Performances
- Protocol writing
- Project coordination
- CRF development, design, printing
- Investigator recruitment
- Study monitoring
- Electronic CRF experience
- Study secretary / project assistance
- Investigator meetings
- Training of investigators and center personnel
- Study site management (full service)
- Central randomization (also at weekends)
- Data management
- Statistical evaluation
- Biometrical and Clinical Report writing
- Metaanalysis of clinical studies
- Scientific article writing
- All GCP activities
- Quality of Life studies
- Non-Interventional studies (NIS)
- Consulting in all areas of clinical research
- Pharmaco-economic studies (also as add-on to clinical trials)
- Research experience and cooperations in most of European and Scandinavian countries.
