AQUILAB - Quality Policy

Quality Policy

AQUILAB gives a major importance for the implementation of its Quality Policy, which allows AQUILAB to propose to its customers, in a constant way, safe, reliable, innovative, and effective software and hardware products.

Our employees strive to provide quality products and superior technical support based on the quality management system we have implemented. Our quality management system meets the requirements of the ISO 9001:2008 and ISO 13485:2003 standards for medical device manufacturers.

Executive management ensures that this policy is:
      * Suitable to the organization,
      * Communicated to and understood by all employees,
      * Periodically reviewed to ensure that the effectiveness of the quality management system is maintained.

Our software, ARTISCAN and ARTIVIEW, are declared corresponding to the requirements of the Annex II, section 5 of the Council Directive 93/42/EEC + Amm, 2007/47/EC concerning class IIa medical devices.
This is certified by the certificate CE n° 01-195 delivered on December 20th, 2010 by Bureau Veritas CPS Germany Gmbh (Notified Body 2004).