ISO 13485 – the internationally recognized standard for quality management in the medical devices industry – has a lot in common with the requirements of the medical directives. The certification of a quality management system, specifically for medical devices, to ISO 13485 proves advantageous, and in many cases essential, for medical companies which export their products to the global market. A significant portion of demonstrating compliance with the directive requirements is the establishment and independent assessment of the quality system. For more info visit @ http://www.elitecertification.com/iso-13485-certification/ or Call @ +91-9716006477