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To remain FDA compliant, all medical devices must have labels that contain a unique device identification (UDI) – a number that makes them..

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The FDA has passed legislation requiring all medical devices to have a unique device identification (UDI) number to make them recognizable..

UDI, All

To manage regulatory requirements, companies in government regulated industries — especially life sciences — need an enterprise resource..

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In 2007, the government passed the Food and Drug Administration Amendments Act (FDAAA). This act required the Food and Drug Administration..

UDI, All

Managing compliance requirements is a concern for a variety of industries, and remaining up to date with state and federal regulations..

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The FDA, regulatory compliance requirements, challenging timetables, and strict quality assurance needs are only a few of the hurdles ..

UDI, Sage X3, Sage Enterprise Management, All

The United States has the largest medical device market in the world, spending more than $150 billion dollars on medical devices each year...

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As a medical device manufacturer, you're faced with some of the most challenging demands in business. Then, if you factor in the need to..

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