The role of software in medical devices used to be considered rather insignificant. Software simply existed in order to enable devices to be used and for data to be obtained. It was seen as a component of a system, not as an actual service that provides business benefits and value. All that is now changing.
Focusing on sustainable value production in medical software
To gain value from new software solutions in the medical segment, the design and development of software needs to account for many things. Firstly, the regulatory environment. Then, stability, data security and user-centricity.
Better patient experiences, sustainable business value
With the help of our user-centric service design, you can deliver a much better experience for your patients and speed up the time used by caregivers in inputting data. Of course advanced medical software needs to be regularly updated to account for industry best practices and changes in governmental regulations. Only commitment to continuous improvements can deliver lasting value for your business.
Let's design secure and user-centric software for medical devices
At Vincit, we have the experience required to design software solutions for this highly regulated environment. Our development processes have been audited for ISO 9001 and we have a quality management system that has been granted the ISO-13485 certificate, qualifying us to develop medical device software.