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Artialis will ensure training and initiation of sites at the trial start by in-house clinical project leaders and clinical research associates.
Monitoring will be done by a specialized CRA in our therapeutic field. Monitoring includes site-monitoring and remote monitoring activities. These activities include also site regular contacts and close follow-up during the trial, queries, and deviation management. After database lock, Artialis will ensure the closure of sites.
Investigators network & experts
eTMF solutions & documentation
Clinical Data Management
Product vigilance & safety
Type of studies
11, Avenue de l'Hôpital
Tour GIGA +3
4000 Liège (Sart-Tilman), Belgium
Business Registration Number: 0830584472
Tel. +32 4 242 77 27
Fax +32 4 242 77 28
For any question, request or order of ELISA kits, please contact our customer service at
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