On-site clinical studies.
- Our services
- Protocol design.
- Ethic Committee (CPP) filings.
- Development of CRFs, investigator's brochure, etc.
- Subject recruitment.
- Study implementation and monitoring.
- By our CRAs .
- With assistance provided to sponsor Clinical Research Assistants (CRAs) by our own CRAs.
- Clinical data management 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...
- Bio-equivalence studies on generics.
- Minor surgical procedures.
- Use of healing models (biopsies, suction blisters, etc.).
- Creation of inflammation models (actinic, chemical, etc.).
- Proof of concept studies.
- Objectivation of effects observed via biometrological measurements.
- Photobiology: phototoxicity and photosensitization tests.
- Illustration of obtained results with standardized photographs
- etc
