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Medical Device Cybersecurity Risks & Best Practices: Navigating the Nuanced Cyber Regulatory Waters
Smart medical devices have underlying cybersecurity and privacy risks. They are also top targets from a host of global attackers from nation states to sophisticated criminal gangs. The health sector — including medical device manufacturers as well as pharmaceutical and biotech companies — faces uncharted regulatory and liability risks.
FDAnews has invited global cybersecurity expert Norma Krayem to walk you through the rapidly changing global regulatory landscape and show you new coping strategies.
Over the course of 90 fast-paced minutes, Ms. Krayem will move from the Cybersecurity Executive Order 13800 to HIPAA, Homeland Security and more:
With U.S. agencies — FDA, HHS, DHS — all at work on new sector risk bulletins and re-evaluation of current rules such as HIPAA, and global regulators equally involved, this is a pressing matter. Address it now, by committing an hour and a half of your time to this timely learning session.
Cybersecurity is a multi-discipline activity, so team participation in the presentation is important. Team members include:
Norma Krayem, Sr. Policy Advisor and Co-Chair, Cybersecurity and Privacy Team, Holland & Knight
Norma is a well-known cybersecurity expert in a host of sectors including health and understands the global regulatory structure for medical devices. She will talk about the current and emerging regulatory environment and discuss the nexus of cyber risk to the Internet of Things (IoT) as well which will impact the medical device industry. She is regularly sought out by the media, policy and elected officials around the world on cyber risk.
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