A new survey by Asimily has identified that persistent visibility gaps and internal process breakdowns are among the top ...
FDA loosens data rules for medical devices by allowing real-world evidence without patient identifiers in marketing submissions.
The FDA said it plans to accept new forms of real-world evidence in product applications, starting with a subset of medical ...
The healthcare industry is in the middle of a technology revolution, and at the same time, rising health care costs and an aging population are straining the world’s health care infrastructure. To ...
The resin is the first grade in Sabic’s polycarbonate (PC) copolymer portfolio to be formulated without fluorine or other ...
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FDA rarely forces manufacturers to recall dangerous medical devices, GAO report says
The FDA rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it's ...
Shanghai Kohope Medical Devices Co., Ltd. invests $2.5 million in facility expansion hub to meet surging demand for syringes ...
Disrupting the status quo can be an unpredictable, even threatening endeavor for leaders in any business. Nowhere is it more true and prevalent than in healthcare today, and in the medical device ...
Since the 2017 publication of the medical device regulation (MDR) and the IVD regulation (IVDR), EU regulations for medical ...
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