Medical Device made Easy Podcast
Medical Device made Easy Podcast

Medical Device made Easy Podcast

easymedicaldevice

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My name is Monir El Azzouzi and I am a Medical Device Expert specialized in Quality and Regulatory affairs. And on this podcast I will help you place compliant medical devices on the market. For that I will share with you my knowledge or the one of others through discussion or interviews. I will invite experts in the area to tell you what you can do or the challenges you may encounter.

Recent Episodes

Medical Device News DECEMBER 2025 Regulatory Update
DEC 11, 2025
Medical Device News DECEMBER 2025 Regulatory Update
<p></p><p><strong>Medboard</strong></p><p></p><p><strong>Europe</strong></p><p></p><p>48% disruption in the EU - I hope you are all healthy: <a href="https://health.ec.europa.eu/document/download/13b2c812-b144-4489-af1f-e76af5bc97fd_en?filename=md_availability_study_presentation_2024.pdf" rel="external nofollow noreferrer noopener" target="_blank">https://health.ec.europa.eu/document/download/13b2c812-b144-4489-af1f-e76af5bc97fd_en?filename=md_availability_study_presentation_2024.pdf</a></p><p></p><p>Consultation: SCHEER asks you - Are Brain Stimulators for non-medical purpose dangerous: <a href="https://health.ec.europa.eu/consultations/scheer-public-consultation-preliminary-scientific-opinion-health-hazards-and-risks-associated-use_en" rel="external nofollow noreferrer noopener" target="_blank">https://health.ec.europa.eu/consultations/scheer-public-consultation-preliminary-scientific-opinion-health-hazards-and-risks-associated-use_en</a></p><p></p><p>Q&amp;A Medicines used with Medical Devices - Revision 6 with new questions: <a href="https://www.ema.europa.eu/en/documents/regulatory-procedural-guideline/questions-answers-implementation-medical-devices-vitro-diagnostic-medical-devices-regulations-eu-2017-745-eu-2017-746_en.pdf" rel="external nofollow noreferrer noopener" target="_blank">https://www.ema.europa.eu/en/documents/regulatory-procedural-guideline/questions-answers-implementation-medical-devices-vitro-diagnostic-medical-devices-regulations-eu-2017-745-eu-2017-746_en.pdf</a></p><p>EUDAMED is Mandatory - From 28 May 2026: <a href="https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202502371%20-%20https://health.ec.europa.eu/latest-updates/eudamed-four-first-modules-will-be-mandatory-use-28-may-2026-2025-11-27_en" rel="external nofollow noreferrer noopener" target="_blank">https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202502371 - https://health.ec.europa.eu/latest-updates/eudamed-four-first-modules-will-be-mandatory-use-28-may-2026-2025-11-27_en</a></p><p><strong>UK</strong></p><p></p><p>Better Call MHRA - But we don't consult: <a href="https://www.gov.uk/guidance/medical-devices-get-regulatory-advice-from-the-mhra" rel="external nofollow noreferrer noopener" target="_blank">https://www.gov.uk/guidance/medical-devices-get-regulatory-advice-from-the-mhra</a></p><p></p><p><strong>Standard</strong></p><p></p><p>ISO 10993-1 mutation - Nothing is automatic anymore: <a href="https://www.youtube.com/watch?v=AkSZVNSz5a0" rel="external nofollow noreferrer noopener" target="_blank">https://www.youtube.com/watch?v=AkSZVNSz5a0</a></p><p>ISO 18969 draft -  Comments until 28-01-2026: <a href="https://www.youtube.com/watch?v=zCR9HlHJ5l0" rel="external nofollow noreferrer noopener" target="_blank">https://www.youtube.com/watch?v=zCR9HlHJ5l0</a></p><p><strong>EasyIFU</strong></p><p></p><p>Create your Labels with EasyIFU - UDI included: <a href="https://easyifu.com" rel="external nofollow noreferrer noopener" target="_blank">https://easyifu.com</a></p><p></p><p><strong>Rest of the World</strong></p><p></p><p><strong>Argentina</strong></p><p></p><p>Argentina: Simplified application - Class I/A or Class II/B: <a href="https://www.argentina.gob.ar/noticias/anmat-establece-un-regimen-simplificado-para-la-habilitacion-de-establecimientos" rel="external nofollow noreferrer