EU Medical Device Regulation (EU MDR) News

Check out the latest news and events for EU Medical Device Regulation (EU MDR).

Latest News

  • Amarex, an NSF International Company, Executes Five Rush COVID-19 Related Submissions to the FDA

    • 2 months ago

    GERMANTOWN, Md. – In early March 2020, Amarex Clinical Research LLC, an NSF International company,...

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  • NSF International EVP Kim Trautman Appointed to Regulatory Affairs Professionals Society Board

    • 4 months ago

    ANN ARBOR, Mich. – The Regulatory Affairs Professionals Society (RAPS) has appointed Kim Trautman, Executive...

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  • NSF International Expands Health Sciences Group With Acquisition of Majority Interest in Amarex CRO

    • 8 months ago

    ANN ARBOR, Mich. - Global public health organization NSF International has acquired a majority interest...

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  • Understanding the Japanese Medical Device Approval Process

    • 9 months ago

    Learn about the regulatory approval process required for medical devices to  enter the Japanese market.

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  • NSF International Launches Online Training on Medical Device Regulations for MDSAP Countries

    • 2 years ago

    ANN ARBOR, Mich. – NSF International is the first organization to launch a comprehensive set of...

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  • NSF International Expands Medical Device Consulting Services in Europe With Purchase of PROSYSTEM AG

    • 3 years ago

    ANN ARBOR, Mich., USA and HAMBURG, Germany — NSF International, a global public health and...

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  • NSF Health Sciences Certification, LLC Applies to Become MDSAP Auditing Organization

    • 3 years ago

    ANN ARBOR, Mich. — An application submitted by NSF Health Sciences Certification, LLC, a wholly-owned...

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