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MedTech Europe slams EU over lack of preparation for MDR/IVDR

November 26, 2019 By Nancy Crotti

With six months to go before the EU’s new Medical Device Regulation takes effect, Europe’s medtech trade association is accusing government authorities of dragging their feet on the process.

MedTech Europe said that the industry is trying to prepare but that it remains “seriously held back by the slow and piecemeal implementation” of the new regulatory framework.

Get the full story on our sister site, MassDevice.

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  • Home
  • Medical Device Business
    • Mergers & Acquisitions
    • Financial
    • Regulatory
  • Applications
    • Cardiovascular
    • Devices
    • Imaging
    • Implantables
    • Medical Equipment
    • Orthopedic
    • Surgical
  • Technologies
    • Contract Manufacturing
    • Components
    • Electronics
    • Extrusions
    • Materials
    • Motion Control
    • Prototyping
    • Pumps
    • Tubing
  • Med Tech Resources
    • Subscribe to Print Magazine
    • DeviceTalks Tuesdays
    • Digital Editions
    • eBooks
    • Manufacturer Search
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    • MedTech 100 Index
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    • Print Subscription
    • The Big 100
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    • Video
  • 2022 Leadership in MedTech
    • 2022 Leadership Voting!
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  • Women in Medtech