How to certify your Software as a Medical Device? (SaMD)

How to certify your Software as a Medical Device? (SaMD)

Software as a Medical Device is an area that is exploding. So understanding how this is working and what to be done is important. Listen to this episode to have more clarity on your projects for EU and US.

The post How to certify your Software as a Medical Device? (SaMD) appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

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Episoder(406)

The Audit Readiness Myth: Why Most Startups Aren’t As Prepared As They Think

The Audit Readiness Myth: Why Most Startups Aren’t As Prepared As They Think

Many medical device startups assume they’re audit ready because they have documented procedures, completed templates, and a Quality Management System in place. However, successful audits require much ...

23 Jul 0s

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 Jul 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 Jul 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 Jul 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 Jun 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 Jun 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 Jun 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...

3 Jun 0s

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