Quarem Resources

After years of phased delays and voluntary participation, four core EUDAMED modules become mandatory under EU MDR and IVDR on May 28, 2026. For manufacturers, importers, and EU Authorized Representatives, this is a hard regulatory deadline, not a guideline. What's changing? The European Commission's EUDAMED database was designed to consolidate device identification, certification, and surveillance data across the EU single market. As of May 28, the following four modules move