Contact Person
    Nicole Mastrell

    Event Manager & PA to CEO
    Email: nm@mva.org
    Phone: (M) +45 6141 8634 Linkedin

    Establishing clinical trial safety and efficacy – Boost Seminar

    We are pleased to invite you to a half-day seminar where you will learn how to facilitate trial safety and efficacy with automated reporting tools, roll-based workflows and clinical analysis capabilities including risk-based monitoring, data monitoring and fraud detection.

    Date: Tuesday May 23rd, 2017
    Time: 10:00 – 13:30
    Venue: Medicon Village, Scheelevägen 2, 223 63 Lund, Sweden – Auditorium

    The seminar is FREE, but please make sure to register:

    SIGN UP

    Medical writers and clinical data scientists will learn how to:

    • Automate significant portions of the clinical study reporting process, reducing the time and complexity underlying adverse event narrative submission.
    • Build summary dashboards to help evaluate safety and efficacy issues in a single click.
    • Generate customised patient narratives and patient profiles.

    Data managers and clinical operators will learn how to:

    • Minimise data quality risks with risk-based monitoring tools in JMP Clinical that make it easy to identify outliers and data anomalies at any level of the organisation.
    • Isolate factors responsible for data integrity issues.
    • Ensure data quality with visualisations that make it easy to identify modified or duplicate data.

    PROGRAM

    10:00

    Registration and Coffee

    10:30

    Introduction

    10:40

    Learn how Clinical Data Scientists support trial safety and efficacy data for validity, monitoring and submission
    purposes. They often overlap and support both medical monitors and medical writers as well as others throughout
    ongoing trials.
    By Valérie Nedbal

    11:20

    Break

    11:50

    Learn how Data Management and Clinical Operations work together using visualization and algorithms in ongoing
    data cleaning efforts as well as an evaluation of how sites and patients are performing on the trial.
    By Richard Zink

    12:30

    Conclusion

    12:40

    Networking Lunch

     
    SPEAKERS 

    Richard C. Zink
    JMP Principal Research Statistician Developer, SAS
    Valerie Nedbal
    JMP Senior System Engineer

     

    IN COLLABORATION WITH

    VENUE SPONSOR:

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