Medical devices manufacturing
Why
The role of software in medical devices used to be minimal – software simply existed in order to allow the use of devices and obtain data. That’s now changing as software is seen as an actual service that provides business benefits and value.
Key industry challenges
Medical device manufacturers are evolving into software as a service (SaaS) businesses
New commercial models adopted
Patient and caregiver-centric solutions needed
Heavy regulations limit the pace of innovation
What
To gain value from new software solutions in the medical segment, the design and development of software needs to account for many things. Number one is the regulatory environment. Then, stability, data security, and user-centricity need to be taken into account.
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. Advanced medical software needs to be regularly updated to account for industry best practices and changes in governmental regulations.
How
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 an ISO-13485 certificate, meaning we’re qualified to develop medical device software.
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01.
User-centric design
In our approach to service design, we always focus on the usability and accessibility of the software solutions. Simplified and streamlined workflows benefit everyone: the patient, the caregiver, and you as the business owner.
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02.
Agile R&D
Even in this highly regulated environment, it’s possible to develop software using agile methodologies.
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03.
Long product lifecycles
We believe that product or system roadmap planning should be done on a portfolio level by addressing dependencies and timelines. We can help develop automated processes for maintaining your software products.