Proceeding according to a certified quality management system not only offers the opportunity of manufacturing high quality medical devices in an optimized and efficient manner, but also represents a competitive advantage and a precondition for the international acceptance of a company.
  Quality management systems not only become more important for manufacturers of medical devices, but also for suppliers and distributors. For manufacturers of medical devices of classes IIa, IIb and III a quality management system is even obligatory.

On the way to the CE marking of medical devices the European Testing Center of Medical Devices PMG may offer the certification of quality management systems to its customers. The PMG certifies quality management systems according to EN ISO 13485 for active medical devices including their accessories. On request a quality management system may also be certified according to EN ISO 9001.