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 →This blog series discusses the Medical Device Regulation (MDR) in brief and how it affects software development for medical devices. In this second part we will discuss the conformity assessment routes, software modules...
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...
Read the article →One of the benefits of automation is, that time of employees is saved for the actual research work, which means cost savings and increased meaningfulness of work.
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