MDR - Medical Device Regulation. Regulation of the EU- European Union on the clinical investigation and sale of medical devices for human use. Vector illustration on blue background

How to do business under MDR? A 12-step guide to preparing your company for the new regulations

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The requirements brought in by the Medical Device Regulation have posed a serious challenge for many companies operating in the medical device industry. Adapting to the new legal reality requires a significant amount of time and effort. We have prepared a short guide for the transition process based on the EU recommendations to give you a clearer view of the situation.