Clinical Study Reporting – Effects of the Coronavirus Pandemic

Webinar - Free Q&A Session


Event Webinar
Type Virtual Event
Language English
Date(s) 15 Jun. 2020
Day(s) 17:00 - 18:00
Duration 1 hour

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.


17:00 Introduction to the Webinar
Moderator(s): Mark Poulton, Poulton Quality Solutions
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
Q&A and Discussion
Beat Widler, WS QMS
Cathy Dove, Dove Quality Solutions
Claire Khalil, Evlo Biosciences
Heather Sampson, University of Toronto
Hugh Davies, Oxford A Research Ethics Committee
Matt Jones, Digital Quality Associates
Michelle Gabriel, University College London
Sarah Hall, Mipsol Limited
Sylvia Kranich, SK Consulting
18:00 End of the Webinar