Are you ready to roll up your sleeves and show us what you got? Are you willing to challenge yourself and achieve better and better results with high quality medical device products? If you [...]
When you’re working in medical industry, it’s a fact that regulations and standards are something that companies need to follow and they’re coming stricter for everyone continuously. This is [...]
An agile co-creation of next generation medical devices – Innokas launches the MedTech Design Studio
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Innokas Medical renewed its strategy during the last year, aiming to achieve the company’s new vision and to take the changes of the operative environment as well as the development needs [...]
UKK Terveyspalvelut Oy, whose headquarters are located in Tampere Finland, is working with an important matter: together with its main owner, the UKK Institute, the company promotes the [...]
Innokas Medical gets a new customer in Scandinavia: manufacturing contract signed with Swedish company Alcosystems AB
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Innokas Medical continues internationalization; the company has entered into an agreement with Swedish medtech company Alcosystems AB. The agreement brought yet another Swedish customer to [...]
Innokas Medical’s key figures for 2017 show that the constantly increasing competition in the field did not have a significant impact on Innokas; the company managed to increase its turnover. [...]
Collaboration between Innokas Medical and Kasve – promoting the success of medical device OEMs in the market
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Innokas Medical and Kasve Ltd. have agreed on strategic partnership in Nordic countries. Kasve is a Finnish expert service company located in Kuopio, focused e.g. on the quality and regulatory [...]
Tips available! How to balance the regulatory compliance with medical device design and development process?
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When creating a new medical device to the market, there’s much more that goes into designing, developing, and introducing a medical device to the market than simply coming up with an innovative [...]
Bringing a medical or an IVD device to market can be a nightmare of confusing regulatory standards and regulatory authority certifications that must be complied with and which must be integrated [...]
The jungle of rules and regulations in medical device business – is it a nightmare or a fairy tale?
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The design and manufacturing of medical devices is way more challenging than engineering work and factory production of e.g. consumer electronics. In medical device business, it is not enough to [...]
