Clean Room Assembly Services
MET CLEAN ROOM DIVISION
MET provide clean room assembly services with excellence in medical device assembly and packaging. Specialising in small and unusual production runs we can provide your clinical trial quantity production and early stage product delivery.
Our team have been working in medical devices for many years. We know about manufacture, packaging, regulation, quality, performance, development, supply chain, safety and much more.
Our assembly and packaging clean room is 'state of the art' ISO Class 7 (class 10,000, GMP EU Grade C), it is thoughtfully laid out for maximum efficiency and controlled under ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes.
All this is supported by our ISO 17025 accredited laboratory divisions: device performance testing, material analysis, and packaging validation.
MET's engineers and scientists can support your product through all medical device product phases right from your earliest ideas. Our experience of development, risk analysis and prototyping can help get you off the ground. Our scientists can test prototypes and validate production processes. Our deep knowledge will smooth your path through all your regulatory needs.
Download and read the Excellence in Clean Room Assembly Services information sheet.