Medical Device made Easy Podcast
Listen Medical Device Regulation and Standards
Episodes
Managing Software Updates in Medical Devices: Best Practices & Pitfalls In the world of medical devices, software updates are never just technical tweaks—they directly impact patient safety, regulatory compliance, and […]
The post Medical Device Software Versioning appeared first on Medical Device made Easy Podcast. Monir El Azzouzi
From Zero to One: Mastering Client Collaboration in ConsultingStarting your consulting journey can feel overwhelming—finding clients, building trust, and delivering results all at once. In my conversation for the Medical […]
The post From Zero to One How to collaborate with clients appeared first on Medical Device made Easy Podcast. hamza benafqir
Have you ever wondered what it’s really like to work as a medical device consultant or ISO 13485 auditor? In this episode of the Medical Device Made Easy Podcast, I […]
The post From Zero to One: Becoming a Medical Device auditor appeared first on Medical Device made Easy Podcast. hamza benafqir
In our latest podcast, we dive deep into the recruitment world with Mitch, a founder and specialist recruiter in Quality Assurance & Regulatory Affairs (QA/RA). If you’re a hiring manager, […]
The post From Zero to One – Should You Work with a QA/RA Recruiter? | Podcast Episode appeared first on Medical Device made Easy Podcast. hamza benafqir
Everything You Need to Know About EU Regulation 2025/1234 and the Future of eIFU for Medical Devices On July 16, 2025, a pivotal regulatory update—EU 2025/1234—comes into effect, expanding the […]
The post Why Switch to eIFU? Top Regulatory & Operational Benefits Explained for Medical Device Manufacturers appeared first on Medical Device made Easy Podcast. hamza benafqir
Quality & Regulatory in MedTech – Interview with Pardeep Kaur Background: From IT in India to MedTech in Norway Day-to-Day as a QARA Manager First MedTech Role at Hy5Pro AS […]
The post Quality & Regulatory in MedTech – Interview with Pardeep Kaur appeared first on Medical Device made Easy Podcast. hamza benafqir
Guest: Stefan Bolleininger Title: From Zero to One: Creating your Consulting Firm Logo: Be on Quality Telling the story behind Be on Quality, Sharing also the life of a CEO […]
The post From Zero to One: Creating your Consulting Firm appeared first on Medical Device made Easy Podcast. hamza benafqir
Medboard: https://www.medboard.com/ EUROPE UK ROW Podcast
The post Medical Device News JULY 2025 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir
From Zero to One: SaaS Founder’s First Five Years with Ivan Perez Chamorro 🎧💡 In this exciting episode of the Easy Medical Device Podcast, we welcome Ivan Perez Chamorro, the […]
The post From Zero to One: SaaS Founder’s First Five Years appeared first on Medical Device made Easy Podcast. hamza benafqir
🎙️ Risk Grading Gone Wrong: How to Fix Your Severity, Occurrence & Detection Strategy Before Your Notified Body Does 🩺 Risk Management mistakes that could cost you your certification! In […]
The post Notified Bodies raise concern on Risk Grading appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Anindya Mookerjea will share with us his knowledge on Software Testing. We will review the basics and help you with being compliant to your projects.
The post Software as a Medical Device: Beginner’s Guide to Testing & Validation appeared first on Medical Device made Easy Podcast. hamza benafqir
episode 339 Medical Device
News JUNE 2025
Regulatory
Update monir el azzouzi easy medical device
The post Medical Device News JUNE 2025 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir
Who is Monir El Azzouzi? 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 […]
The post Trapped or Strategic? Changing Notified Bodies During MDR Transition appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Carmen Bellebna will share with us the journey of deepeye Medical to implement the EU AI act requirements in parallel with the EU MDR certification.
The post How deepeye Medical overcame the AI ACT? appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Cecile van der Heijden will disclose all the secret of the EHDS or European Health Data Space law.
The post Is EHDS dangerous for Medical Device manufacturers? appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Aouda Ouzza is helping us understand when the Regulatory Affairs person is needed during the design phase.
The post When is Regulatory Affairs needed during Design? appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Claire Dyson will clarify to us what is the new PMS requirements from UK MHRA.
The post What is the new UK Post-Market Surveillance Requirements? appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Adam Isaacs Rae is helping us to register our Medical Devices in Malaysia. We will review the requirements for it.
The post How to register your Medical Device in Malaysia? appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Yassine Bader will explain to you the advantage or the risk of quitting your permanent job to become a consultant.
The post Should you quit your job to become a consultant? appeared first on Medical Device made Easy Podcast. hamza benafqir
In this episode, Cyrille Michaud from MD101 will explain us how to prepare for Cybersecurity compliance for your medical device.
The post How to satisfy Cybersecurity for FDA and EU? appeared first on Medical Device made Easy Podcast. hamza benafqir
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