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Laboratorios SALVAT, S.A. announces that the company’s Quality Management System is certified to the requirements of ISO 13485:2003


ISO 13485 is the international standard for developers and manufacturers of medical devices, and it is frequently used as the framework for quality management systems in terms of ensuring adherence to the regulatory requirements for medical devices (such as CE marking) in various markets.

A company’s ISO 13485 is attained only when a manufacturer has a complete quality management system, and this has been examined and certified by an external, independent auditor (in our case the auditor was ON0318).

The ISO certification acknowledges that Laboratorios SALVAT has been assessed and deemed to comply with the requirements of the ISO standard with respect to the design, development, manufacture and distribution of medical devices. The certification guarantees that all processes at Laboratorios SALVAT are fully controlled and documented and compliant with the company's Quality Management System.

The essence of the ISO 13485 certification is constant monitoring, evaluating, updating, learning and improving. This is what makes the difference between an ISO 13485 certified company and one that is not.

By earning this internationally recognized certification, we offer a product to our customers and suppliers with an additional level of confidence in our quality, reliability, and commitment to continuous improvement.  Laboratorios SALVAT ISO 13485 certification indicates that the highest standards are guaranteed, because we know that you depend on the quality of our products and services.

The ISO 13485 certification has a direct and very positive impact on you, the customer.

Laboratorios SALVAT S.A.
C\ Gall, 30-36 08950 - Esplugues de Llobregat - Barcelona España Tel. +34 933 946 400 Fax. +34 934 732 292
1200 Brickell Avenue, Suite 1950, Miami, FL 33131 (US) Tel. +1 786-528-5273