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Europa Group

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Europa Group provides regulatory and quality affairs consulting services to the medical device industry. They assist companies with navigating the complexities of medical device regulations and achieving market access globally.

Europa Group, as a consultancy, is not a direct manufacturer of medical devices and is therefore not subject to regulations like the FDA 21 CFR Part 820 or EU MDR 2017/745. However, they provide expertise to help their clients meet these regulatory requirements.

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