Monitoring is responsible for quality control, for supervision of the progress of the clinical trial and for ensuring that the latter is conducted and documented in compliance with the study protocol, standard operation procedures (SOP), good clinical practice (GCP) as well as the applicable legal provisions.
As part of the preparation for each clinical trial the Monitor`s responsibilities are defined in the monitor’s manual. CenTrial`s Monitors provide the entire monitoring of a clinical trial or become part of your monitoring team.
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