Institutions and Healthcare professionals

Benefit from an operational assistance on investigational sites in order to optimize with efficiency the performance of your industrial clinical trials, in full respect of patients rights.

We also advise you on the optimization of your internal Quality management processes in order to make your site a reference point for excellence in Clinical Research.

We also perform independant audits (internal audits, external audits, or GCP focused...)

Pharma Industry and CROs

We advise and assist your clinical investigationnal sites experiencing difficulties.

We perform quality controls of investigationnal sites and Inspection readiness trainings and support for Regulatory Inspections.

We also advise you on the optimization and compliance of your quality processes, in respect with local and international regulations and are able to perform quality management systems audits or GCP focused.