Skip to content
CEpartner4U
  • Welcome
  • About us
    • Team
    • Jobs
  • Services
    • AR/EC Rep
    • Regulatory affairs
    • Quality system
    • CE/QMS Entry Packages©
    • Clinical evaluation
    • Training
  • UKCApartner4U
  • Information
    • F.A.Q. AR/EC Rep
    • Links
  • Library
  • News
  • Network
  • Contact

About:m.vandervoort

Posts by m.vandervoort :

  • MDCG 2022-2 Guidance on clinical evidence IVDs published, 27 January 2022 in Uncategorized
  • European Commission Press release on IVDR transitional periods, 20 December 2021 in Uncategorized
  • New Regulation about electronic user instructions of medical devices, 15 December 2021 in Uncategorized
  • MedTech Europe issues 2nd edition of the Clinical Evidence Requirements for CE certification under the IVDR, 14 December 2021 in Uncategorized
  • MedTech Europe publishes ‘Use of Symbols to Indicate Compliance with the MDR’ v3.0, 2 December 2021 in Uncategorized
  • European Commission implementing Regulation (EU) 2021/2078 (EUDAMED), 30 November 2021 in Uncategorized
  • MDCG 2021-26 Q&A on re-packaging and re-labelling activities, 21 October 2021 in Uncategorized
  • Press release: European Commission proposes a progressive roll-out of the new IVDR, 14 October 2021 in Uncategorized
  • EUDAMED: 2 new modules available, 4 October 2021 in Uncategorized
  • MDCG 2021-24 Guidance on classification of medical devices, 4 October 2021 in Uncategorized
  • «
  • 1
  • …
  • 7
  • 8
  • 9
  • 10
  • 11
  • 12
  • »

Stay informed

Please check your inbox or spam box to confirm

Copyright 2026 CEpartner4U | Esdoornlaan 13 | 3951 DB Maarn | The Netherlands | +31.6.516.536.26 | office@cepartner4u.com
  • enEnglish