Our experienced team is available for:

  1. Managing your regulatory packs.

    Submissions to CEC, CA, CNIL and CNOM.

  2. Conducting your clinical trials.

    Study feasibility.

    Study coordination (Clinical Trial Manager position).

    Performing monitoring activities (from site selection to site close-out).
    Investigators and Site staff GCP training.

  3. Supporting sites in selecting patients.

    Paper or e CRF completion, scheduling of patient’s visits and assessments, patient pre-screening…

  4. Initiating surveys/questionnaires with physicians.

    On site or remotely.

  5. Some of us are Study Nurses as well, or closely work with Study Nurses located in the same area.

    Study Nurses can perform according to the study schedule of assessments, technical nursing procedures and services: blood samples with or without centrifugation, shipment of samples to central laboratories, monitoring of blood pressure, ECG.

    They can also complete patient questionnaires or CRFs based on source documents.

We offer you : Reactivity, Efficiency, Saving, Self-reliance, Meeting of deadlines, Transparency, Confidentiality.

You identify among our team the Clinical Research Associates (CRAs) you wish to work with.

We draft a cost estimate and write a contractor agreement.

Some Clinical Research Associates (CRAs) can travel in France or in other countries.

Your trial becomes our trial.