Connect Healthcare data interoperability
  • Imaging Medical imaging management
  • Link Trial data linkage to real-world data
  • Rave Electronic data capture
  • Rave Lite EDC for Phase I, IV, and MedTech
  • RTSM Randomization and trial supply management
  • Safety Gateway Automated safety case transmission
  • Site Cloud: End of Study End of study site file archiving
  • Surgical Planning Collaborative surgical planning
  • Targeted SDV Risk-based source data verification
  • Why Experiences
Professional Services Overview
  • Customer Success
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  • Why Experiences
  • Clinical Trial Financial Management Data-powered financial management
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  • Integrated Evidence Real-world data insights
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  • Study Feasibility Clinical trial analytics
  • Patient Insights Program Data-driven insights into participation barriers
  • Site Insights Program Real-world feedback, built in
  • Synthetic Control Arm ® Smart external control arm
  • Consent Enrollment for clinical trials
  • Designer Central study build hub
  • Protocol Optimization Smarter study design
  • Study Feasibility Clinical trial analytics
  • Adjudicate Endpoint adjudication
  • Clinical Data Studio Data quality management
  • Coder+ Automated medical coding
  • Companion eSource/EHR-to-EDC
  • CTMS Clinical trial management system
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  • Surgical Planning Collaborative surgical planning
CRO PartnersPartner ProgramFind a PartnerPartner Portal
Emerging & Mid-sized Biopharma Large Biopharma MedTech Academic & Not-for-profit
  • Clinical Data Studio Data quality management
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  • Imaging Medical imaging management
  • Integrated Evidence Real-world data insights
  • myMedidata Registries Pre- and post-trial patient engagement
  • Protocol Optimization Smarter study design
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  • Rave Lite EDC for Phase I, IV, and MedTech
  • Sensors Digital measures
  • Study Feasibility Clinical trial analytics
  • Surgical Planning Collaborative surgical planning
  • Synthetic Control Arm ® Smart external control arm
  • Targeted SDV Risk-based source data verification
  • Companion eSource/EHR-to-EDC
  • CTMS Clinical trial management system
  • Decentralized Clinical Trials Flexible, hybrid trials
  • eCOA Electronic clinical outcome assessments
  • Medidata Diversity Program Trial diversity solutions
  • myMedidata Patient portal
  • Patient Insights Program Data-driven insights into participation barriers
  • RTSM Randomization and trial supply management
  • Site Insights Program Real-world feedback, built in
  • Clinical Data Studio Data quality management
  • Companion eSource/EHR-to-EDC
  • Decentralized Clinical Trials Flexible, hybrid trials
  • Imaging Medical imaging management
  • Link Trial data linkage to real-world data
  • Sensors Digital measures
  • Clinical Trial Financial Management Data-powered financial management
  • Grants Manager Site budgeting
  • Patient Payments Payment and reimbursement
  • RTSM Randomization and trial supply management
  • Site Payments Global payment solution
  • Adjudicate Endpoint adjudication
  • Consent Enrollment for clinical trials
  • eTMF Electronic trial master file
  • Imaging Medical imaging management
  • Integrated Evidence Real-world data insights
  • myMedidata Registries Pre- and post-trial patient engagement
  • Patient Insights Program Data-driven insights into participation barriers
  • Protocol Optimization Smarter study design
  • Safety Gateway Automated safety case transmission
  • Site Cloud: End of Study End of study site file archiving
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