Report written by Innokas experts and event goers Visa Poikela & Päivi Leppänen
Been away from the wet lab for more than 15 years, attending Analytica was an eye-opener. As someone stepping back...
Report written by Innokas experts and event goers Visa Poikela & Päivi Leppänen
Been away from the wet lab for more than 15 years, attending Analytica was an eye-opener. As someone stepping back...
There are two distinct company types with different starting points when they begin searching for suitable European contract manufacturer. The first is a new start-up in search of their first...
Report written by Innokas experts and event goers Päivi Leppänen & Visa Poikela
Contact information available at the end of the post
Sustainability in Medtech was a hot topic. It's clear that the...
If you were asked to picture what good teamwork looks like, how would you picture it? How about a dog sled, traveling with efficient pace and agility through harsh snowy terrain.
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...
Innokas Medical launched a service called MDR Fast Track earlier this year. The service enables MedTech companies to enter markets faster with reasonable effort and acceptable risk by outsourcing the...
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