Insights from recent episode analysis
Audience Interest
Podcast Focus
Publishing Consistency
Platform Reach
Insights are generated by CastFox AI using publicly available data, episode content, and proprietary models.
Most discussed topics
Brands & references
Total monthly reach
Estimated from 6 chart positions in 6 markets.
By chart position
- 🇰🇷KR · Entrepreneurship#1011K to 10K
- 🇸🇪SE · Entrepreneurship#1961K to 10K
- 🇮🇸IS · Entrepreneurship#1530K to 100K
- 🇮🇱IL · Entrepreneurship#903K to 10K
- 🇰🇪KE · Entrepreneurship#149500 to 3K
- Per-Episode Audience
Est. listeners per new episode within ~30 days
11K to 41K🎙 Daily cadence·396 episodes·Last published yesterday - Monthly Reach
Unique listeners across all episodes (30 days)
36K to 136K🇮🇸74%🇰🇷7%🇸🇪7%+3 more - Active Followers
Loyal subscribers who consistently listen
14K to 54K
Market Insights
Platform Distribution
Reach across major podcast platforms, updated hourly
Total Followers
—
Total Plays
—
Total Reviews
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* Data sourced directly from platform APIs and aggregated hourly across all major podcast directories.
On the show
From 15 epsHost
Recent guests
Recent episodes
“We’ve Never Had a Complaint” — The Most Dangerous Sentence in Medical Devices
Jun 25, 2026
NC vs CAPA: Are You Opening the Wrong Records?
Jun 17, 2026
Best of „AI CE marking“
Jun 11, 2026
Medical Device News June 2026 Regulatory Update
Jun 3, 2026
FEEDBACK AFTER 3 MONTHS OF THE NEW FDA QMSR IS IN PLACE
May 28, 2026
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| Date | Episode | Topics | Guests | Brands | Places | Keywords | Sponsor | Length | |
|---|---|---|---|---|---|---|---|---|---|
| 6/25/26 |  “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 statement should trigger […] The post “We’ve Never Had a Complaint” — The Most Dangerous Sentence in Medical Devices appeared first on Medical Device made Easy Podcast. hamza benafqir | — | ||||||
| 6/17/26 | 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 vs CAPA: Are You Opening the Wrong Records? appeared first on Medical Device made Easy Podcast. hamza benafqir | — | ||||||
| 6/11/26 | Best of „AI CE marking“✨ | artificial intelligencemedical devices+3 | — | AICE marking+1 | — | AICE marking+5 | — | — | |
| 6/3/26 | Medical Device News June 2026 Regulatory Update✨ | regulatory updatesmedical devices+1 | — | Easy Medical Device | — | medical deviceregulatory update+3 | Medboard EUROPE UK | — | |
| 5/28/26 | FEEDBACK AFTER 3 MONTHS OF THE NEW FDA QMSR IS IN PLACE✨ | FDA regulationsQuality Management System+4 | — | FDA | — | FDAQMSR+5 | — | — | |
| 5/21/26 | How can a proper Intended Use save your device?✨ | intended usemedical device strategy+3 | — | — | — | intended usemedical device+3 | — | — | |
| 5/13/26 | Medical Device News May 2026 Regulatory Update✨ | regulatory updatesmedical devices+3 | — | — | EuropeSwitzerland+1 | medical deviceregulatory update+5 | — | — | |
| 5/7/26 | Can You Certify an LLM-Driven Medical Device?✨ | UDI mistakesmedical devices+3 | — | ChatGPTGemini+2 | — | UDImedical devices+4 | — | — | |
| 4/30/26 | Master UDI-DI: The New Layer Many MedTech Companies Don’t Understand✨ | Unique Device Identificationregulatory compliance+3 | — | EuropeUnique Device Identification (UDI)+2 | — | UDIMaster UDI-DI+3 | — | — | |
| 4/22/26 | Life After CE Marking: Why AI Medical Devices Need Continuous Monitoring✨ | CE markingAI medical devices+3 | — | EU MDR | — | CE markingAI medical devices+4 | — | — | |
Want analysis for the episodes below?Free for Pro Submit a request, we'll have your selected episodes analyzed within an hour. Free, at no cost to you, for Pro users. | |||||||||
