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The medical device industry is one of the most highly regulated industries out there.
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Lately, there’s been quite the buzz around the European Union Medical Device Regulation or better known as, EU MDR. The EU MDR is a priority for all companies in the medical device industry that distribute products in the EU and will officially take effect on May 26, 2021. This regulation has more need for data management and complex assessment procedures than the regulation it replaces (MDD – Medical Devices Directive).
Imagine a world without color - pretty boring, right?
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Imagine hand drawing floor plans for the Empire State Building before AutoCAD was developed; if you made a mistake, you often had to start from scratch, the process took forever, and the risk for errors was high.
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