The complexity of medical device cybersecurity requirements: How to cope
Mitigating cybersecurity risks for medical devices is increasingly a core focus area for regulators, who are driving the establishment of a consistent cybersecurity framework to better facilitate coordination among all parties involved. This emphasizes the importance of Medical Device Manufacturers (MDMs) being aware of and familiar with the latest requirements. The intertwining of requirements, however, creates significant complexity in the medical device cybersecurity ecosystem. How can you cope with this?
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