New Year, New Rules: What to Expect from EU MDR in 2025 The medtech landscape keeps changing, and 2025 marks a pivotal year for EU MDR compliance. Here’s what’s on the horizon: ✅ EUDAMED deadlines: By Q4 2025, mandatory use of specific modules will reshape how companies manage transparency and traceability. ✅ New regulatory updates: Amendments now require manufacturers to inform authorities of supply chain disruptions—adding urgency to strong compliance strategies. ✅ Transitional timelines: While extensions go until 2028 for certain devices, tracking these deadlines is critical to avoid market delays. ✅ Opportunities for growth: Enhanced post-market surveillance and regulatory rigor can build consumer trust and fuel safer, more innovative devices. How prepared is your organization for 2025’s challenges and opportunities? Join regulatory expert Dr. Bassil Akra in our upcoming webinar to cut through the complexities and get your strategy ready for success. https://hubs.ly/Q030MmMr0 ➡️ Ready to stay ahead of EU MDR? Let’s dive into 2025 together.
