The European Society of Cardiology says medical device oversight in Europe is not sufficient, and is calling for a single European regulatory body to oversee product evaluation and approval.
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Manufacturers of medical products would be foolish to think that recent upheavals at the US FDA will result in a lack of inspections in the coming years. A panel of experts discussed the current state of inspections during a webinar hosted by the Food and Drug Law Institute.
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An interactive look at recent executive-level company changes and promotions in the medical device and diagnostics industries.
