Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

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Avsnitt(406)

Why do you need an Initial Importer for the US Market?

Why do you need an Initial Importer for the US Market?

This is not anymore a question, you need an Importer for the US market. But what are the rules and who can do this. Stéphen Toupin from Dawa Medical will help us understand why your products are block...

13 Sep 20220s

Medical Device News: September 2022 Regulatory Update

Medical Device News: September 2022 Regulatory Update

Medical Device News is your summary of what happened in the Medical Device Field. I am providing you with the September 2022 Regulatory Update. Enjoy! The post Medical Device News: September 2022 Regu...

6 Sep 20220s

SaMD or SiMD – How to create your Design Dossier?

SaMD or SiMD – How to create your Design Dossier?

The Design Dossier of your Medical Device is really important. But what about a Software as a Medical Device. You will learn today some good practices to create them. The post SaMD or SiMD – How to cr...

30 Aug 20220s

New Blue Guide – What is the impact on Medical Devices?

New Blue Guide – What is the impact on Medical Devices?

The New Blue Guide is a guidance document that is really important to CE marking. And this has also some impact on the interpretation of the Medical Device legislation like EU MDR and IVDR. So don't m...

23 Aug 20220s

Why are we not Discontinuing your Products?

Why are we not Discontinuing your Products?

Why are you not discontinuing your products? I am not talking about just deleting the reference on your portfolio but obsoleting the documents linked to this product. The post Why are we not Discontin...

16 Aug 20220s

When you think “510k” but FDA says “DeNovo” with Spencer Jones

When you think “510k” but FDA says “DeNovo” with Spencer Jones

What would you think if you planned all your regulatory strategy for FDA 510k and when you submit, the FDA says to you that this should go DeNovo. Spencer Jones will tell us what he learned during thi...

9 Aug 20220s

How to create your Technical Documentation? [EU MDR and IVDR]

How to create your Technical Documentation? [EU MDR and IVDR]

I get a lot of messages about the creation of Technical Documentation and I want to share with you how I am doing it. Don't hesitate to check the link in the show notes for more details. The post How ...

2 Aug 20220s

Maybe you need a Cleanroom? Let’s check with Philippe Bourbon

Maybe you need a Cleanroom? Let’s check with Philippe Bourbon

The use of a cleanroom is something that depends on your products. Philippe Bourbon from the laboratory Icare will explain to us what exactly is needed to install and maintain cleanrooms. The post May...

26 Juli 20220s

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