Everyone is familiar with phones, microwaves, and coffee makers, but few people understand what goes into developing these types of devices and the challenges faced when transitioning from a working...
Recent Posts
There are two distinct company types with different starting points when they begin searching for suitable European contract manufacturer. The first is a new start-up in search of their first...
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...
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...
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...
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...
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...
The aim is to develop products as well as possible – high-quality, reliable, easy to use, and cost-effective to manufacture. However, wishes and goals do not always meet, and some things must be...
Innokas Medical launched a service called MDR Fast Track earlier this year. The service enables MedTech companies to enter markets faster with reasonable effort and acceptable risk by outsourcing the...
