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Medical Device made Easy Podcast
Listen Medical Device Regulation and Standards
Medical Device News APRIL 2026 Regulatory Update
0 secs; April 01, 2026
These 3 podcasts will change how you see MedTech
0 secs; March 25, 2026
EUDAMED Deadline 2026 – 7 Steps Every MedTech Company Must Prepare
0 secs; March 18, 2026
Medical Device News March 2026 Regulatory Update
0 secs; March 12, 2026
IMDRF & Regulatory Reliance Explained: The Future of Global Medical Device Approvals
0 secs; March 04, 2026
IEC 60601 – From 2nd to 4th Edition: What Manufacturers Must Know
0 secs; February 25, 2026
Defect Management in SaMD — From Chaos to Control
0 secs; February 18, 2026
Medical Device News February 2026 Regulatory Update
0 secs; February 11, 2026
Validation & Supplier Management in MedTech
0 secs; February 04, 2026
QMSR Is Coming: Why FDA Inspections Will Change Completely in 2026
0 secs; January 28, 2026
How to Remediate a Design History File (DHF)
0 secs; January 21, 2026
Medical Device News January 2026 Regulatory Update
0 secs; January 14, 2026
Verification & Validation Explained — A Practical Conversation with Aaron Joseph
0 secs; January 07, 2026
Last Podcast of the Year – Easy Medical Device | Year in Review & What’s Next
0 secs; December 31, 2025
Simplifying EU Medical Device Regulations: Understanding the 2025 Proposal
0 secs; December 24, 2025
From Engineer to Clinical Evaluation Expert – The Journey of Florian Tolkmitt
0 secs; December 17, 2025
Medical Device News DECEMBER 2025 Regulatory Update
0 secs; December 10, 2025
How to become a LEAD AUDITOR made Easy
0 secs; December 03, 2025
What is changing with the new ISO 10993-1 version 2025
0 secs; November 26, 2025
From Zero to One: The journey of a CRO with Helene Quie
0 secs; November 19, 2025
Medical Device News November 2025 Regulatory Update
0 secs; November 12, 2025
Automatisation of your QA RA job with AI
0 secs; November 05, 2025
US Government Shutdown – What FDA can still be doing?
0 secs; October 29, 2025
Real-World Evidence (RWE): How to Use It Right for FDA and EU MDR Compliance
0 secs; October 22, 2025
Clinical Evidence under EU MDR – Why So Many Dossiers Fail (and How to Fix It)
0 secs; October 15, 2025
Highlights from La Rentrée du DM 2025
0 secs; October 08, 2025
Medical Device News OCTOBER 2025 Regulatory Update
0 secs; October 01, 2025
Post-Market Surveillance for Software and AI Devices
0 secs; September 24, 2025
From Surgeon to CEO: Building NEUROGYN AG Professor Marc Possover’s Journey
0 secs; September 17, 2025
Cybersecurity in Medical Devices – What QA/RA Must Do Today
0 secs; September 10, 2025
Medical Device News September 2025 Regulatory Update
0 secs; September 04, 2025
The good, bad and uglyof using AIfor QA RA Compliance
0 secs; August 27, 2025
Medical Device Software Versioning
0 secs; August 20, 2025
From Zero to One How to collaborate with clients
0 secs; August 14, 2025
From Zero to One: Becoming a Medical Device auditor
0 secs; August 07, 2025
From Zero to One – Should You Work with a QA/RA Recruiter? | Podcast Episode
0 secs; July 30, 2025
Why Switch to eIFU? Top Regulatory & Operational Benefits Explained for Medical Device Manufacturers
0 secs; July 23, 2025
Quality & Regulatory in MedTech – Interview with Pardeep Kaur
0 secs; July 16, 2025
From Zero to One: Creating your Consulting Firm
0 secs; July 09, 2025
Medical Device News JULY 2025 Regulatory Update
0 secs; July 02, 2025
From Zero to One: SaaS Founder’s First Five Years
0 secs; June 25, 2025
Notified Bodies raise concern on Risk Grading
0 secs; June 18, 2025
Software as a Medical Device: Beginner’s Guide to Testing & Validation
0 secs; June 11, 2025
Medical Device News JUNE 2025 Regulatory Update
0 secs; June 04, 2025
Trapped or Strategic? Changing Notified Bodies During MDR Transition
0 secs; May 28, 2025
How deepeye Medical overcame the AI ACT?
