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  • Start Now
  • About
  • Customers
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  • Login
  • More +
    • What is CE marking?
    • Benefits of CE marking?
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    • Can you do CE marking Self-Certification?
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    • What does CE certification cost?
    • Who is responsible for CE marking?
    • Amazon Responsible Person for CE-marked products
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AI

French & German warning: EU must extend MDR transition period

French & German warning: EU must extend MDR transition period

The French and the Germans warn: The EU must extend MDR transition period. This comes following a meeting with European Commission representatives in Paris on March 14, 2022. 

Categories News Tags AI, CE Marking, EU, European Commission, European harmonized standards, market surveillance, mdr, MDR transition, medical devices

Compliance And The Growth Of The Medical Industry

Compliance and the growth of the medical industry, does it collaborate?

Compliance and the growth of the medical industry, does it work together? This question is highly relevant because the growth in the medical device industry is significant. And also, this will continue to be the case for the foreseeable future.

Categories Agency Insight, Articles, Medical Devices Directive, News Tags AI, compliance, medical devices, medical regulations, MedTech

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  • New IVDR Notified Body in Slovakia
  • MDCG Publishes IVDR Guidelines MDCG 2022-6
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  • Start Now
  • About
  • Customers
  • Blog
  • Login
  • More +
    • What is CE marking?
    • Benefits of CE marking?
    • Does your product need CE?
    • Can you do CE marking Self-Certification?
    • Which countries require the CE mark?
    • What does CE certification cost?
    • Who is responsible for CE marking?
    • Amazon Responsible Person for CE-marked products
    • CE Marking Directives and Regulations
    • Technical File
    • EU Declaration of Conformity