Medical Device Cybersecurity – The Latest Challenges

The FDA in April issued new, detailed draft guidance for the cybersecurity of pre-market medical devices. The document included proposals for how manufacturers should address security risk as part of their submissions for the FDA to give market approval for new products. What is the FDA expecting from manufacturers when it comes to enhancing medical device cybersecurity?

See Also: The Operationalization of Threat Intelligence Programs

This session will examine:

  • Changes in FDA 's cyber expectations from medical device vendors, and why
  • Cybersecurity improvements some medical device manufacturers are already making
  • What do healthcare entities expect from medical device vendors and want from regulators

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