RCTS : études cliniques

• Elaborate and print out a perfectly operational CRF,
• Discuss with you the organisation of study drug supplies,
• Select and recruit investigators either from our or your database,
• Present the study to the investigators through setting-up meetings or individual visits,
• Meet the pharmacists and the hospital directors,
• Conceive and produce the study kits provided with all the study material,
• Adapt our general procedures to the specificity of the study,
• Meet with you regularly to better co-ordinate our actions.

Our teams of site CRAs and central CRAs master all the logistics of clinical trials. They apply widely tested procedures and use advanced logistic tools.

Under the supervision of a dedicated Project Manager, they can manage all logistical aspects of the study in the shortest possible time and use the highest quality standards during this key phase of the study.