| 4/16/26 | The Fake QMS Problem: Why Your ISO 13485 System Will Fail an Audit✨ | Quality Management SystemISO 13485+4 | — | ISO 13485 | — | Quality Management SystemISO 13485+5 | — | — | |
| 4/8/26 | AI Medical Devices: What Notified Bodies Really Look For✨ | Artificial Intelligencemedical devices+4 | Camille | Medical Device made Easy Podcast | — | AImedical devices+5 | — | — | |
| 4/1/26 | Medical Device News APRIL 2026 Regulatory Update✨ | regulatory updatesmedical devices+3 | — | Medboard | EUUK+1 | medical deviceregulatory update+5 | — | — | |
| 3/26/26 | These 3 podcasts will change how you see MedTech✨ | medical device industrypodcast insights+1 | — | MedTech | — | MedTechmedical device+4 | — | — | |
| 3/19/26 | EUDAMED Deadline 2026 – 7 Steps Every MedTech Company Must Prepare✨ | EUDAMEDregulatory data+5 | — | EU MDRIVDR | — | EUDAMEDMedTech+5 | — | — | |
| 3/13/26 | Medical Device News March 2026 Regulatory Update✨ | regulatory updatesmedical devices+1 | — | Medboard EuropeNB UK Solutions+1 | — | medical deviceregulatory update+3 | — | — | |
| 3/5/26 | IMDRF & Regulatory Reliance Explained: The Future of Global Medical Device Approvals✨ | regulatory environmentmedical device approvals+3 | — | IMDRF | — | medical devicesregulatory reliance+4 | — | — | |
| 2/26/26 | 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 | — | ||||||
| 2/19/26 | 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 | — | ||||||
| 2/11/26 | 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 | — | ||||||
| 2/5/26 | Validation & Supplier Management in MedTech | Validation is a cornerstone of medical device compliance — yet it remains one of the most challenging areas for manufacturers. In this podcast episode, Simon Foeger, Founder of SIFO MEDICAL, […] The post Validation & Supplier Management in MedTech appeared first on Medical Device made Easy Podcast. hamza benafqir | — | ||||||
| 1/28/26 | QMSR Is Coming: Why FDA Inspections Will Change Completely in 2026 | For decades, medical device manufacturers in the US relied on 21 CFR 820 (QSR) — a system known for being procedural and checklist-oriented.But starting February 2nd, 2026, FDA will implement […] The post QMSR Is Coming: Why FDA Inspections Will Change Completely in 2026 appeared first on Medical Device made Easy Podcast. hamza benafqir | — | ||||||
| 1/22/26 | How to Remediate a Design History File (DHF) | Design History File (DHF) remediation is rarely planned — yet it is a recurring challenge for many medical device manufacturers, especially during audits, inspections, acquisitions, or regulatory framework changes. In […] The post How to Remediate a Design History File (DHF) appeared first on Medical Device made Easy Podcast. hamza benafqir | — | ||||||
| 1/15/26 | Medical Device News January 2026 Regulatory Update | Social Media to follow The post Medical Device News January 2026 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir | — | ||||||
| 1/7/26 | Verification & Validation Explained — A Practical Conversation with Aaron Joseph | Verification & Validation (V&V) plays a central role in ensuring that medical devices are safe, effective, and compliant — yet it remains one of the most challenging phases for many […] The post Verification & Validation Explained — A Practical Conversation with Aaron Joseph appeared first on Medical Device made Easy Podcast. hamza benafqir | — | ||||||
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Chart Positions
7 placements across 6 markets.
Chart Positions
7 placements across 6 markets.