Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

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Avsnitt(403)

Post-Market Surveillance for Software and AI Devices

Post-Market Surveillance for Software and AI Devices

Post-Market Surveillance for Software & AI Devices – A QA/RA Guide Software evolves with updates. AI models may even change with real-world data. That makes Post-Market Surveillance (PMS) for digital ...

24 Sep 20250s

From Surgeon to CEO: Building NEUROGYN AG Professor Marc Possover’s Journey

From Surgeon to CEO: Building NEUROGYN AG Professor Marc Possover’s Journey

The journey from a successful surgical career to the leadership of a medical company is far from ordinary. Yet for Prof. Marc Possover, this evolution felt like a natural extension […] The post From S...

18 Sep 20250s

Cybersecurity in Medical Devices – What QA/RA Must Do Today

Cybersecurity in Medical Devices – What QA/RA Must Do Today

Cybersecurity in Medical Devices – A QA/RA Perspective Cybersecurity is often seen as an IT or engineering issue—but in reality, regulators and auditors turn to QA and Regulatory Affairs professionals...

10 Sep 20250s

Medical Device News September 2025 Regulatory Update

Medical Device News September 2025 Regulatory Update

Medboard EUROPE UK Switzerland Magazine Podcast: REST OF THE WORLD The post Medical Device News September 2025 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir

4 Sep 20250s

The good, bad and uglyof using AIfor QA RA Compliance

The good, bad and uglyof using AIfor QA RA Compliance

Artificial Intelligence is no longer just a buzzword — it’s already finding its way into Quality Assurance (QA) and Regulatory Affairs (RA) in the medical device industry. But what does […] The post T...

28 Aug 20250s

Medical Device Software Versioning

Medical Device Software Versioning

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, regulator...

21 Aug 20250s

From Zero to One How to collaborate with clients

From Zero to One How to collaborate with clients

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 conversa...

14 Aug 20250s

From Zero to One: Becoming a Medical Device auditor

From Zero to One: Becoming a Medical Device auditor

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: Beco...

8 Aug 20250s

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