Clinical studies in hospitals or in private practices.
- Our services
- Protocol design.
- Ethic Committee (CPP) filings.
- Development of CRFs, investigator's brochure, etc.
- Study implementation and monitoring.
- Clinical data mangement and statistical analysis.
- Data Management
- Clinical trial data set-up, monitoring, validation and freezing
- Biostatistics
- Data analysis
- Minimum population calculations
- Randomization
- Development of experimental plans of actions
- Validation of designs of experience
- Preparation of study reports according to GCP-ICH.
- We also offer...
- To provide our own Clinical Research Assistant (CRA) personnel to monitor studies.
