Keyword: Health and welfare technology

Medical device manufacturers have long been following the timeline of the implementation obligations of the MDR and the predecessor MDD. The EU still has not announced an exact date for the end of MDD support, but it is...

Projects related to medical devices are a special entity of Pinja’s diverse software development projects. The software development of these projects must take into account, among other things, the EU MDR regulation,...

Sustainability is first and foremost about action. At Pinja, we make our biggest sustainability contributions together with our clients by driving digitalization and streamlining our clients’ businesses across a myriad...

In addition to enjoying the summer and the sun, it is nice to read something every once in a while. So, we put together a reading and viewing package for you on the most popular topics of the year. We wish you inspiring...

The Medical Device Regulation (MDR) aims to harmonize the European market for medical devices.

"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...

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).

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...