ARCP.be conference

Progam October 2016

08:30-09:00 Registration and Coffee
09:00-09:10 Welcome and Introduction
Yves Geysels, President ACRP.be and
Diane Kleinermans, Advisor to the Minister of Social Affairs and Public Health
Moderator morning session: Josse Thomas, member MEC UZ Leuven and Aly Talen, Genae
09:10-09:35 Latest developments on the European Clinical Trials Regulation
Greet Mush, Director General Pre Authorisation, FAGG
09:35-10:00 Belgium as an attractive country for Clinical Trials in the new Clinical Trials Regulation
Diane Kleinermans, Advisor to the Minister of Social Affairs and Public Health
10:00-10:25 Legal formalities for the establishment of a Database with Health Information
Ann Bracke, Legal Advisor AZ Groeninge
10:25:10:50 Harness healthcare data to accelerate clinical studies and enable world-wide collaborative research
Jack London, Informatics Core Director, Thomas Jefferson University, US
11:00-11:30 Coffee
11:30-12:20 Clinical Research & Development in a globalised world
Ken Getz, Associate Professor and Director CSDD, Founder and Board Chair, CISCRP, US
12:20-12:45 About the value of Patient advocacy Groups and Patient representation
Ysbrand Poortman, co-founder and member of the board of the European Patients Network for Medical Research and Health
12:45-13:00 Celebration: European outstanding Leadership Awards
13:00-14:00 Lunch
Moderator session afternoon: Michèle Garot, BeCRO and Robert Lins, ACRP.be
14:00-14:25 New initatives of Transcelerate
TBC
14:25-15:10 The State of Risk Based Monitoring
Jonas Renström, Associate Director Quintiles, Sweden
15:10-16:00 Panel Discussion on the value of Risk Based Monitoring
Jonas Renström, Associate Director Quintiles, Sweden
Vivienne Van de walle, Prinicipal Investigator PT&R
Michèle Garot, BeCRO
Clara Heering, ICON
16:00-17:00 Master your emails: Towards a new email-culture
Günnar Michielsen