The first question related to one that was asked here on the Club a while ago
A question that would be great for the community to elaborate on some more as Milan didn’t have direct experience in medical device regulation
What type/approach of quality assurance should apply to MDR (Medical Device Regulations) compliant software?
The question we didn’t get to although we did discuss access to production logs so perhaps this has already answered the question?
Is it possible to get telemetry data or usage metrics from production to help with development, testing and business decisions?