Trial Management

  • How to Select Most Effective eCOA Modality for Your Study1:02:21

    How to Select Most Effective eCOA Modality for Your Study

    This webinar examines the electronic Clinical Outcome Assessment (eCOA) modalities available to clinical trials, such as handheld, tablet, web, Bring Your Own Device (BYOD), and mixed mode devices.

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  • Managing eCOA Data - Principles and Best Practices

    Managing eCOA Data - Principles and Best Practices

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  • 9 KPI Dashboards & Reports No eCOA Study Should Be Without

    9 KPI Dashboards & Reports No eCOA Study Should Be Without

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  • How to Visualize Data to Increase Trial Performance and Efficiencies48:54

    How to Visualize Data to Increase Trial Performance and Efficiencies

    This live demo shows how new visualization tools in CRF Health’s TrialManager 6.0 enable monitoring of patients and sites in real time, resulting in lower clinical trial costs and higher data quality.

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  • SCDM Presents: Managing eCOA Data - Principles and Best Practices1:04:19

    SCDM Presents: Managing eCOA Data - Principles and Best Practices

    At the invitation of SCDM, CRF Health reveals common issues related to data management. Presenters draw on real-life eCOA clinical studies to outline best practices for achieving high data quality.

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  • Developing an eCOA Device Supply Strategy: The Vital Considerations for a Global Clinical Trial

    Developing an eCOA Device Supply Strategy: The Vital Considerations for a Global Clinical Trial

    With the increasing complexities of today's clinical trials, including the ever-rising number of studies spanning numerous continents and sites, managing the cost of a global trial can prove challen

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  • What Metadata Can Teach Us About Actual Patient Reporting Behavior46:59

    What Metadata Can Teach Us About Actual Patient Reporting Behavior

    Anders Mortin of TriTiCon presents research findings on patient compliance in long-term clinical trials. Learn how eCOA metadata can help you identify patient reporting behaviours and preferences.

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  • The Shocking Truth About Paper Backups in eCOA Studies57:32

    The Shocking Truth About Paper Backups in eCOA Studies

    While paper has long been the trusted system for clinical trial backup, a recent study reveals the medium does carry risk. Learn how eCOA can mitigate risk and relieve the burden of managing paper.

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  • The Challenges of Paper Backups in eCOA Studies

    The Challenges of Paper Backups in eCOA Studies

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  • Effective ePRO Training Increases Patient Compliance

    Effective ePRO Training Increases Patient Compliance

    Brought to your by CRF Health and the TrialMax eCOA Solution - visit www.crfhealth.com for more information

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  • Managing eCOA Device Allocation and Resupply in Clinical Trials

    Managing eCOA Device Allocation and Resupply in Clinical Trials

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  • PROs and Your Clinical Trial: Choosing, Administering, and Claiming1:01:02

    PROs and Your Clinical Trial: Choosing, Administering, and Claiming

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  • Measuring Patient ePRO Burden Through Completion Times56:12

    Measuring Patient ePRO Burden Through Completion Times

    Rob Arbuckle, Chloe Tolley, and Karl McEvoy present research findings related to diary completion times in clinical trials, suggesting best practices for reducing patient burden with ePRO solutions.

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  • Integrating Today's eCOA Solutions Intelligently and Efficiently44:58

    Integrating Today's eCOA Solutions Intelligently and Efficiently

    Keith Wenzel and Rauha Tulkki-Wilke draw on case studies to give review the current electronic data gathering environment and identify best practices for eCOA integration into clinical studies.

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  • Overcoming Logistical Challenges in Global Clinical Trials42:33

    Overcoming Logistical Challenges in Global Clinical Trials

    Deploying eCOA in a global clinical study requires a reliable supply chain, as well as an understanding of trade protocols for individual countries as they relate to importation of electronic devices.

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  • Successful Management of eCOA Data22:47

    Successful Management of eCOA Data

    Chapter 2 of a two-part series, providing an overview of electronic data collection. Nora Ibrahimova covers best practices for implementation of eCOA and management of real-time assessment data.

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  • Clinical Outcome Assessments and Your Study41:16

    Clinical Outcome Assessments and Your Study

    Andrea Murison of Mapi Research Trust joins Paul O’Donohoe to discuss considerations and resources for selecting clinical outcome assessments for a clinical trial and discuss adaptation to electronic.

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  • Which ePRO Solution is Right for your Study? (I)40:22

    Which ePRO Solution is Right for your Study? (I)

    Part 2 of 2: Robyn Carson, Elsie Mathews, and John Jordan discuss various types of ePRO and outline considerations for selecting an appropriate mode for a clinical study. Recorded January 20, 2011.

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  • For CROs: ePRO Best Practices - Part I49:14

    For CROs: ePRO Best Practices - Part I

    Part 1 of 2: Gregg Jewett discusses the state of the clinical trials industry, outlining benefits and best practices for CROS and sponsors within a CRO-ePRO partnership. Recorded March 17, 2011.

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  • For CROs: ePRO Best Practices - Part II59:45

    For CROs: ePRO Best Practices - Part II

    Part 2 of 2: An overview of benefits and best practices for CRO-ePRO partnerships with particular focus on business development, operations and delivery, and data management. Recorded April 21, 2011.

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