noopener" target="_blank">https://www.argentina.gob.ar/noticias/anmat-establece-un-regimen-simplificado-para-la-habilitacion-de-establecimientos</a></p><p></p><p> </p><p></p><p> </p><p></p><p><strong>Canada</strong></p><p></p><p>Canada: Modernization of the MDEL - Some changes: <a href="https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/establishment-licences/medical-devices-compliance-bulletin/consultation-modernizing-mdel-framework-phase-ii.html" rel="external nofollow noreferrer noopener" target="_blank">https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/establishment-licences/medical-devices-compliance-bulletin/consultation-modernizing-mdel-framework-phase-ii.html</a></p><p>Canada: Medical Device License Application - Guidance on how to do it: <a href="https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/managing-applications-licenses.html" rel="external nofollow noreferrer noopener" target="_blank">https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/managing-applications-licenses.html</a></p><p><strong>Brazil</strong></p><p></p><p>Brazil: Digitalisation of Certificates - You can request that online now: <a href="https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2025/anvisa-lanca-nova-ferramenta-para-emitir-certificados-de-dispositivos-medicos" rel="external nofollow noreferrer noopener" target="_blank">https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2025/anvisa-lanca-nova-ferramenta-para-emitir-certificados-de-dispositivos-medicos</a></p><p></p><p><strong>Podcast</strong></p><p></p><p>Podcast Nostalgia - Let's review previous podcasts</p><p></p><p>Episode 363 - The journey of a CRO with Helene Quie: <a href="https://podcast.easymedicaldevice.com/363-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/363-2/</a></p><p></p><p>Episode 364 - What is changing with the new ISO 10993-1 with Marina Daineko: <a href="https://podcast.easymedicaldevice.com/364-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/364-2/</a></p><p></p><p>Episode 365 - How to become a Lead Auditor with Rob Packard: <a href="https://podcast.easymedicaldevice.com/365-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/365-2/</a></p><p></p><p><strong>Social Media to follow</strong></p><p>Monir El Azzouzi Linkedin: <a href="https://linkedin.com/in/melazzouzi" rel="external nofollow noreferrer noopener" target="_blank">https://linkedin.com/in/melazzouzi</a></p><p>Twitter: <a href="https://twitter.com/elazzouzim" rel="external nofollow noreferrer noopener" target="_blank">https://twitter.com/elazzouzim</a></p><p></p><p>Pinterest: <a href="https://www.pinterest.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.pinterest.com/easymedicaldevice</a></p><p></p><p>Instagram: <a href="https://www.instagram.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.instagram.com/easymedicaldevice</a></p><p></p>
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29 MIN
How to become a LEAD AUDITOR made Easy
DEC 4, 2025
How to become a LEAD AUDITOR made Easy
<p></p><p>Becoming a Lead Auditor is one of the most valuable career steps for quality and regulatory professionals in the MedTech sector. Lead Auditors play a critical role in evaluating QMS performance, improving compliance, and preparing organizations for ISO certification.</p><p></p><p>In this podcast episode, we explore:</p><p></p><p><span class="ipsEmoji">🔹</span> What is a Lead Auditor?</p><p></p><p>The responsibilities, authority, and role differences between internal audits, supplier audits, and certification audits.</p><p></p><p><span class="ipsEmoji">🔹</span> Who can become a Lead Auditor?</p><p></p><p>The competencies required, background expectations, and what makes a good auditor.</p><p></p><p><span class="ipsEmoji">🔹</span> What you must learn to be effective:</p><p></p><p>ISO 19011 — the core auditing guideline</p><p></p><p>ISO 13485 — the medical device QMS standard</p><p></p><p>ISO 14971 — risk management for medical devices</p><p></p><p>Software lifecycle &amp; technical documentation considerations</p><p></p><p><span class="ipsEmoji">🔹</span> Do Lead Auditor certificates expire?