ISO 9001
Checking that the system works is a vital part of ISO 9001:2015. It is recommended that an organization performs internal audits to check how its quality management system is working. An organization may decide to invite an independent certification body to verify that it is in conformity to the standard, but there is no requirement for this. Alternatively, it might invite its clients to audit the quality system for themselves.[/vc_column_text][/vc_column][/vc_row][vc_row][vc_column][vc_separator style=”dotted” border_width=”2″ css=”.vc_custom_1502733653622{padding-top: 10px !important;padding-bottom: 10px !important;}”][/vc_column][/vc_row][vc_row][vc_column width=”1/4″][vc_single_image image=”5838″ img_size=”full”][/vc_column][vc_column width=”3/4″][vc_column_text]
TS 16949
The ISO/TS16949 is an ISO technical specification aimed at the development of a quality management system that provides for continual improvement, emphasizing defectprevention and the reduction of variation and waste in the automotive industry supply chain.[/vc_column_text][/vc_column][/vc_row][vc_row][vc_column][vc_separator style=”dotted” border_width=”2″ css=”.vc_custom_1502733662158{padding-top: 10px !important;padding-bottom: 10px !important;}”][/vc_column][/vc_row][vc_row][vc_column width=”1/4″][vc_single_image image=”5837″ img_size=”full”][/vc_column][vc_column width=”3/4″][vc_column_text]
ISO 14001
ISO 14001:2015 sets out the criteria for an environmental management system and can be certified to. It maps out a framework that a company or organization can follow to set up an effective environmental management system. It can be used by any organization regardless of its activity or sector. It can provide assurance to company management and employees as well as external stakeholders that environmental impact is being measured and improved.[/vc_column_text][/vc_column][/vc_row][vc_row][vc_column][vc_separator style=”dotted” border_width=”2″ css=”.vc_custom_1502733662158{padding-top: 10px !important;padding-bottom: 10px !important;}”][/vc_column][/vc_row][vc_row][vc_column width=”1/4″][vc_single_image image=”5836″ img_size=”full”][/vc_column][vc_column width=”3/4″][vc_column_text]
ISO 13485
Safety and quality are non-negotiables in the medical devices industry. Regulatory requirements are increasingly stringent throughout every step of a product’s life cycle, including service and delivery. More and more, organizations in the industry are expected to demonstrate their quality management processes and ensure best practice in everything they do.[/vc_column_text][/vc_column][/vc_row]