MedTech business is changing and getting more diverse. The technical complexity, caused mainly by digitization, is increasing. New technologies are being introduced at faster pace, the impact of...
Recent Posts
FlowOx 2.0, developed in co-creation between Norwegian company Otivio AS and Innokas Medical, has now reached a significant milestone as the device has received CE mark and the sales has started. The...
Innokas Medical strengthens its expertise in project management and software development and testing
Innokas Medical has further reinforced its know-how in medical device design and development. Two new resources have joined Innokas’ SW development team, while the teams of project managers,...
Pekka Patja, who has led Innokas Medical’s sourcing and manufacturing businesses since 2015, decided to leave his duties during the winter. Thus, Innokas Medical has appointed Ari Paalijärvi (B.Eng.)...
Innokas Medical will participate in the Health Talks event to be held in Tampere, Finland, on March 19th. During the afternoon, the light on the mystical world of medical device regulations (MDRs)...
Innokas Medical will be visiting International Dental Show (a.k.a IDS), which will be held in Cologne, Germany, from 12th to 16th March, 2019! IDS is the leading global trade fair for the dental...
MedTech business is changing and getting more diverse. The technical complexity, different forms of digitalization and related regulatory requirements are increasing as we speak. And there is the...
Innokas Medical goes Denmark on 4th April! - Do you want to get competitive edge for your medical device development? Do you know how to ease the burden of regulatory compliance? Do you want to learn...
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...
