ARTICLE SUMMARY:
A recent guideline from MedTech Europe seeks to explain how companies can comply with a distinctive element of the EU’s impending unique device identification requirements. That is this month’s “Doc of the Month,” curated from Pathways’ Document Depot.
In our “Docs of the Month” series, we spotlight key items from Pathways’ Document Depot—our running global inventory of medtech regulatory and policy documents—and provide useful details and context. This month, we dig into “MedTech Europe Guidance for Assigning Basic UDI-DI,” which was issued June 2 by the trade association MedTech Europe.
