Clinical Study Reporting – Effects of the Coronavirus Pandemic

Webinar - Free Q&A Session

Description

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.

Programme

17:00 Introduction to the Webinar 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