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Elina Ihme

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Ready or not - the new European Medical Device Regulations (MDR) are coming!

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 NLSD event in Stockholm!

Innokas Medical will participate in Nordic Life Science Days (NLSD) event held in Stockholm, Sweden, at the Waterfront congress center onSeptember 11th-12thInnokas will exhibit at joint stand with...

Innokas Medical’s Scandinavian growth strategy brings yet another customer from Sweden

Swedish health tech innovator Coala Life AB selected Innokas Medical to manufacture Coala Heart Monitor, which has global market potential.

Innokas Medical’s MedTech Design Studio strengthens its expertise in SW and test automation development

The software is becoming more and more important part of medical devices in the future. That’s why it is very crucial for the companies working in the field to be able to develop even more complex...

A long-term co-creation partnership as a common goal for GrainSense and Innokas Medical

Innokas Medical entered into cooperation agreement with Finnish company GrainSense Oy in 2016. The mutual interest for the companies is to develop a long-term, fruitful co-creation partnership, where...

Innokas Medical will participate in NLSD and WHINN fairs in the coming autumn

Innokas will participate in two international trade fairs during the coming autumn: in Nordic Life Science Days (NLSD) event held in Stockholm, Sweden in the beginning of September, and in WHINN...

Finnish health technology exports continue to grow strongly

Healthcare technology is one of the largest high-tech export segments of Finnish industry, and the industry continues to grow strongly. According to the latest export report published by Healthtech...

Ensure the quality compliance of your medical device – learn about the regulatory process in practice

Do you have an idea of a medical device? Or have you already started to develop your medical device? Do you want to enter, e.g., EU or US markets?

FAQs about quality compliance and regulatory affairs in medical business

Finding answers? Welcome! - This is an unofficial guidance which is intended to assist medical device OEMs by answering to some common and basic questions concerning quality compliance and regulatory...

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how to ensure the quality compliance of your medical product

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