Contact Person
    Nicole Mastrell

    Event Manager & PA to CEO
    Phone: (M) +45 6141 8634 Linkedin

    Industry Seminar: Reducing Your Trial Timelines with Data Analytics

    Are you finding that manual processes are delaying or, even worse, compromising your clinical trial integrity? What if you could reduce the time from LPLV (Last Patient Last Visit) to DBL (Database Lock) cycle time and submit your filing to the NDA sooner? And, as an experienced professional focused on clinical trials, I’m sure you are aware that each additional month of delay can result in millions in lost revenue. 

    The good news is, you can reduce overall trial timelines, while at the same time ensuring that you maintain the highest level of data integrity with the use of analytics.

    At our upcoming session, “Reducing Your Trial Timelines with Data Analytics,” featuring Stella Stergiopoulos, of the Tufts Center for the Study of Drug Development, we will look at how analytics solutions and real world evidence are helping companies like yours reduce timelines, tune trials, and derive insights that help patients. The open forum is designed for personalised discussion where we can all share experiences and best practices.

    This session is free to attend and will include data and analytics experts, industry peers, and thought-leaders.

    To save your spot at the seminar, please click on the registration link below, as we have a limited number of spots available. We look forward to seeing you there.

    For more information, please contact Christy Richardson.


    Dinner Information

    Date: Tuesday 25 April 2017
    Time: 12:00 – 13:00 Networking Lunch
    13:00 – 15:30 Seminar


    Clarion Copenhagen Airport
    Ellehammersvej 20 2770 Kastrup

    Guest Speakers

    Stella Stergiopoulos
    Research Fellow, Tufts Center for the Study of Drug Development


    Sean McDonnell
    Principal Platform Adoption – Data and Analytics, Medidata



    Andrew Gebbie 
    Solution Consultant, Medidata