Although the full impact of COVID-19 is uncertain, one sure thing is that industry continues to crave information to help them navigate EU MDR.
Once a cost to the business, now field service is re-writing the rules for healthcare organizations.
It’s time for medtech design engineers to take a page from the enterprise security playbook.
Designers and manufacturers of both devices and software must conduct due diligence and ensure regulatory compliance in protecting user data.
A look at the pros and cons of connected medical devices.
When a software patch or device update cannot remedy a cyber threat, sometimes a recall is necessary.