	EORTC AISBL / IVZW Avenue Mounierlaan, 83/11 Brussel 1200 Bruxelles • Belgie Belgique +32 2 774 16 11
EORTC course: ONE-DAY INTRODUCTION TO EORTC TRIALS
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15 October 2010 EORTC Headquarters 83 avenue E. Mounier, 1200 Brussels, Belgium

Ann Marinus, Assistant Director, Project & Budget Development Department, EORTC Headquarters

Who should attend?

Anyone who is new to the clinical research area or has recently started working with EORTC protocols.

Course description

This course is dedicated to newly participating members (investigators, data managers, research nurses, etc.), and industry representatives. The purpose of this introductory course is to give guidance for participating in EORTC clinical trials activities. Participants will receive information about the functioning of the EORTC and about Trials methodology, investigator / site quality requirements and controle, patient safety management, adequate data collection and pitfalls for reliable data. Furthermore you will be shown our on-line registration /randomization process and remote data capture system. It also provides an opportunity to visit the EORTC Headquarters and to have informal discussions with the Headquarters staff.

EORTC Structure and Scientific Strategy - Project development at EORTC - Trial methodology: introduction - Site responsibilities for participation to a clinical trial - Patient safety: reporting of Adverse Events and Serious Adverse Events - Randomization & Data Management systems and processes.

	General information
	*Chairperson*
	Ann Marinus, Assistant Director, Project & Budget Development Department, EORTC Headquarters
	*Who should attend?*
	Anyone who is new to the clinical research area or has recently started working with EORTC protocols.
	*Course description*
	This course is dedicated to newly participating members (investigators, data managers, research nurses, etc.), and industry representatives. The purpose of this introductory course is to give guidance for participating in EORTC clinical trials activities. Participants will receive information about the functioning of the EORTC and about Trials methodology, investigator / site quality requirements and controle, patient safety management, adequate data collection and pitfalls for reliable data. Furthermore you will be shown our on-line registration /randomization process and remote data capture system. It also provides an opportunity to visit the EORTC Headquarters and to have informal discussions with the Headquarters staff.
	*Program*
	EORTC Structure and Scientific Strategy - Project development at EORTC - Trial methodology: introduction - Site responsibilities for participation to a clinical trial - Patient safety: reporting of Adverse Events and Serious Adverse Events - Randomization & Data Management systems and processes.
	PLEASE REGISTER BEFORE 1 SEPTEMBER 2010