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  • 3 Ways Electronic Informed Consent Benefits Trial Participants3:59

    3 Ways Electronic Informed Consent Benefits Trial Participants

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  • Webinar: How to Calculate the True Cost of Paper When Considering eCOA

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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

    <p>Identifying hidden patterns in patient behavior can help you run an efficient and successful clinical trial. With powerful new visualization tools for reporting and analysis, CRF Health's TrialMan

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  • Understanding the EMA Oncology PRO Guideline Appendix – We Can Help!

    Understanding the EMA Oncology PRO Guideline Appendix – We Can Help!

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  • How to Select the Most Effective Modality for My eCOA Study

    How to Select the Most Effective Modality for My eCOA Study

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  • eCOA, Patient Centricity and the Path to More Accurate Data3:41

    eCOA, Patient Centricity and the Path to More Accurate Data

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  • What the Future Holds for Informed Consent

    What the Future Holds for Informed Consent

    Mika Lindroos, Director of Product Management at CRF Health, discusses the advantages of electronic informed consent in clinical trials and how by integrating this process with eCOA technologies, rese

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  • The Data Point's Perspective on Clinical Outcome Assessments 2:05

    The Data Point's Perspective on Clinical Outcome Assessments

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  • eCOA Impact on Data Quality 3:28

    eCOA Impact on Data Quality

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  • BYOD: One Instrument Developer's Technical Solution28:29

    BYOD: One Instrument Developer's Technical Solution

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  • The Integration of Patient Portals & eCOA Systems30:02

    The Integration of Patient Portals & eCOA Systems

    <p>Patient centricity is ever growing. The field has expanded the involvement of patients and their voice into planning, execution, and even the purpose of clinical and medical research. The next evol

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  • eCOA in Global Studies: Considerations and Best Practices for Localization21:38

    eCOA in Global Studies: Considerations and Best Practices for Localization

    <p>Utilizing eCOA for data collection with non-English speaking patients requires planning for translating the content on the devices, as well as providing related services like rater training and hel

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  • Patient-Centered Outcomes in 2016: What's New, and What's Not Likely to Change35:57

    Patient-Centered Outcomes in 2016: What's New, and What's Not Likely to Change

    <p>The landscape of Patient-Reported Outcomes measurement is changing. Learn more about the Mapi interpretation about facts, events, and trends. Get a top-level understanding of the Patient-Centered O

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  • A Review of FDA PRO Labeling (2011-2015)32:54

    A Review of FDA PRO Labeling (2011-2015)

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  • Mixed Mode Data Collection: Minimizing Risk and Managing Data31:50

    Mixed Mode Data Collection: Minimizing Risk and Managing Data

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  • Body Maps: User Perspectives on Reporting Symptom Location21:50

    Body Maps: User Perspectives on Reporting Symptom Location

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  • Researcher Discretion in Determining Equivalence Across Modes in COA Instruments39:26

    Researcher Discretion in Determining Equivalence Across Modes in COA Instruments

    <p>Learn more about the crucial decisions in the design and analysis of mode equivalence studies and how these decisions can affect study conclusions. Decisions include study design (basic design, tar

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  • The Social Patient: How Social Media is Helping Sponsors Partner with Patients to Design Better Clinical Trials23:39

    The Social Patient: How Social Media is Helping Sponsors Partner with Patients to Design Better Clinical Trials

    <p>Clinical trials shouldn’t be burdensome for patients. Keep it simple by partnering with patients to ensure trials are designed with their needs in mind. Also covered: the effectiveness of PatientsL

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

    SCDM Presents: Managing eCOA Data - Principles and Best Practices

    <p>In this webinar, SCDM invites CRF Health to discuss the principles of managing eCOA data in clinical trials. We will use experience from real life studies to illustrate how to handle issues clinica

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  • Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension1:00:01

    Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension

    <p>Informed consent has a major impact on regulatory compliance, enrollment rates and expenses across the life of your study. Yet the traditional paper-based process has transformed informed consent i

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  • eCOA vs Paper: Head-to-Head

    eCOA vs Paper: Head-to-Head

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