- Promote clinical research according to Good Clinical Practice (ICH-GCP).
- Develop national clinical research network
- Consolidate fundamental and experimental findings by the conduct of clinical research
- Provide access to new and innovative therapeutic approaches through means of a clinical study.
INVESTIGATORS
- Assistance in developing individual clinical research projects
- Submission of research projects to “Comité National d’Ethique de Recherche ”, “Commission Nationale de Protection des Données ” and/or Ministry of Health (* permission to use pending)
- Logistic support for conducting clinical trials including redaction of protocols and case report forms, contracting insurance, elaborating financial conventions, data monitoring and collection, data base set up, statistical analysis, exploitation and publication of results
- Support patient recruitment in trials
- Standard Operating Procedures (SOP): The entire CIEC Team is working according to own CIEC SOP Manual based on ICH – GCP
- Management of patient visits: Individual patient consultations at CIEC (2 fully equipped patient consultation rooms)
- Clinical Trials