Quality system

Voxcan performs preclinical studies in a context of Good Laboratory Practice (GLP) edicted by OECD and FDA requirements concerning electronic records (21 CFR Part.11).

In order to create a robust link with our customers and meet the quality requirements of regulatory authorities, we put all our efforts to be compliant with OECD and FDA requirements to perform preclinical activities.

By this way we consider ALCOA data management as a reference to ensure data integrity.

Traceability and training of employees are daily integrated into the management of the studies and the human resources. Voxcan’s personnel is certified through a rigorous internal training program work.