Medical Device News – September 2021 Latest Updates

Medical Device News – September 2021 Latest Updates

On this September 2021 update we will talk about FDA, MHRA, Swissmedic, ANSM, Fimea, MDCG guidances, New Notified Bodies... A lot to talk about so don't miss this update. If you are not willing to read the guidances, let me summarize it for you.

The post Medical Device News – September 2021 Latest Updates appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

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The FDA Clearance Journey: What Nobody Tells Medical Device Startups

The FDA Clearance Journey: What Nobody Tells Medical Device Startups

For many medical device startups, obtaining FDA clearance seems like a clear, linear process. Identify a predicate device. Prepare your documentation. Submit your application. Wait for clearance. In r...

16 Heinä 0s

The Audit Went Perfectly… So Why Are We Still in Trouble?

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...

9 Heinä 0s

Medical Device News July 2026 Regulatory Update

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...

2 Heinä 0s

“We’ve Never Had a Complaint” — The Most Dangerous Sentence in Medical Devices

“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 ...

25 Kesä 0s

NC vs CAPA: Are You Opening the Wrong Records?

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...

17 Kesä 0s

Best of „AI CE marking“

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...

11 Kesä 0s

Medical Device News June 2026 Regulatory Update

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 

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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