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...
Recent Posts
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...
Innokas Medical strengthens its QA&RA services with a new Clinical Affairs team. The new team supports medical device companies in carrying out resource-binding clinical evaluation related work by...
We R&D engineers often think that the world is ready when a product is launched to the market, and we can move on to developing the next interesting gadget. But in reality, the life of the product is...
This summer, we took part in Kilometrikisa, a playful cycling competition between work communities, departments, organizations, clubs, or any kind of team you want. The purpose is to track down...
Ever since the European Commission published the new regulations for medical and in-vitro diagnostic devices, there have been serious concerns regarding the availability of medical devices and how...
Were you at the Subcontracting fair last week in Tampere? We were and what we experienced was the whole exhibition center full of companies, people, networking, and great discussions. The stands were...
