ZARZA We are Zarza, the prestigious firm behind major projects in information technology.

Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

383 episodios disponibles

Latest episodes of the podcast Medical Device made Easy Podcast

Mostrando página 3 de 20

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

Medical Device News April 2025 Regulatory Update 04/04/2025

What if the Notified Body asks you: Is your Software Validated? 27/03/2025

What are the TOP 3 FDA inspection issues? 20/03/2025

Medical Device News March 2025 Regulatory Update 13/03/2025

How to avoid Clinical Investigation for your Device? 06/03/2025

FDA: Advantage of the Breakthrough Device Program 27/02/2025

How and Who to build your Risk Management File? 20/02/2025

The good, the bad and the ugly of certification bodies 13/02/2025

Medical Device News January 2025 Regulatory Update 06/02/2025

6 Tips to Grow as a QA RA Manager 30/01/2025

TOP 5 common NCs on an ISO 13485 audit 23/01/2025

How to perform your PMS for a Drug-Device Combination? 16/01/2025

How to register a Medical Device in South Africa? 09/01/2025

Medica: AI & MDR FLIP THE COIN 02/01/2025

Easy Medical Device Great Summary 2024 26/12/2024

What are the major pitfalls of Startups in Medical Devices? 19/12/2024

Medical Device News December 2024 Regulatory Update 12/12/2024

PCCP – The Magic tool for SaMD in the US? 05/12/2024

IEC 60601-1-8 How to test your Medical Device alarms? 28/11/2024

« Primera ‹ Anterior 1 2 3 4 5 ... 20 Siguiente › Última »