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Conformity assessment and CE marking – get your new Medical Device to the market under new European Medical Device Regulation

In our previous MDR related blog post we discussed on how to ensure that your existing products are compliant with the new medical device regulation. Now we’re sharing some tips on how to get ready...

Innokas Medical joins the movement - #GivingTuesday as Tuesday’s theme at Innokas

#GivingTuesday is a global day when the world comes together to give.

Cubist digitalizes the healthcare of tomorrow

Serres Group and Innokas Medical continue to strengthen their co-creation strategy and position in Scandinavia when Serres Group launches a new cooperation company in Sweden. Cubist IT AB is acting...

A unique industry requires unique skills – medical device design and development in regulated world

Medical device industry is commonly characterized as regulated domain. Before introducing new medical devices to the market, there’s much more than simply coming up with an innovative idea, building...


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