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This service aims to provide management services for all or part of the clinical trial (Phases I to IV and related phases), from the protocol design to the integrated study report.
The mission is entrusted to experienced collaborators, accustomed to rigorous working practices, and who are capable of integrating quickly and effectively into the project team.
The use of new technologies and the setting up of an adequate organisation reaps significant benefits in terms of quality and timeliness.
- Elaboration of the protocol according to Sponsors standards
- Bibliographic Research
- Advice on Methodology / Statistics
- CAP and printing