The internationally recognised ISO 13485:2003 standard for the manufacture of medical devices was granted following a 12 month programme to develop the Electronic Manufacturing Services (EMS) facilities within the Guangdong Province of China, which now includes a class 10,000 clean room, medical documentation control and fully audited traceability system.
ISO 13485 is a complement to the ISO 9001 Quality, ISO 14001 Environmental and TS16949 Automotive standards already in place and adds considerable value to the Stadium Asia offering in the high reliability and high technology medical sector
- Published: 28 July 2008
- Written by newsprovider