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This service provides all or part of the management of clinical trial data (Phases I to IV and related phases), from the elaboration of CRF to the integrated report.
The data management and statistical tasks are performed by an experienced team, accustomed to rigorous working practices, and who are capable of integrating quickly and effectively into the project team.
They guarantee a high level of quality and can provide precise and clear documentation at all stages of the process.
- Design of pages according to the Sponsor’s standards
- Proposal of proven standard pages
- Conformity with international standards
- Identification by code-bar
- Printing on self-duplicating paper
- Creation of study files and pack
- Management & shipment of CRFs to Investigation sites