ECCI - European Consortium of Clinical Investigators

Benefits
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Advantages of co-operation with ECCI for clinical trial sponsors

Access to pre-approved quality investigative sites with trained experienced investigators and a proven capacity for fast and large-scale patient recruitment in all main therapeutic areas. 

Selection of most appropriate principal investigators and facilitated access to opinion leaders in all countries where ECCI operates.

All ECCI sites subscribe to standard SOPs ensuring quality of clinical conduct and strict adherence to GCP

Central communication through ECCI will streamline the management process of multi-centre trials and help to avoid language and other problems in interaction between the sponsor and the investigative sites.

Regulatory expertise available within ECCI will guarantee smooth and effective co-operation with national regulatory and ethical authorities.

On sponsor's request, ECCI can strengthen investigative sites with its own personnel - experienced clinical trial co-ordinators - to ensure successful implementation of clinical trials of any size and complexity.