Can You Certify an LLM-Driven Medical Device?
Large Language Models (LLMs) such as ChatGPT, Gemini, and Claude are rapidly transforming digital healthcare. From clinical decision support to medical documentation and patient interaction, generativ...
7 Mai 0s
Master UDI-DI: The New Layer Many MedTech Companies Don’t Understand
The implementation of Unique Device Identification (UDI) has already transformed regulatory compliance in the medical device industry. Now, Europe is introducing an additional layer: Master UDI-DI — a...
30 Apr 0s
Life After CE Marking: Why AI Medical Devices Need Continuous Monitoring
Achieving CE marking under the EU MDR is a major milestone for medical device manufacturers. However, for AI-based medical devices, certification is not the end of the journey — it […] The post Life A...
22 Apr 0s
The Fake QMS Problem: Why Your ISO 13485 System Will Fail an Audit
Many medical device companies believe they have a compliant Quality Management System (QMS). On paper, everything looks perfect:• Procedures are written• Forms are available• Risk management is docume...
16 Apr 0s
AI Medical Devices: What Notified Bodies Really Look For
Artificial Intelligence is rapidly transforming the medical device industry, enabling smarter diagnostics, predictive analytics, and personalized healthcare solutions. However, with this innovation co...
8 Apr 0s
Medical Device News APRIL 2026 Regulatory Update
Medboard EU UK Events RoW Your advertisement must contain: For example, you must not: Podcast Service The post Medical Device News APRIL 2026 Regulatory Update appeared first on Medical Device made Ea...
1 Apr 0s
These 3 podcasts will change how you see MedTech
The medical device industry is evolving rapidly, driven by stricter regulations, innovation, and global market challenges.To help you stay ahead, we’ve gathered the most valuable insights from three M...
26 Mar 0s
EUDAMED Deadline 2026 – 7 Steps Every MedTech Company Must Prepare
The upcoming EUDAMED deadline on May 28, 2026, marks a major shift in how regulatory data is managed under the EU MDR and IVDR. While many companies believe this transition […] The post EUDAMED Deadli...
19 Mar 0s
