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Tag: eu authorized representative medical device

Home eu authorized representative medical device

Managing EU Authorized Representative Requirement – EU MDR

By Waqas Imam0 CommentsGeneral
Medical device manufacturing organizations are scattered all around the globe. Some of them are localized into countries, while others have managed to spread their operations globally, and many are still struggling to do so. Those medical device manufacturing organizations that want to expand their operations in Europe have to comply…
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TSQ Asia & Middle East is well positioned for providing support in Medical Device field. We are a European company ISO 13485:2016 Certified extending support with local presence in Middle East and Asia to help business leaders with daily challenges in device Product Development and QA/RA matters.
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  • Home
  • QMS Support
    • ISO Management System
    • Trainings – ISO & Regulatory Affairs (Medical & Pharmaceuticals)
    • MDSAP – Medical Device Single Audit Program
    • Usability & HFE
    • VMP IQ/OQ/PQ Validation
  • Regulatory Support
    • MDR 2017/745
    • Medical Devices EU Compliance & Regulatory Support
    • EU Design Approval Support
    • Medical Devices Registration to South America
  • CE MARK
  • EU Auth. Rep.
  • UKCA
  • Contact US