Management System Verification

APD strives for excellence in product quality, precise and rapid R&D and manufacturing. We take pride in our timely delivery of products and services. Our continuous refinement of our processes and personnel development has won customer satisfaction and trust. Since the announcement of the new edition of the ISO 9001 international standard, we have continued to pay attention to the changes and requirements of the latest standards. In April 2018, we passed the verification of the new ISO 9001:2015 standard, in addition to maintaining the quality of the products and services consistently provided by APD, while ensuring consistent quality. Through our revision process, the combination of a quality management system and business planning management is promoted.

APD has been cultivating power supply technology for medical products for many years and is committed to building a high quality system. In 2015, it passed the ISO 13485 medical device quality management system (Medical Devices — Quality Management Systems) verification. Each product complies with the stringent requirements of ISO 13485, from regulatory identification and implementation, design management, environmental control, special process control, risk management, traceability, record keeping, etc., to providing a high quality medical power supply for customers.

APD also places emphasis on quality, work environment and employee health and safety and is committed to the monitoring of IECQ QC 080000 Hazardous Substance Process Management (HSPM) System Requirements as well as ISO 14064-1 greenhouse gases inventory. Our data collection and carbon management strategies have been validated by various business organizations over the years and APD has become a qualified supplier to a number of global multinational corporate customers.