Medical Device made Easy Podcast
Learn how to put a compliant Medical Device on the market
Monir El Azzouzi
Show overview
Medical Device made Easy Podcast has been publishing since 2018, and across the 8 years since has built a catalogue of 402 episodes. Releases follow a weekly cadence.
None of the episodes are flagged explicit by the publisher. It is catalogued as a EN-US-language Business show.
The show is actively publishing — the most recent episode landed 4 days ago, with 25 episodes already out so far this year. Published by Monir El Azzouzi.
From the publisher
Listen Medical Device Regulation and Standards
Latest Episodes
View all 402 episodes“We’ve Never Had a Complaint” — The Most Dangerous Sentence in Medical Devices
NC vs CAPA: Are You Opening the Wrong Records?
Best of „AI CE marking“
Medical Device News June 2026 Regulatory Update
FEEDBACK AFTER 3 MONTHS OF THE NEW FDA QMSR IS IN PLACE
How can a proper Intended Use save your device?
Medical Device News May 2026 Regulatory Update
The Hidden Costs of UDI Mistakes in Medical Devices
Master UDI-DI: The New Layer Many MedTech Companies Don’t Understand
Life After CE Marking: Why AI Medical Devices Need Continuous Monitoring
The Fake QMS Problem: Why Your ISO 13485 System Will Fail an Audit
AI Medical Devices: What Notified Bodies Really Look For
Artificial Intelligence is rapidly transforming the medical device industry, enabling smarter diagnostics, predictive analytics, and personalized healthcare solutions. However, with this innovation comes increased regulatory complexity. In this episode, Camille […] The post AI Medical Devices: What Notified Bodies Really Look For appeared first on Medical Device made Easy Podcast. hamza benafqir
Medical Device News APRIL 2026 Regulatory Update
Medboard EU UK Events RoW Your advertisement must contain: For example, you must not: Podcast Service The post Medical Device News APRIL 2026 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir
These 3 podcasts will change how you see MedTech
The medical device industry is evolving rapidly, driven by stricter regulations, innovation, and global market challenges.To help you stay ahead, we’ve gathered the most valuable insights from three MedTech podcasts […] The post These 3 podcasts will change how you see MedTech appeared first on Medical Device made Easy Podcast. hamza benafqir
EUDAMED Deadline 2026 – 7 Steps Every MedTech Company Must Prepare
The upcoming EUDAMED deadline on May 28, 2026, marks a major shift in how regulatory data is managed under the EU MDR and IVDR. While many companies believe this transition […] The post EUDAMED Deadline 2026 – 7 Steps Every MedTech Company Must Prepare appeared first on Medical Device made Easy Podcast. hamza benafqir
Medical Device News March 2026 Regulatory Update
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IMDRF & Regulatory Reliance Explained: The Future of Global Medical Device Approvals
The global medical device regulatory environment is complex, often requiring manufacturers to repeat similar submissions and audits across multiple countries. This duplication slows innovation and delays patient access to life-saving […] The post IMDRF & Regulatory Reliance Explained: The Future of Global Medical Device Approvals appeared first on Medical Device made Easy Podcast. hamza benafqir
IEC 60601 – From 2nd to 4th Edition: What Manufacturers Must Know
IEC 60601 has been central to medical electrical equipment safety for decades. From the prescriptive approach of the 2nd edition to the risk-based philosophy introduced in the 3rd edition, the […] The post IEC 60601 – From 2nd to 4th Edition: What Manufacturers Must Know appeared first on Medical Device made Easy Podcast. hamza benafqir
Defect Management in SaMD — From Chaos to Control
In Software as a Medical Device (SaMD), defect management is far more than tracking bugs. It is a structured, risk-driven process that directly impacts patient safety, regulatory compliance, and product […] The post Defect Management in SaMD — From Chaos to Control appeared first on Medical Device made Easy Podcast. hamza benafqir
Medical Device News February 2026 Regulatory Update
SPONSOR EUROPE  New Harmonization Standards –  Implementing Decision 2026/193:  The conference will feature three breakout sessions focusing on: Switzerland UK Training EasyIFU RoW North America APAC Africa: https://eservicesdata.edaegypt.gov.eg/MedicalDevices Middle East […] The post Medical Device News February 2026 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir