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EU MDR (The European Union Medical Device Regulation) is a regulatory framework that applies to all European medical device manufacturers to establish high quality and safety standards for medical devices production.
In the modern world, the life sciences sector is going through a period of unprecedented regulatory change affecting organizations involved in pharmaceuticals, medical devices, and in-vitro diagnostics. The European Union Medical Device Regulation (EU MDR), a robust, transparent, predictable and sustainable regulatory framework for medical devices, ensures high standards of quality and safety being produced in or supplied into Europe.
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