Innokas Medical Business Blog

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How to shorten the medical device development cycle in practice?

MedTech business is changing and getting more diverse. The technical complexity, different forms of digitalization and related regulatory requirements are increasing as we speak. And there is the...

Do you want to get competitive edge for your medical device development? Join us for brunch in Copenhagen!

Innokas Medical goes Denmark on 4th April! - Do you want to get competitive edge for your medical device development? Do you know how to ease the burden of regulatory compliance? Do you want to...

Are you ready for stricter rules for software as a medical device under the new MDR in EU? Tips available!

The new Medical Device Regulations (2017/745/EU) (MDR), published in May 2017, will replace the existing Medical Devices Directive (93/42/EEC) (MDD) and the Active Implantable Medical Devices...

Meet Innokas Medical at Digital Health Nordic -event!

Innokas Medical will again participate in Digital Health Nordic -event, which will be held in Helsinki in the beginning of February. The event provides a unique look at the role of technology in...

how to ensure the quality compliance of your medical product

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