Although Princeton, N.J.-based Guerbet, LLC offers a comprehensive suite of imaging products, equipment service is never far from company executives’ minds. Here, Thomas Ferrari, Guerbet’s Commercial Head of Service of North America, sits down with 24×7 Magazine to discuss why a hybrid service model is one he wholeheartedly endorses.
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The global pacemakers market is projected to surge from its current $4.4 billion valuation to $4.9 billion by 2023, at a CAGR of 2%, according to a new report. This market is driven by various factors such as the increasing prevalence of cardiovascular diseases and technological advancements in medical devices, researchers say.
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In this edition of A Day in the Life, John Weimert, director of biomedical engineering at Texas Children’s Hospital, sits down with 24×7 Magazine to discuss the workload his department handles and how his team has taken a proactive approach to staffing.
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U.S. FDA Commissioner Scott Gottlieb, MD, and Jeff Shuren, MD, director of the Center for Devices and Radiological Health, have announced steps to modernize the FDA’s 510(k) program. Specifically, they’re looking to retire what they consider to be “outdated” criteria.
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Earlier this year, the U.S. FDA released its Medical Device Safety Action Plan, which outlined actions to enhance medical device safety and efficacy. Following public feedback, the agency is announcing a series of updates to encourage innovations that lead to safer medical devices.
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