Services in Clinical Studies - organizacja i nadzór badań klinicznych mgr Olga Pokorska

Services in Clinical Studies provides: + Project management support + Support in locating and assessing the suitability of facilities at a study centre + Support in briefing doctors/consultants on conducting the trial + Setting up the study centres (includes submission to CA and/or EC), ensuring each centre has the trial materials and training site staff to trial specific and industry standards + Monitoring the trial through its duration + Verifying that data entered on to the CRFs is consistent with patient clinical notes (source data/document verification SDV) also in the eCRF + Collecting completed CRFs + Writing visit reports + Filing and collecting trial documentation and reports + Drug accountability + Closing down study centres on completion of the trial + Archiving study documentation and correspondence + CRA Academy - courses and training