The ongoing digitization in healthcare has brought not only new opportunities to improve patient care, but also challenges in cybersecurity. To address the issue and ensure the security of new medical devices, state-of-the-art regulatory frameworks are mandatory. Let’s discover some of the new industry developments, discuss the best practice documents and the implementation of the guidance.
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With the rise of the Internet of Medical Things (IoMT), medical devices are becoming increasingly more prominent in the healthcare industry. This, however, does not come without its risks. Hackers are using medical devices to springboard deeper into medical system networks. This article explores the motives as well as the methods used to access medical devices.
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Threat modeling, in recent years has come to take center stage in the world of healthcare cybersecurity. The FDA has been helping medical device manufacturers ramp-up their skills in this field, however it still remains a complex task to perform for newer manufacturers. Let’s explore the challenges, current state of practice and the right approach.
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To secure against potential cybersecurity vulnerabilities, Medical Device Manufacturers (MDMs) should enroll their medical devices into a Public Key Infrastructure (PKI), a trusted and widely used cryptographic practice that ensures operational safety. Learn more about securing your medical device with a PKI from our free e-book: “Why should Medical Device Manufacturers (MDMs) secure their devices with a Public Key Infrastructure (PKI)?”
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Are you overwhelmed with all the MedTech regulatory acronyms? Don’t worry, we are here to help! We’ve broken it down and addressed the why, the how and the where to give you a better understanding of the field.
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With the Medical Device Regulation (MDR) requirements being already 12 months old, how do you make sure of your compliance with medical device cybersecurity going forward?
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When two FDA cybersecurity leaders highlight the importance of threat modeling for more secure medical devices, it’s time to pay close attention. Find out why they’re saying it’s vital to device design and approval.
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