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Event invitation - Optimal regulatory and design development from idea to success of a medical device

To succeed in taking a medical device product from idea to the market, both the design and development flow, as well as the regulatory flow, need to be considered. As the inventor or manufacturer of...

Design and manufacturing co-operation solves problems – Belgium MedTech meetup report

We all want to see into the future; would you like to predict what kind of problems you could run into during electromechanical device manufacturing process well before those problems happen? While...

Problems and solutions in MDR transition – Innokas Medical at Health Valley Event

Innokas Medical is present at the Health Valley Event (HVE) that will take place on March 30 with the theme of affordable and accessible healthcare supported by technological innovations. Make sure...

Meaningfulness as a value - Tallinn factory employee perspective

Jelena Gladõseva is nearing her third-year milestone working at Innokas Medical’s Tallinn location. The location is a volume-producing factory that has been in operation for over ten years. Jelena...

Ramp-up as a specialty – The benefits of an experienced manufacturing partner in Europe

Whether there is a design of electromechanical device that is still in its working phases or a product that already has a history of being produced at another location, ramp-up can be a challenging...

Recap of the Arab Health Exhibition – Sustainability in Healthcare

As our team took part in Arab Health in Dubai, they were keeping their ears and eyes open for new trends in the industry. The special interest was to see whether issues of sustainability are...

The Future of HealthTech – Dream Further

Walking on the streets of almost any city, we can see that there are quite a bunch of building sites, cranes, and upcoming wonderful colors on the walls of new hospitals enabling more modern...

What to consider when designing a vital signs monitor

Since 2014, Innokas has been manufacturing VC150 Vital Signs Monitor, a device that has also been designed by our Design Studio. VC150 Vital Signs Monitor is used for sub-acute vitals’ monitoring in...

Specialist’s insight – How to tackle the changes within the transition periods of regulations?

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...

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