Across industries, the pace to introduce new products is increasing. This puts pressure to shortening the design and development cycles. Medical devices are no exception in this respect.
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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
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 of the...
UKK Terveyspalvelut Ltd., 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 continues internationalization; the company has entered into an agreement with Swedish medtech company Alcosystems AB. The agreement brought yet another Swedish customer to Innokas,...
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. In...
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...
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 idea,...
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 into...
