How Document Management Systems Help with EU MDR and IVDR...

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2025-07-31 06:07:31 -

How Document Management Systems Help with EU MDR and IVDR Documentation

1. Introduction The EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) present stringent documentation expectations. A modern Document Management Software is essential for managing technical files, risk assessments, validation documents, and post‑market surveillance artifacts, especially in the context of Document Management, document version control software, and...

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