We support you in the implementation of a software-lifecycle process in accordance with IEC 62304:2006+A1:2015 and IEC 82304-1:2016 to fulfill regulatory and normative documentation requirements. Our specialists support you during the development of software and the preparation of technical documentation including the risk management process and usability for medical software. Our test engineers validate your medical device and process software on site or in our state-of-the-art facilities. We can also perform complete software development according to your specifications.