The U.S. Food & Drug Administration issued select updates to premarket cybersecurity guidance including who is required to comply, the types of devices that fall under certain agency requirements and recommendations on how to…
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Earlier this week, the government announced its plan to tackle ethnic and other biases in medical devices, in a bid to position the UK as a world leader on the topic. The plan follows…
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ORLANDO – During the HIMSS24 panel discussion “Securing the Modern Connected Hospital,” James Angle, product manager of information security at Trinity Health, and hacktivist for hire Kevin Johnson, chief executive officer at Secure Ideas,…
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Philips introduces the Silent Patient Room, a revolutionary concept aimed at humanizing hospital environments, particularly in the ICU. Through seamless integration of diverse medical devices and innovative communication channels, this solution prioritizes patient comfort…
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The U.S. National Cybersecurity Strategy, announced in March 2023, was joined by several other regulatory and legislative initiatives throughout the year that will have a major impact on the security of the Internet of…
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EarSwitch has been selected for the UK’s Innovative Devices Access Pathway pilot, a programme which aims to accelerate access to innovative medical devices for the NHS.The pilot has selected eight devices for its programme,…
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Intellectual property can be a thorny issue in health tech and medtech. The intersection of healthcare data and AI is setting up some complex patent showdowns and interesting ethical discussions. What are the implications…
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Mary Russell, MJ BS RN, Sr. Director, Clinical Services, CliniComp The types of medical devices available and their use in patient care continue to accelerate. The medical devices market is anticipated to surpass $656B…
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The UK government has made a multi-million pound investment in potential breakthrough medical devices. As part of a £10 million funding package for boosting access to medical technology, eight innovative tech companies will be supported…
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Moderate-risk medical devices constitute 99% of those that have been regulated by the U.S. Food and Drug Administration (FDA) since it gained authority to regulate medical technology nearly five decades ago. This article presents…
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