The Audit Went Perfectly… So Why Are We Still in Trouble?
For many medical device companies, a successful audit is seen as the ultimate proof that their Quality Management System is performing well. Few or no findings. Positive feedback from auditors. […] Th...
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Medical Device News July 2026 Regulatory Update
Stay up to date with the latest EU MDR, IVDR, UK MDR and Swiss Medical Device regulations. In this episode we cover: 🤝 Episode Sponsor Medboard 👉 MedBoard – The […] The post Medical Device News July...
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“We’ve Never Had a Complaint” — The Most Dangerous Sentence in Medical Devices
At first glance, hearing “We’ve never had a complaint” sounds like excellent news. No customer dissatisfaction.No product issues.No safety concerns. But for Quality and Regulatory professionals, this ...
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NC vs CAPA: Are You Opening the Wrong Records?
One of the most common sources of confusion in medical device Quality Management Systems is knowing when to open a Nonconformity (NC) and when to initiate a Corrective and Preventive […] The post NC v...
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Best of „AI CE marking“
Artificial intelligence is transforming healthcare, but developing an AI medical device is only part of the challenge. Manufacturers must also navigate certification requirements and maintain safety a...
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Medical Device News June 2026 Regulatory Update
Sponsor Medboard EUROPE UK Easy Medical Device solutions Rest of the World Podcast Easy Medical Device Social Media to follow The post Medical Device News June 2026 Regulatory Update appeared first o...
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FEEDBACK AFTER 3 MONTHS OF THE NEW FDA QMSR IS IN PLACE
The FDA’s new Quality Management System Regulation (QMSR) officially became effective on February 2nd, 2026, replacing the legacy Quality System Regulation (QSR) framework that had been in place for n...
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How can a proper Intended Use save your device?
A medical device’s intended use is not just a regulatory formality — it is the foundation of the entire product strategy. In this podcast episode, Monir El Azzouzi speaks with […] The post How can a p...
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