When creating a new medical device to the market, there’s much more that goes into designing, developing and introducing it to the market. To be able to enter the certain markets, the development...
Recent Posts
The importance of SW is growing – also in medical devices and as medical devices. This blog text deals with the change of SW’s role, the tightening regulations landscape as well as how to be agile...
Danish company Samplix ApS selected Innokas Medical to co-create the novel Xdrop™ instrument for droplet-based PCR-free enrichment of genomic regions.
“At Innokas Medical, everything begins with the quality built into our processes, products and services. The most important know-how as well as the high standards of our daily operations can be...
Medical devices have remarkably important role in patient care. The key element in the sector is that there cannot be any compromises done with the safety and effectiveness of the devices – the...
Serres Saga® Fluid Management System, co-created by Serres Oy and Innokas Medical, is a smart solution for managing large fluid volumes in the operating rooms, improving efficiency, safety and...
Innokas Design Studio develops software for regulated medical devices to improve peoples' well-being
Healthcare technology is one of the largest high-tech export segments of Finnish industry, and the industry continues to grow strongly year after year. In addition to growth, development is also...
There’s a few common trends in the medical field, which have a clear effect to the development of new medical products. The first one is the constantly changing jungle of rules and regulations,...
In short, Design Controls (or the practices of design and development as in ISO 13485) refers to the application of a set of formal quality practices and procedures to the conduct of product...
MedTech as business is changing and getting more complex. For example, the technical complexity and regulatory requirements are something that are increasing as we speak. In addition, the user...
