ONE DAY INTRODUCTION TO EORTC TRIALS 2008

This course is dedicated to newly participating members (investigators, data managers, research nurses, etc.), and industry representatives. The purpose of this introductory workshop 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 course: ONE-DAY INTRODUCTION TO EORTC TRIALS
Flyer in pdf version Course Homepage Program Course Registration Form Hotel Reservation Cancellation policy Education Office Program 2008	2 October 2008 (*) 3 October 2008 () EORTC Headquarters 83 avenue E. Mounier, 1200 Brussels, Belgium
	WARNING () Please be informed that registration for the course of Friday 3 October is now closed as we have reached the maximum number of participants for this course. () We would like to propose you to attend an identical course organized on Thursday 2 October. Please kindly note that registrations received after 28 August 2008, will be confirmed for the course of 2 October* 2008 only. Thank you for your understanding.
	General information
	*Chairperson*
	Ann Marinus, Head Operations Department, EORTC Headquarters
	*Who should attend?*
	Anyone who is new to the clinical research area or has recently started working with EORTC protocols.
	*Workshop description*
	This course is dedicated to newly participating members (investigators, data managers, research nurses, etc.), and industry representatives. The purpose of this introductory workshop 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 Activities - Study development at EORTC - Trial methodology: introduction - Investigator responsibilities, how to be ready for audit & inspection - Patient safety: reporting of Adverse Events and Serious Adverse Events - Reliable data through adequate CRF (Case Report Forms) development, completion and review - Randomization & Remote Data Capture at EORTC.
	*PLEASE REGISTER BEFORE 15 SEPTEMBER 2008*

	EORTC AISBL / IVZW Avenue Mounierlaan, 83/11 Brussel 1200 Bruxelles • Belgie Belgique +32 2 774 16 11
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