Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

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Episoder(403)

From Zero to One: The journey of a CRO with Helene Quie

From Zero to One: The journey of a CRO with Helene Quie

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. This article […]...

20 Nov 20250s

Medical Device News November 2025 Regulatory Update

Medical Device News November 2025 Regulatory Update

MedBoard EU Service Magazine ROW PODCAST Social Media to follow The post Medical Device News November 2025 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir

12 Nov 20250s

Automatisation of your QA RA job with AI 

Automatisation of your QA RA job with AI 

Artificial Intelligence is reshaping the world of Quality and Regulatory Affairs.In this podcast episode, Hatem Rabeh joins to demystify how AI can be used — and where it must be […] The post Automati...

5 Nov 20250s

US Government Shutdown – What FDA can still be doing?

US Government Shutdown – What FDA can still be doing?

US Government Shutdown – What the FDA Can Still Be Doing? When the U.S. government experiences a shutdown, the consequences ripple across every industry — but for medical device manufacturers, […] The...

30 Okt 20250s

Real-World Evidence (RWE): How to Use It Right for FDA and EU MDR Compliance

Real-World Evidence (RWE): How to Use It Right for FDA and EU MDR Compliance

Real-World Evidence (RWE) is transforming how regulators evaluate medical devices — but many manufacturers still struggle to use it correctly. In this episode, we break down what RWE really means, […]...

23 Okt 20250s

Clinical Evidence under EU MDR – Why So Many Dossiers Fail (and How to Fix It)

Clinical Evidence under EU MDR – Why So Many Dossiers Fail (and How to Fix It)

Since the implementation of EU MDR 2017/745, clinical evidence has become one of the biggest challenges for medical device manufacturers — and a major source of Notified Body nonconformities. This […]...

16 Okt 20250s

Highlights from La Rentrée du DM 2025

Highlights from La Rentrée du DM 2025

The La Rentrée du DM 2025 conference brought together regulators, manufacturers, and industry experts to discuss the evolving landscape of European and global medical device regulation. Main themes in...

9 Okt 20250s

Medical Device News OCTOBER 2025 Regulatory Update

Medical Device News OCTOBER 2025 Regulatory Update

Medboard Europe Switzerland UK Magazine Events EasyIFU ROW Podcast Easy Medical Device Service Social Media to follow The post Medical Device News OCTOBER 2025 Regulatory Update appeared first on Medi...

1 Okt 20250s

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