</p><p></p><p>Clarifying the myth around renewal, competency maintenance, and the expectations of certification bodies.</p><p></p><p><span class="ipsEmoji">🔹</span> Spotlight: Lead Auditor Training by Medical Device Academy</p><p></p><p>We review the upcoming training course, covering:</p><p></p><p>Curriculum and learning objectives</p><p></p><p>Exam format</p><p></p><p>Prerequisites</p><p></p><p>Pricing</p><p></p><p>Training dates</p><p></p><p>Certificate details</p><p></p><p><span class="ipsEmoji">👉</span> Learn more or register here: <a href="https://medicaldeviceacademy.com/lead-auditor-training/" rel="external nofollow noreferrer noopener" target="_blank">https://medicaldeviceacademy.com/lead-auditor-training/</a></p><p></p><p>This episode is ideal for QA/RA specialists, QMS managers, consultants, and anyone aiming to take a leadership role in medical device auditing.</p><p></p><p><strong>Who is Monir El Azzouzi?</strong></p><p></p><p>Monir El Azzouzi is a Medical Device Expert specializing in Quality and Regulatory Affairs. After working for many years with big Healthcare companies, particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people better understand Medical Device Regulations worldwide. He has now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through videos, podcasts, online courses… His company also acts as Authorized Representative for the EU, UK, and Switzerland. Easy Medical Device becomes a one-stop shop for medical device manufacturers that need support on Quality and Regulatory Affairs.</p><p></p><p><strong>Social Media to follow</strong></p><p></p><p>Monir El Azzouzi Linkedin: <a href="https://linkedin.com/in/melazzouzi" rel="external nofollow noreferrer noopener" target="_blank">https://linkedin.com/in/melazzouzi</a></p><p></p><p>Twitter: <a href="https://twitter.com/elazzouzim" rel="external nofollow noreferrer noopener" target="_blank">https://twitter.com/elazzouzim</a></p><p></p><p>Pinterest: <a href="https://www.pinterest.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.pinterest.com/easymedicaldevice</a></p><p></p><p>Instagram: <a href="https://www.instagram.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.instagram.com/easymedicaldevice</a></p><p></p>
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40 MIN
What is changing with the new ISO 10993-1 version 2025 
NOV 27, 2025
What is changing with the new ISO 10993-1 version 2025 
<p></p><p>The long-awaited revision of ISO 10993-1 is almost here – and the MedTech community is full of questions.<br>Will we need to retest everything?<br>Is this a complete game-changer, or just an evolution?<br>How will Notified Bodies and the FDA react?</p><p></p><p>In this episode of the Medical Device Made Easy Podcast, Monir El Azzouzi hosts Marina Daineko, biocompatibility consultant at Intrinsic Medical Group, to unpack what’s really coming.</p><p></p><p>This episode covers:</p><p></p><p>The background and current status of the ISO 10993-1 revision</p><p></p><p>Why the new version is best seen as an evolution, not a revolution</p><p></p><p>How the standard pushes further into a risk-based, scientifically justified approach</p><p></p><p>The link with ISO 14971 and lifecycle thinking</p><p></p><p>Changes in contact categorization and cumulative exposure</p><p></p><p>The industry trend toward reducing animal testing through in vitro methods and data-driven justification</p><p></p><p>How to conduct a gap analysis once the new standard is published</p><p></p><p>Practical advice on how to prioritize updates without freezing projects or panicking</p><p></p><p>Real-world examples where process chemicals, not base materials, changed the risk picture</p><p></p><p>How Intrinsic Medical Group supports companies with biological evaluation, cleanliness, sterilization and reusable devices</p><p></p><p><span class="ipsEmoji">👉</span> If you’re involved in RA/QA, R&amp;D, toxicology, or clinical development, this conversation gives you a practical roadmap for navigating the transition to the new ISO 10993-1.