Medical device regulations include requirements with which both the device and their manufacturer need to comply to enable legal market entry. However, these requirements are often vaque, described...
Recent Posts
Innokas Medical will join Lääketietokeskus' online event on March 16th, where the regulatory requirements of medical devices outside the EU will be discussed. Our talented Linda Kellberg (Specialist,...
Together with our cooperation partner Swedish Medtech we would like to discuss about Clinical Evaluation of Medical Device Software. Thus, we've been invited to hold an online event with Swedish...
