Helen Simmons
Quality Specialist

Cambridge Design Partnership

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Helen Simmons is a Quality Specialist at CDP.

Contributions

DOES THE NEW EU MDR SPELL THE END OF GRANDFATHERING?

Helen Simons and Stephanie Ward describe how the new EU Medical Devices Regulation will impact on “grandfathered” devices that were approved under old regulation and are currently on the market, but do not necessarily comply with current/updated regulatory standards, and explain the potential implications for device manufacturers.

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