Pinja Blog

For example, the company wants to know which equipment are worth investing in and how production should be organized to achieve the best possible efficiency.

In Arnhem, the Netherlands, the Engage 2020 event was held from 2 to 4 March 2020, to which more than 420 customers, partners, and HCL representatives from more than 30 countries gathered to discuss the development and...

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).

In industrial and production environments, it is very typical that processes, roles and responsibilities are very accurately defined.

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...

In the manufacturing industry, a digital twin is an instrument that enables us to prepare for situations and address problems.

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.