Complete set-up and management of a clinical study

In order to validate the efficacy of a product in a clinical study, the writing of a protocol, the selection of investigator sites, the obtaining of regulatory approvals, the management and validation of data, the complete statistical analysis and the writing of the clinical report are required.

 

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    RGPD – Protection of your data

    Our references

    ELSAN
    Bioprojet
    Allecra
    CHU Nantes