MDR & Drug-Device Combination Products with Theresa Jeary

MDR & Drug-Device Combination Products with Theresa Jeary

Did you know that the EU MDR is amending 2001/83/EC for Medicinal Products. This may have some consequences for your products if it involves a Drug-Device combination. Monir El Azzouzi and Theresa Jeary are explaining to you what should be done.

The post MDR & Drug-Device Combination Products with Theresa Jeary appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Det här avsnittet är hämtat från ett öppet RSS-flöde och publiceras inte av Podme. Det kan innehålla reklam.

Avsnitt(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 Juli 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 Juli 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 Juni 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 Juni 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 Juni 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 Juni 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 Maj 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 Maj 0s

Populärt inom Business & ekonomi

badfluence
framgangspodden
varvet
dynastin
rss-borsens-finest
uppgang-och-fall
avanzapodden
svd-tech-brief
rss-inga-dumma-fragor-om-pengar
fill-or-kill
bathina-en-podcast
rss-dagen-med-di
tabberaset
borslunch-2
rikatillsammans-om-privatekonomi-rikedom-i-livet
rss-kort-lang-analyspodden-fran-di
market-makers
rss-hos-psykologen
rss-borslunch
rss-veckans-trade