0 secs; May 21, 2025
Is EHDS dangerous for Medical Device manufacturers?
0 secs; May 14, 2025
When is Regulatory Affairs needed during Design?
0 secs; May 07, 2025
What is the new UK Post-Market Surveillance Requirements?
0 secs; April 30, 2025
How to register your Medical Device in Malaysia?
0 secs; April 23, 2025
Should you quit your job to become a consultant?
0 secs; April 16, 2025
How to satisfy Cybersecurity for FDA and EU?
0 secs; April 10, 2025
Medical Device News April 2025 Regulatory Update
0 secs; April 03, 2025
What are the TOP 3 FDA inspection issues?
0 secs; March 19, 2025
Medical Device News March 2025 Regulatory Update
0 secs; March 12, 2025
How to avoid Clinical Investigation for your Device?
0 secs; March 05, 2025
FDA: Advantage of the Breakthrough Device Program
0 secs; February 26, 2025
How and Who to build your Risk Management File?
0 secs; February 19, 2025
The good, the bad and the ugly of certification bodies
0 secs; February 12, 2025
Medical Device News January 2025 Regulatory Update
0 secs; February 05, 2025
6 Tips to Grow as a QA RA Manager
0 secs; January 29, 2025
TOP 5 common NCs on an ISO 13485 audit
0 secs; January 22, 2025
How to perform your PMS for a Drug-Device Combination?
0 secs; January 15, 2025
How to register a Medical Device in South Africa?
0 secs; January 08, 2025
Medica: AI & MDR FLIP THE COIN
0 secs; January 01, 2025
Easy Medical Device Great Summary 2024
0 secs; December 25, 2024
What are the major pitfalls of Startups in Medical Devices?
0 secs; December 18, 2024
Medical Device News December 2024 Regulatory Update
0 secs; December 11, 2024
PCCP – The Magic tool for SaMD in the US?
0 secs; December 04, 2024
IEC 60601-1-8 How to test your Medical Device alarms?
0 secs; November 27, 2024
How to build the perfect Quality Management System?
0 secs; November 20, 2024
Is FMEA bad for your Risk Management?
0 secs; November 13, 2024
How MDR and IVDR code can save you money?
0 secs; November 06, 2024
Medical Device News November 2024 Regulatory Update
0 secs; October 30, 2024
What does a strategy for regulatory compliance looks like?
0 secs; October 23, 2024
What are the TOP 3 issues on CAPAs?
0 secs; October 16, 2024
Medical Device News, October 2024 Regulatory Update
0 secs; October 09, 2024
How to select the best plastic for your Medical Device?
0 secs; October 02, 2024
UK vs EU vs US – How to switch to another region easily?
0 secs; September 23, 2024
How to do a PMCF Literature Search for Medical Devices?
0 secs; September 16, 2024
Medical Device News, Septembre 2024 Regulatory Update
0 secs; September 09, 2024
How to use AI GPT for your Quality and Regulatory work?
0 secs; September 05, 2024
How to go from Zero to Hero in Medical Devices?
0 secs; August 26, 2024
Manage the Transfer/Renewal/Surveillance/Change of your CE certificate
0 secs; August 19, 2024
How to use Harmonized Standards for Medical Devices?
0 secs; August 13, 2024
IVDR Class D – Lesson learned from Notified Bodies
0 secs; August 06, 2024
EU MDR Major update: Interruption or Discontinuation of supply!
0 secs; July 29, 2024
How to register your Medical Device in the UAE?
0 secs; July 22, 2024
EU Battery Regulation – How to be ready?
0 secs; July 15, 2024
AI Act – What are the challenges for Medical Devices?
0 secs; July 08, 2024
Medical Device News, July 2024 Regulatory Update
0 secs; July 05, 2024
How to submit your AI/ML SAMD the right way?
0 secs; June 24, 2024
AFNOR – How is a Notified Body designated?
0 secs; June 17, 2024
Cleaning Validation – How to select the worst case?
0 secs; June 10, 2024
Medical Device News June 2024 Regulatory Update
0 secs; June 05, 2024
Summative Evaluation – Common mistakes
0 secs; May 27, 2024
Are you more Corrections or Corrective Actions or Preventive Actions?
0 secs; May 20, 2024
How to select and evaluate your Contract Manufacturer?
0 secs; May 13, 2024
Quality Field Service for Medical Devices
0 secs; May 06, 2024
Medical Device NewsMAY 2024 Regulatory Update
0 secs; May 02, 2024
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