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Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

382 episodios disponibles

Latest episodes of the podcast Medical Device made Easy Podcast

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Medical Device Software Versioning 21/08/2025

From Zero to One How to collaborate with clients 14/08/2025

From Zero to One: Becoming a Medical Device auditor 08/08/2025

From Zero to One – Should You Work with a QA/RA Recruiter? | Podcast Episode 31/07/2025

Why Switch to eIFU? Top Regulatory & Operational Benefits Explained for Medical Device Manufacturers 24/07/2025

Quality & Regulatory in MedTech – Interview with Pardeep Kaur 17/07/2025

From Zero to One: Creating your Consulting Firm 10/07/2025

Medical Device News JULY 2025 Regulatory Update 03/07/2025

From Zero to One: SaaS Founder’s First Five Years 25/06/2025

Notified Bodies raise concern on Risk Grading 18/06/2025

Software as a Medical Device: Beginner’s Guide to Testing & Validation 12/06/2025

Medical Device News JUNE 2025 Regulatory Update 04/06/2025

Trapped or Strategic? Changing Notified Bodies During MDR Transition 28/05/2025

How deepeye Medical overcame the AI ACT? 22/05/2025

Is EHDS dangerous for Medical Device manufacturers? 15/05/2025

When is Regulatory Affairs needed during Design? 07/05/2025

What is the new UK Post-Market Surveillance Requirements? 01/05/2025

How to register your Medical Device in Malaysia? 24/04/2025

Should you quit your job to become a consultant? 16/04/2025

How to satisfy Cybersecurity for FDA and EU? 10/04/2025

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