The protocol is the most important document of a clinical research project and the key of the success of your research project.
This course will teach you how to write a protocol and will give you all the basic elements according to good Clinical Practice to write a protocol in the respect of ethical rules and participant protection.
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.
SAVE THE DATE 28th May 2016 10am - 4pm
VENUE Centre Hospitalier Luxembourg (CHL) Amphithéâtre 4, rue Barblé L-1210 Luxembourg
AGENDA The agenda will be sent to you very soon and be available on our website.
INFORMATION & REGISTRATION tania.zamboni@lih.lu
As the number of seats is limited, we will accept registrations on a first come first served basis.
IN COLLABORATION WITH
for articles/videos/studies
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.