EUDAMED Deadlines 2026 Mandatory Modules Explained скачать в хорошем качестве

EUDAMED Deadlines 2026 Mandatory Modules Explained

By May 28, 2026, EUDAMED becomes mandatory and many manufacturers are still unprepared. In this episode of Reg with MEG, we’re joined by MedEnvoy Regulatory Consultant Brittany Dunning to break down: Which EUDAMED modules are mandatory by May 2026 The most common readiness gaps manufacturers face Why Actor Registration and SRN issuance are major bottlenecks How device data quality can block UDI registration What EU Authorized Representatives, importers, and Notified Bodies now expect Practical steps to avoid last-minute delays and market access risk We also discuss how importer verification obligations and Notified Body sequencing are changing — and why coordination across stakeholders is critical. If you’re a medical device or IVD manufacturer preparing for EUDAMED (and swissdamed), this episode provides a clear, practical roadmap to get ready with confidence. 🔔 Subscribe for weekly regulatory updates 📩 Learn more about MedEnvoy’s EUDAMED & registration support at medenvoyglobal.com