</p><p></p><p><strong>Who is Monir El Azzouzi?</strong></p><p></p><p>Monir El Azzouzi is a Medical Device Expert specializing in Quality and Regulatory Affairs. After working for many years with big Healthcare companies, particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people better understand Medical Device Regulations worldwide. He has now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through videos, podcasts, online courses… His company also acts as Authorized Representative for the EU, UK, and Switzerland. Easy Medical Device becomes a one-stop shop for medical device manufacturers that need support on Quality and Regulatory Affairs.</p><p></p><p><strong>Links</strong></p><p></p><p>Marina Daineko Linkedin: <a href="https://www.linkedin.com/in/marinadaineko/" rel="external nofollow noreferrer noopener" target="_blank">https://www.linkedin.com/in/marinadaineko/</a></p><p></p><p>Intrinsic Medical Group, LLC: <a href="https://www.linkedin.com/company/intrinsic-medical-group/posts/?feedView=all" rel="external nofollow noreferrer noopener" target="_blank">https://www.linkedin.com/company/intrinsic-medical-group/posts/?feedView=all</a></p><p></p><p><strong>Social Media to follow</strong></p><p></p><p>Monir El Azzouzi Linkedin: <a href="https://linkedin.com/in/melazzouzi" rel="external nofollow noreferrer noopener" target="_blank">https://linkedin.com/in/melazzouzi</a></p><p></p><p>Twitter: <a href="https://twitter.com/elazzouzim" rel="external nofollow noreferrer noopener" target="_blank">https://twitter.com/elazzouzim</a></p><p></p><p>Pinterest: <a href="https://www.pinterest.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.pinterest.com/easymedicaldevice</a></p><p></p><p>Instagram: <a href="https://www.instagram.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.instagram.com/easymedicaldevice</a></p><p></p>
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37 MIN
From Zero to One: The journey of a CRO with Helene Quie
NOV 20, 2025
From Zero to One: The journey of a CRO with Helene Quie
<p>In this long-form interview, Helene Quie, founder of Qmed Consulting, shares an inside look at nearly 20 years of experience in clinical and regulatory consulting for medical devices.</p><p>This article covers:</p><ul><li>Helene’s personal journey from employee to entrepreneur</li><li>The early risks and decisions that shaped Qmed’s growth</li><li>How the company’s services and markets evolved over time</li><li>A deep dive into clinical evidence generation vs equivalence</li><li>The seismic impact of EU MDR on clinical strategies</li><li>PMCF pitfalls and real-life examples</li><li>Working with Notified Bodies and new expectations under MDR</li><li>Lessons from projects that didn’t go as planned</li><li>The crucial alignment between clinical data and human factors</li><li>Practical advice for startups on avoiding top regulatory mistakes</li><li>Her vision of the future: RWE, adaptive study designs, digital health &amp; greater regulatory convergence</li></ul><p><strong>Links:</strong></p><p>Helene Quie: <a href="https://www.linkedin.com/in/helene-quie-863a323/" rel="external nofollow noreferrer noopener" target="_blank">https://www.linkedin.com/in/helene-quie-863a323/</a></p><p>Qmed Consulting: <a href="https://qmed-consulting.com/" rel="external nofollow noreferrer noopener" target="_blank">https://qmed-consulting.com/</a></p><p><strong>Who is Monir El Azzouzi?</strong></p><p>Monir El Azzouzi is a Medical Device Expert specializing in Quality and Regulatory Affairs. After working for many years with big Healthcare companies, particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people better understand Medical Device Regulations worldwide. He has now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through videos, podcasts, online courses… His company also acts as Authorized Representative for the EU, UK, and Switzerland. Easy Medical Device becomes a one-stop shop for medical device manufacturers that need support on Quality and Regulatory Affairs.