If your company produces medical or health-related products, you need to know whether they meet the FDA’s definition of Class I medical devices—and, if so, you need to start now to implement UDI Rule requirements before enforcement begins on September 24.
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In this Soapbox column, Massachusetts General Hospital Systems Engineering Manager Rick Schrenker talks risk management files, delving into what you need to know about them and why.
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The Institute for Safe Medication Practices (ISMP) has published updated guidelines to help healthcare practitioners maximize the intended safety benefits of smart infusion pumps and better position their organizations for bi-directional interoperability with the electronic health record.
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CE CYBER Academy will give TRIMEDX’s associates—more than 3,100 nationwide—the vital skills that many health systems struggle to source in the face of unprecedented demand for cybersecurity expertise.
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A team of researchers at the Helmholtz-Zentrum Geesthacht in Germany has established a method to quickly and reliably predict the degradation of polymer materials with sophisticated molecular architectures.
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