One of the main objectives of the Clinical and Epidemiological Investigation Center in Luxembourg (CIEC) is to promote clinical research activities according to international standards of good clinical practice.
This year again, the CIEC has partnered up with CHL in order to organize a half-day interactive and certified training in “Good Clinical Practice” focusing on risk-based monitoring in clinical research.
The monitoring is an important activity that ensures the quality of the collected data. The principal investigator is the main responsible of these data. This course will teach you a new monitoring approach.
Unlike standard monitoring which aims to verify 100% of data, risk-based monitoring (RBM) intends to reduce and optimize monitoring activities.
After successful completion of a test at the end of the training, the participants will obtain a certificate that will document their knowledge of GCP.
As the number of seats is limited, we will accept registrations on a first come first served basis.
Save the date now: 10th June 2015 from 13h30 – 17h30.
The agenda will be sent to you very soon and be available on our website www.luxclin.lu.
Course venue: Centre Hospitalier Luxembourg (CHL) – Amphithéâtre - 4, rue Barblé L-1210 Luxembourg-Strassen
Information and registration: tania.zamboni@lih.lu
Registration fees: 60€ per participant to be paid before the training: contact Tania Zamboni by responding to this e-mail.
More information here: www.luxclin.lu/Events/Details/?c=EVT5228BDN
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Healthcare professionals who wish to be part of a unique network, providing access to up-to-date, accurate and validated information about clinical research.
Investigators and study staff who wish to be part of a unique network, in order to stay abreast of clinical trials taking place in Luxembourg and who are willing to further develop their competencies.
