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SALVAT News


Laboratorios SALVAT, S.A. announces that its Quality Management System has been certified as meeting ISO 13485:2003 requirements

09/03/12

ISO 13485 is the international standard for developers and manufacturers of medical devices and is often used as a framework for Quality Management Systems that guarantee compliance with the regulatory requirements for medical devices (for example, the «CE» mark) in different markets.

ISO 13485 accreditation is only achieved when a manufacturer has a full Quality Management System in place and has been inspected and certified by an independent external auditor (in our case the auditor was ON0318).

The ISO certification recognizes that Laboratorios SALVAT has been assessed and complies with the ISO standard requirements in terms of design, development, manufacture and distribution of medical devices. The certification guarantees that all the Laboratorios SALVAT processes are fully controlled and documented and carried out in accordance with the Quality Management System.

The essence of the ISO 13485 certification is constant monitoring, evaluation, updating, training and improvement of processes. This marks the difference between a company which has ISO 13485 certification and one which does not.

Having secured this internationally-recognized certification, we are able to offer our customers and partners a product with an added level of confidence in our quality, reliability and commitment to continuous improvement. The ISO 13485 certification of Laboratorios SALVAT indicates that the highest standards are guaranteed, since we know that you depend on the quality of our products and services. 

The ISO certification 13485 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 salvat@svt.com
1200 Brickell Avenue, Suite 1950, Miami, FL 33131 (US) Tel. +1 786-528-5273 salvatusa@svt.com