Learn Post Market Surveillance with Natasha Bankowski

Learn Post Market Surveillance with Natasha Bankowski

On this episode I invited Natasha Bankowski that is also called the PMS Queen to help us understand the Post Marketing Surveillance for Medical Devices. You can also meet her at TOPRA Symposium 2019.

The post Learn Post Market Surveillance with Natasha Bankowski appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Denne episoden er hentet fra en åpen RSS-feed og er ikke publisert av Podme. Den kan derfor inneholde annonser.

Episoder(404)

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

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...

28 Mai 0s

How can a proper Intended Use save your device?

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...

21 Mai 0s

Populært innen Business og økonomi

stopp-verden
lydartikler-fra-aftenposten
dine-penger-pengeradet
e24-podden
rss-penger-polser-og-politikk
rss-borsmorgen-okonominyhetene
rss-skravla-gar
pengepodden-2
livet-pa-veien-med-jan-erik-larssen
finansredaksjonen
utbytte
okonomiamatorene
rss-pa-konto
tid-er-penger-en-podcast-med-peter-warren
morgenkaffen-med-finansavisen
liberal-halvtime
lederpodden
pengesnakk
rss-impressions-2
stormkast-med-valebrokk-stordalen