</p><p><strong>Social Media to follow</strong></p><p>Monir El Azzouzi Linkedin: <a href="https://linkedin.com/in/melazzouzi" rel="external nofollow noreferrer noopener" target="_blank">https://linkedin.com/in/melazzouzi</a></p><p>Twitter: <a href="https://twitter.com/elazzouzim" rel="external nofollow noreferrer noopener" target="_blank">https://twitter.com/elazzouzim</a></p><p>Pinterest: <a href="https://www.pinterest.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.pinterest.com/easymedicaldevice</a></p><p>Instagram: <a href="https://www.instagram.com/easymedicaldevice" rel="external nofollow noreferrer noopener" target="_blank">https://www.instagram.com/easymedicaldevice</a></p>
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58 MIN
Medical Device News November 2025 Regulatory Update
NOV 12, 2025
Medical Device News November 2025 Regulatory Update
<p><strong>MedBoard</strong></p><p> </p><p><strong>EU</strong></p><p>Joint clinical assessment procedure -  EU 2025/2086 regulation for reimbursement in the EU: <a href="https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202502086" rel="external nofollow noreferrer noopener" target="_blank">https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202502086</a></p><p>Team-NB position paper on Companion diagnostics - Significant changes rules: <a href="https://www.team-nb.org/wp-content/uploads/2025/10/Team-NB-PositionPaper-IVDR-Significant-changes-V2.pdf" rel="external nofollow noreferrer noopener" target="_blank">https://www.team-nb.org/wp-content/uploads/2025/10/Team-NB-PositionPaper-IVDR-Significant-changes-V2.pdf</a></p><p>MDR and IVDR put at risk transplantation - Donor Screening and SoHo preparation: <a href="https://www.edqm.eu/documents/52006/162284/PA-PH-TO%20%2824%29%2018%20%E2%80%93%20Risks%20to%20safety%20and%20quality%20in%20donor%20screening%20and%20SoHO%20preparations%20due%20to%20poor%20implementation%20of%20the%20MDR%20and%20IVDR%20%E2%80%93%20CD-P-TO%20Position%20paper%20%E2%80%93%20October%202025.pdf/51d5efb2-4611-13ad-76a0-b5710b371248" rel="external nofollow noreferrer noopener" target="_blank">https://www.edqm.eu/documents/52006/162284/PA-PH-TO%20%2824%29%2018%20%E2%80%93%20Risks%20to%20safety%20and%20quality%20in%20donor%20screening%20and%20SoHO%20preparations%20due%20to%20poor%20implementation%20of%20the%20MDR%20and%20IVDR%20%E2%80%93%20CD-P-TO%20Position%20paper%20%E2%80%93%20October%202025.pdf/51d5efb2-4611-13ad-76a0-b5710b371248</a></p><p>Dedicated proportionate regulatory pathway for Niche fields</p><p>Article 5(5.g) requirements to the highest risk categories (Health institutions to create documentation for the products)</p><p>Update of MDCG guidance on In-house devices to better reflect the operational reality.</p><p>Off-label use and RUO are not falling on Article 5.5 so grey zone.</p><p> </p><p>Team-NB proposal for MDR &amp; IVDR - 5 topics on the agenda:  <a href="https://www.team-nb.org/nbs-views-on-mdr-and-ivdr-review-process/" rel="external nofollow noreferrer noopener" target="_blank">https://www.team-nb.org/nbs-views-on-mdr-and-ivdr-review-process/</a></p><p>Early dialogue: Use of this to talk to Notified Bodies</p><p>Article 61.10 &amp; WET: Update for more clarity. Narrow the scope.</p><p>Digitalisation: Machine readable documents, AI to support simulations to reduce Animal testing.</p><p>Coding for MD and IVD</p><p>Designation and recertification: For Notified Bodies</p><p>Breakthrough: Coordinated pathway with challenge to generate Clinical Data.