Medical device manufacturers
Medical device manufacturers are faced with a rapidly changing business landscape. The role of software is becoming increasingly central to the business strategy. Companies operating in the medical sector risk falling behind unless they start paying close attention to innovations in medical software. From saving time to better patient experiences, digital services will determine who stays on top.
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.
Adapting to changing customer expectations
The role played by medical software has grown in importance and independence. Software is now being integrated into medical devices and other medical systems. The "new" role means there are more requirements to be met by the design and development of medical software: stability and data security first and foremost, but also user-centricity and regulations.
Change drivers in medical business
Medical device manufacturers evolving into SaaS businesses
New commercial models adopted
Patient and caregiver centric solutions needed
Heavy regulations limit the pace of innovation
Digital transformation still ongoing
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.
In our approach to service design, we always focus on the usability and accessibility of the software solutions. Simplified and streamlined workflows in all patient facing activities benefit everyone: the patient, the caregiver and you as the business owner.
Even in this highly regulated environment, it is possible to develop software using agile methodologies. Agile medical SW development is one of the key principles in our medical device quality management system.
Long product lifecycles
We believe that product or system roadmap planning should be done on a portfolio level, transparently by addressing dependencies and timelines. We can help develop automated and connected processes for maintaining your SW products.
Committed talent delivers the best results
There is a high demand for technology and design professionals. Many of them enjoy working on long-term projects where high quality standards are applied and the products serve a higher purpose. We provide our designers and developers with an engaging environment that allows them to grow and thrive, which is reflected in the outcomes of our customer projects.
Many ways to ensure successful medical SW solutions
Development of web, mobile and embedded software
Data, analytics and AI
Cloud services with 24/7 monitoring and support
Patient-centricity using service design
Customer-specific process development based on medical device quality management system
Automated and connected processes and tools for medical SW product development
Explore examples of our work
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