Beerse, Belgium

28th November 2017

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Registrations per company are limited to 20% of maximum attendance.

 

Theme:

Bringing Value to Patients: A Data-quality Perspective

 

Description:

Clinical research is about generating information to support decision-making while guarding subject safety and ethical treatment. The data should be sufficient quality to support good decision-making to maximise the potential impact of research for patients and the public. Advancements and innovations in early data access, efficient data quality control and risk-based quality management are crucial in assuring reliability of trial results and, ultimately, the wellbeing and safety of trial subjects.


This event aims to bring together inspiring speakers and leading industry experts in the field of data management, risk-based monitoring and other relevant areas, to share knowledge and best practices and discuss future developments.

 

Location:

Janssen R&D

Beerse, Belgium

 

Agenda:

TimePresentationsPresenter
8.30 - 9.00am Registration  
9.00 - 9.15am Introduction Kris Lauwers,
Janssen R&D (SDE Co-Chair)
9.15 - 10.00am Analytical Risk-based Monitoring at Janssen Marion Wolfs & Sina Djali,
Janssen R&D
10.00 - 10.30am PhUSE Update Stephen Bamford,
PhUSE Global Events Director
10.30 - 11.00am Managing Quality Registry Data for Effective Exploration: A Quality Perspective Peter Tormay,
Capish
11.00 - 11.15am Morning Break  
11.15am - 12.00pm Interactive Dashboards for Early Data Access and Data Quality Control in a Clinical Trial Femke Sijtsma & Lieke Gijsbers,
OCS Life Sciences
12.00 - 12.30pm Democratising Visual Analytics in Clinical Development Christof Gänzler & Mark Demesmaeker,
PerkinElmer
12.30 - 1.30pm Lunch  
1.30 - 2.15pm A Risk-based Approach to Data Management Andrew Taylor,
GCE Solutions
2.15 - 2.45pm Monitoring Data and Information Quality in Clinical Studies Bernd Heinen,
SAS
2.45 - 3.15pm Towards Better Data Johannes Ulander,
S-CUBED
3.15 - 3.30pm Afternoon Break  
3.30 - 4.00pm Tools and Processes for Data-driven Monitoring and a Risk-based Approach Giulia Zardi & Marika Zanin,
CROS NT
4.00 - 4.30pm The Art of Defensive Programming - Coping with Unseen Data Philip Holland,
Holland Numerics
4.30 - 5.00pm The Role of Programmers in Flawless Execution of RBM Trials Jill Ophoff,
Janssen R&D
5.00 - 5.30pm A Holistic View on Clinical Data Quality Pieter Stas,
Business & Decision Life Sciences
5.30 - 5.45pm Closing remarks  

Catering and refreshments will be provided throughout the day.

 

SDE Chairs:

Heidi Curinckx, Janssen R&D

Kris Lauwers, Janssen R&D

If you have any questions, or require any information, please contact the SDE Co-Chair.

 

Sponsors:

If you are interested in sponsoring this event, click here.

        

Hotels:

To follow.

 

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