ISO 9001 is an internationally recognized standard for the effective quality management of businesses in the organization.

     ISO 9001 is quality management system standards. The key concept is the placement of the ISO 9001 management system for quality assurance to ensure that all processes can be controlled and monitored through a system of procedures and working methods. Implementing ISO 9001 to ensure that staffs in the organization knows their responsibilities and working procedures by requires training, knowledge and skills, records as well as monitoring system that is specified in the system or not. The ISO 9001 standard has become the conditions or terms of trade in services between countries. It is also open doors to international trade.

     Presently, the company has been certified ISO 9001: 2015 for all products, included parts and components suppliers also were certified in ISO 9001.

     IATF16949 is a technical specification which aligns for automotive industry aiming to the development of a quality management system that provides for continual improvement, emphasizing defect prevention and the reduction of variation and waste in the supply chain. It is based on the ISO 9001 and additional requirement of customers in the automotive industry. Aim of this standard is to improve the system and process quality to increase customer satisfaction. The requirements are intended to be applied throughout the supply chain or other products within the global automotive industry.

     The company was certified in IATF16949 : 2016, for all products, including relevant division of automotive parts supply was also certified in this standard.

     ISO 13485 is a quality management system that covers the design, development, manufacture, and sale of medical devices. The requirements of this system are applied internationally, such as Europe, Canada, Australia.

     ISO 13485 is based on the process of ISO 9001: 2015 and the developed management system standard for medical device manufacturers.

     The main purpose of this standard is to regulate the medical device industry in accordance with international standards. This standard contains specific requirements for manufacturing, installation and service, which include:

         – The use of several quality management systems has been improved.

         – Guidelines for developing and distributing products with risk management guidelines.

         – Process confirmation

         – Compliance and Regulations

         – Powerful tracking and recall system.

     Aviation Industry Standard Is a quality management system (QMS) standard for the aerospace industry. The current AS9100 Rev B version, made in 2004, incorporates the ISO 9001 standard and additional requirements that are incorporated into the aviation industry.

     ISO/IEC 17025:2017 specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. This standard is for use by laboratories in developing their management system for quality, administrative and technical operations. It covers testing and calibration, record and report.

     The ISO/IEC17025 accredited provides a competitive advantage to all laboratories with reduced costs, establish credibility, improve performance, profits increase and opens the door to the world market, such that there is no need for re-inspection of products in different countries.

     The Material Science Laboratory division and Calibration division of the company has been certified in the ISO/IEC17025: 2017.