Our performing team provides you with:

1. The development of your clinical trials
- Evaluating the feasibility of your studies
- Submissions (CNIL, AFSSAPS, IRB/IEC...)
- Monitoring of your Clinical Trials (starting from evaluation of the investigational sites to the close out visits of the sites)


2 . Helping your investigators in order the enrolment of more patients (paper or e.CRFs data fill in, examinations planning previsions / protocol visits, aid to the pre screening of patients, ...)

3. Setting up Inquiries with Physicians (on site or by telephone).


We guarantee you :

Reactivity,
Efficiency,
Money saving,
Autonomy,
Deadline respect,
Transparency,
Confidentiality.


You are the one who chooses, within our mission, the CRAs you would like to work with. We draw up an estimate for each mission and we can provide you with a financial contract.

Some CRAs can perform business trips on the national or international level.