Team-NB has released Version 3 of its Position Paper on the submission of technical documentation according to Annex II and III of the Medical Device Regulation (EU) 2017/745.
📄 Explore the full Position Paper: https://lnkd.in/d3iSj4va
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- Clinical Evidence Requirements under the EU In Vitro Diagnostics Regulation (IVDR). MEDTECH E-BOOK
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- Manual on borderline and classification for medical devices under Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices Version 4 – September 2025
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