Medical device industry has been one of our key customer segments, and we want to serve this segment even better in the future. We want to ensure that the quality of our components and assemblies meet the demands of high-end medical devices. That is why we have established a development project, partly funded by Business Finland, to investigate how we need to adjust our procedures to meet the demands of the ISO 13485 standard. This standard sets out the requirements for a quality management system specific to the medical device industry. Safety and quality are non-negotiable in the medical device industry, and therefore we want to work towards certifying our quality for this segment. As the requirement of certificates along the supply chain is ever increasing both by clients and by authorities, the ISO 13485 would help us secure our competitivity and growth as the market recovers from the COVID-19 recession.