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Monitoring
Monitoring
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.
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