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MDR

Redefining Medical Devices in Europe

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MDR

Managing the increasingly intricate regulatory environment of medical device production can be a daunting task. A major example of this is the European Medical Device Regulation (MDR). While it does bring in extra rules that may cause disruptions, it also creates opportunities for the industry. The full life cycle of medical device design and production can take advantage of digital transformation through the LTTS MDR solution, which offers extensive potential to boost innovation and efficiency.

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