Obtaining CE marking for a medical device

The Clinical Operations Department recommends the drafting of clinical investigation plans that answer the requirements of the new European regulation in relation to the prerequisites of the French or European Personal Protection Committees.

Even for retrospective studies, we recommend it to make sure that the methodological approach of the investigation has been mastered.

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    RGPD – Protection of your data

    Our references

    ELSAN
    Bioprojet
    Allecra
    CHU Nantes