Clean Room Assembly Services

MET’s subcontract clean room production is uniquely supported by our ISO 17025 accredited QA laboratory. The on-site support includes medical device design performance validation, packaging validation and quality assurance processes. The clean room is state of the art, ISO class 7 with filtration cabinets offering even higher cleanliness levels. In addition to ISO 9001 and ISO 17025 MET is audited to ISO 13485.

Some of MET’s engineers were have been working in medical device development since the 1980’s. We have experience across a wide range of devices and applications in terms of engineering, materials and regulations.