Quality is one of the main pillar of VISIA LAB

Each project stems from the need to satisfy customer requests, and is developed ensuring precision, reliability, safety, in compliance with the highest quality standards and every applicable regulatory requirements.

All the processes and activities that lead to the creation of our products are planned, executed and monitored according to the principles of quality and the regulatory requirements that govern the complex sector of medical & diagnostic devices, with a view to continuous improvement.

A multidisciplinary team, which involves experienced quality and regulatory personnel in every phase of the project, is the key to obtaining technologically advanced, safe and effective products, which satisfy the customer from all points of view: qualitative, technical and compliance with current regulations.

The training and constant updating of personnel are strategic activities and essential conditions for the achievement of continuous improvement within the company and for the achievement of quality objectives.

Each employee is involved, motivated and sensitized in order to ensure the highest level of quality in the execution of the relevant process phases.


The VISIA LAB Quality Management System complies with the following internationally recognized standards:

EN ISO 13485: 2016

For the European market, our products are CE IVD marked according to current regulations and tested according to the applicable industry standards (IEC 61010, IEC 61326 etc.) for electrical safety and electromagnetic compatibility by accredited laboratories. We are able to support any other kind of non-EU product standard.