</p><p>Notified Bodies Count - S New comers for MDR and IVDR: </p><p>SGS Fimko oy (IVDR 19): <a href="https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/notifications/1016921" rel="external nofollow noreferrer noopener" target="_blank">https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/notifications/1016921</a></p><p>ICIM S.P.A. (MDR 51) : <a href="https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/notifications?organizationRefeCd=EPOS_43747&amp;amp;filter=notificationStatusId:1" rel="external nofollow noreferrer noopener" target="_blank">https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/notifications?organizationRefeCd=EPOS_43747&amp;filter=notificationStatusId:1</a></p><p>Notice (MDR): <a href="https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/notifications/1020121" rel="external nofollow noreferrer noopener" target="_blank">https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/notifications/1020121</a></p><p><strong>Standards</strong></p><p>New Harmonized Standards - Clothing and sterilisers: <a href="https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202502078" rel="external nofollow noreferrer noopener" target="_blank">https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=OJ:L_202502078</a></p><p>Biocompatibility</p><p>ISO TS 23485: <a href="https://www.linkedin.com/posts/melazzouzi_iso13485-iso-medicaldevice-activity-7393773266689228801-d7LM?utm_source=share&amp;utm_medium=member_desktop&amp;rcm=ACoAAABZ07ABDocaBMTLJo8bsl8V3bgNSBIiZuI" rel="external nofollow noreferrer noopener" target="_blank">https://www.linkedin.com/posts/melazzouzi_iso13485-iso-medicaldevice-activity-7393773266689228801-d7LM?utm_source=share&amp;utm_medium=member_desktop&amp;rcm=ACoAAABZ07ABDocaBMTLJo8bsl8V3bgNSBIiZuI</a></p><p>UK Reliance with US FDA - Harmonization is ongoing: <a href="https://www.gov.uk/government/news/patients-to-benefit-as-uk-and-us-regulators-forge-new-collaboration-on-medical-technologies-and-ai" rel="external nofollow noreferrer noopener" target="_blank">https://www.gov.uk/government/news/patients-to-benefit-as-uk-and-us-regulators-forge-new-collaboration-on-medical-technologies-and-ai</a></p><p><strong>Service</strong></p><p>eIFU with free access -Test it and let us know : <a href="https://Easyifu.com" rel="external nofollow noreferrer noopener" target="_blank">https://Easyifu.com</a></p><p>eQMS for a structured Quality Management System - Get your demo: <a href="https://eqms-smarteye.com/" rel="external nofollow noreferrer noopener" target="_blank">https://eqms-smarteye.com/</a></p><p><strong>Magazine</strong></p><p>eMagazine . EMD Mag Free- Are Notified Bodies still the right model: <a href="https://easymedicaldevice.com/emd-mag/" rel="external nofollow noreferrer noopener" target="_blank">https://easymedicaldevice.com/emd-mag/</a></p><p><strong>ROW</strong></p><p>US FDA: Pre-RFD -:Combination product: <a href="https://www.fda.gov/media/189466/download" rel="external nofollow noreferrer noopener" target="_blank">https://www.fda.gov/media/189466/download</a></p><p>US FDA: QMSR guidelines -: How to create a QMS: <a href="https://www.fda.gov/media/189345/download" rel="external nofollow noreferrer noopener" target="_blank">https://www.fda.gov/media/189345/download</a></p><p> </p><p><strong>PODCAST</strong></p><p>Podcast review -  What happened in October 2025</p><p>Episode 357 - Highlights from La Rentrée du DM 2025: <a href="https://podcast.easymedicaldevice.com/357-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/357-2/</a></p><p>Episode 358 - Clinical Evidence under EU MDR - Why so many dossier fail (And how to fix it): <a href="https://podcast.easymedicaldevice.com/358-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/358-2/</a></p><p>Episode 359 - Real World Evidence - How to use it right for FDA and EU: <a href="https://podcast.easymedicaldevice.com/359-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/359-2/</a></p><p>Episode 360: US Government Shutdown - What FDA can still be doing? Rob Packard: <a href="https://podcast.easymedicaldevice.com/360-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/360-2/</a></p><p>Episode 361 - Automatisation of your QA RA Job with AI - Hatem Rabeh:  <a href="https://podcast.easymedicaldevice.com/361-2/" rel="external nofollow noreferrer noopener" target="_blank">https://podcast.easymedicaldevice.com/361-2/</a></p>
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33 MIN