Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

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Episoder(404)

Software as a Medical Device: Beginner’s Guide to Testing & Validation

Software as a Medical Device: Beginner’s Guide to Testing & Validation

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 ...

12 Jun 20250s

Medical Device News JUNE 2025 Regulatory  Update

Medical Device News JUNE 2025 Regulatory Update

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 ...

4 Jun 20250s

Trapped or Strategic? Changing Notified Bodies During MDR Transition

Trapped or Strategic? Changing Notified Bodies During MDR Transition

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 […...

28 Mai 20250s

How deepeye Medical overcame the AI ACT?

How deepeye Medical overcame the AI ACT?

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 ove...

22 Mai 20250s

Is EHDS dangerous for Medical Device manufacturers?

Is EHDS dangerous for Medical Device manufacturers?

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 Me...

15 Mai 20250s

When is Regulatory Affairs needed during Design? 

When is Regulatory Affairs needed during Design? 

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 ...

7 Mai 20250s

What is the new UK Post-Market Surveillance Requirements?

What is the new UK Post-Market Surveillance Requirements?

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 ma...

1 Mai 20250s

How to register your Medical Device in Malaysia? 

How to register your Medical Device in Malaysia? 

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...

24 Apr 20250s

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