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Welcome to the European Forum for Good Clinical Practice
Activities  >  Events and Activities  >  Clinical Study Reporting – Effects of the Coronavirus Pandemic
Webinar
Clinical Study Reporting – Effects of the Coronavirus Pandemic
Quality and ethics experts respond to your questions from sponsor and site points of view.
15 June 2020 -- 17:00-18:00 CESTAdd to calendar
Description
Description

Our Free of Charge weekly Q&A Webinars on Clinical Trials During the Corona Virus Pandemic are continuing!
Quality and ethics experts respond to your questions from sponsor and site points of view.

Ask your Questions Upfront and get more information during the Webinar: Click Here

    Clinical Study Reporting – Effects of the Pandemic
    Moderator: Mark Poulton, Poulton Quality Solutions

    Presenters:
  • Regulatory Guidelines laid down for CSRs: Louise Mawer, Mirabilitas & Seif Eddine Amara Madi, GSK
  • Statistical Aspects of Reporting and Data Integrity Issues: Nancy Carpenter, Veramed

  • Panellists:
  • Cathy Dove, Dove Quality Solutions
  • Beat Widler, WS QMS
  • Matt Jones, Digital Quality Associates
  • Heather Sampson, University of Toronto
  • Hugh Davies, Oxford A Research Ethics Committee
  • Sarah Hall, Mipsol Limited
  • Claire Khalil, Evlo Biosciences
  • Sylvia Kranich, SK Consulting
  • Michelle Gabriel, University College London


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EFGCP
European Forum for Good Clinical Practice
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