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HIMSS 2022 Europe – Three Days of Health, Care & Wellbeing

The hot topics in HIMSS (Healthcare Information and Management Systems Society) Europe exhibition in Helsinki were human centricity and how to enable easier connectivity and interoperability with...

Our new strategy shows in 2022 HIMSS in Helsinki June 14-16th

Last year Innokas launched a new strategy to seek strong growth. This means we are extending our presence into new market areas as well as developing our services and launching new ones. In 2022 we...

The MDR Fast Track service enables MedTech companies to reach the market faster by outsourcing the regulatory burden

Innokas Medical, a Finnish technology company specializing in medical technology, is launching an outsourced responsible manufacturer service for companies striving to reach the highly regulated...

MDR is here!

Long-awaited moment finally happened in May, as after a one-year delay the European Union's new Medical Device Regulation (MDR) came into force. We at Innokas Medical are well-prepared for the MDR...

We help you to master your Medical Device compliance journey!

Professional Quality and Regulatory Services guiding You to master Your Medical Device compliance journey!

Do you feel there's tons of process guidance out there but you don't understand which...

Innokas Medical discusses about the new MDR in Health Tuesday -event

Innokas Medical has been invited to Health Tuesday -event organized by Business Finland, to tell our story how we have implemented the essential European regulatory requirements. Welcome to listen,...

Innokas Medical was chosen as contract supplier with frame agreement on SoteDigi’s MDR consultation project

SoteDigi, who develops new kinds of digital solutions for patient- and health care, selected partner companies for further development of its Omaolo.fi -service solution in the beginning of this...

Innokas Medical’s quality and regulatory services become more diversified

Many medical device design or manufacturing companies may find it difficult to allocate enough time and resources to master the regulatory compliance of medical device, and to compile, maintain, and...

It’s only less than a year to the new European Medical Device Regulations (MDR) – are you ready?

Due to the changes in the medical device legislation in the EU, there’s a lot of things you need to know as a medical device manufacturer. That’s why we decided to start a blog post series in the...

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