Monitoring

Monitoring is responsible for quality control, for supervision of the progress of the clinical trial and for ensuring that the latter is carried out and documented in compliance with the protocol, standard operation procedures (SOP), good clinical practice as well as the applicable statutory provisions.

As part of the preparation for each clinical trial the responsibilities to be assumed by the monitor in such a trial is defined in the monitor’s manual. CenTrial assumes the entire monitoring of clinical trials by its own employees, or works together with your monitoring team as part of it.