Jelena Gladõseva is nearing her third-year milestone working at Innokas Medical’s Tallinn location. The location is a volume-producing factory that has been in operation for over ten years. Jelena...
Recent Posts
Whether there is a design of electromechanical device that is still in its working phases or a product that already has a history of being produced at another location, ramp-up can be a challenging...
As our team took part in Arab Health in Dubai, they were keeping their ears and eyes open for new trends in the industry. The special interest was to see whether issues of sustainability are...
Walking on the streets of almost any city, we can see that there are quite a bunch of building sites, cranes, and upcoming wonderful colors on the walls of new hospitals enabling more modern...
Since 2014, Innokas has been manufacturing VC150 Vital Signs Monitor, a device that has also been designed by our Design Studio. VC150 Vital Signs Monitor is used for sub-acute vitals’ monitoring in...
Manufacturers who have devices CE Marked to the directives MDD, AIMDD or IVDD (i.e., legacy devices) have deadlines for regulatory compliance if they want to keep their devices on the European...
We are proud to announce that Innokas Medical is taking part in Circular Design training program.
In 2022, Technology Industries Finland challenged companies to hire experts from among international students. The goal of the campaign was to give the students Finnish working life experience,...
The new MDR regulation has expanded the need for clinical evaluation in companies designing medical devices. The interview for my master's thesis highlighted the requirements set by the new...
