Ville Korpi
June 15 2021
To stand out in the global competition, wholesale and retail companies need to tap into process and customer data and think about the value they can extract from analytics.
For manufacturers, true digital transformation starts by envisioning where in the value chain can data be applied to make a difference.
All public sector services should be designed to serve citizens first. Digital solutions and applications must be easy to use, despite physical and cognitive disabilities.
Digital processes and data-led services help energy and utility sector companies develop a stable energy offering with transparent, customer-centric services.
Shared platforms offer fast entry to new markets, cost-efficiently and scalably. But lasting value add comes from cross-industry collaboration and linking products with complimentary services.
Digitally disrupted, the companies in the banking, finance and insurance sector must actively innovate new approaches to build omnichannel customer experiences that fully utilize data.
While medical device software is strictly regulated, there's room for innovations that make life easier for patients and caregivers. Stable and secure data flow is a must.
June 15 2021
Vincit has implemented dozens of projects for companies operating in the healthcare industry as well as the public sector. The certification allows us to deepen product development cooperation with medical device manufacturers by enabling outsourcing of entire software development parts of medical projects to Vincit.
ISO 13485 certification strengthens Vincit's role as a product development partner and also enables the growth of international business in the medical device industry. The quality management system has been built, where applicable, to use Vincit's existing ISO 9001 management system, which brings Vincit's extensive software design and development expertise to medical device projects.
The certificate covers the design and development of contract-based embedded software for medical devices and in addition, the design and development of stand-alone and cloud-based medical software for the health technology and pharmaceutical industries for both public and private sector healthcare providers. The aim of the certification is also to bring agile development methods, data driven development and software know-how into the regulated health technology industry.
High-quality design and development of medical devices requires a management system based on the ISO 13485 standard. The standard complies with EU regulations for medical devices and helps device manufacturers reduce device risks and improve their reliability. The certified ISO 13485 quality management system ensures that the tools, processes and measures used in the medical software projects comply with the health service regulations, and helps to ensure production of high-quality and safe medical devices.
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