The Medical Device Regulation (MDR) aims to harmonize the European market for medical devices.
Read the article →"Recently, I started work as a developer for the Evondos® medication dispensing service system. I find this very meaningful work in many ways”, says Minna Lehtomäki. As a software designer, my duty is to analyze...
Read the article →This blog series discusses the Medical Device Regulation (MDR) in brief and how it affects software development for medical devices. This part discusses the effects of the MDR on your Quality Management System (QMS).
Read the article →In industrial and production environments, it is very typical that processes, roles and responsibilities are very accurately defined.
Read the article →Industrial operating environments change quickly. For a long time, it has been said that change is constant and must be taken into account in the activities. Nevertheless, hardly anyone has been able to prepare for the...
Read the article →In the manufacturing industry, a digital twin is an instrument that enables us to prepare for situations and address problems.
Read the article →With integrations, systems can be made to effectively communicate with each other and data can be transferred at the right time to the right system.
Read the article →Ideally, Power BI guides the activities of the company and the entire personnel towards a more successful future. The vision is wonderful, but why does the system deployment still sometimes fail?
Read the article →This blog series discusses the Medical Device Regulation (MDR) in brief and how it affects software development for medical devices. In this first part we will look at the MDR in brief and the software qualification and...
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